Vehicle physical parameters.
\\n\\n
IntechOpen Book Series will also publish a program of research-driven Thematic Edited Volumes that focus on specific areas and allow for a more in-depth overview of a particular subject.
\\n\\nIntechOpen Book Series will be launching regularly to offer our authors and editors exciting opportunities to publish their research Open Access. We will begin by relaunching some of our existing Book Series in this innovative book format, and will expand in 2022 into rapidly growing research fields that are driving and advancing society.
\\n\\nLaunching 2021
\\n\\nArtificial Intelligence, ISSN 2633-1403
\\n\\nVeterinary Medicine and Science, ISSN 2632-0517
\\n\\nBiochemistry, ISSN 2632-0983
\\n\\nBiomedical Engineering, ISSN 2631-5343
\\n\\nInfectious Diseases, ISSN 2631-6188
\\n\\nPhysiology (Coming Soon)
\\n\\nDentistry (Coming Soon)
\\n\\nWe invite you to explore our IntechOpen Book Series, find the right publishing program for you and reach your desired audience in record time.
\\n\\nNote: Edited in October 2021
\\n"}]',published:!0,mainMedia:{caption:"",originalUrl:"/media/original/132"}},components:[{type:"htmlEditorComponent",content:'With the desire to make book publishing more relevant for the digital age and offer innovative Open Access publishing options, we are thrilled to announce the launch of our new publishing format: IntechOpen Book Series.
\n\nDesigned to cover fast-moving research fields in rapidly expanding areas, our Book Series feature a Topic structure allowing us to present the most relevant sub-disciplines. Book Series are headed by Series Editors, and a team of Topic Editors supported by international Editorial Board members. Topics are always open for submissions, with an Annual Volume published each calendar year.
\n\nAfter a robust peer-review process, accepted works are published quickly, thanks to Online First, ensuring research is made available to the scientific community without delay.
\n\nOur innovative Book Series format brings you:
\n\nIntechOpen Book Series will also publish a program of research-driven Thematic Edited Volumes that focus on specific areas and allow for a more in-depth overview of a particular subject.
\n\nIntechOpen Book Series will be launching regularly to offer our authors and editors exciting opportunities to publish their research Open Access. We will begin by relaunching some of our existing Book Series in this innovative book format, and will expand in 2022 into rapidly growing research fields that are driving and advancing society.
\n\nLaunching 2021
\n\nArtificial Intelligence, ISSN 2633-1403
\n\nVeterinary Medicine and Science, ISSN 2632-0517
\n\nBiochemistry, ISSN 2632-0983
\n\nBiomedical Engineering, ISSN 2631-5343
\n\nInfectious Diseases, ISSN 2631-6188
\n\nPhysiology (Coming Soon)
\n\nDentistry (Coming Soon)
\n\nWe invite you to explore our IntechOpen Book Series, find the right publishing program for you and reach your desired audience in record time.
\n\nNote: Edited in October 2021
\n'}],latestNews:[{slug:"webinar-introduction-to-open-science-wednesday-18-may-1-pm-cest-20220518",title:"Webinar: Introduction to Open Science | Wednesday 18 May, 1 PM CEST"},{slug:"step-in-the-right-direction-intechopen-launches-a-portfolio-of-open-science-journals-20220414",title:"Step in the Right Direction: IntechOpen Launches a Portfolio of Open Science Journals"},{slug:"let-s-meet-at-london-book-fair-5-7-april-2022-olympia-london-20220321",title:"Let’s meet at London Book Fair, 5-7 April 2022, Olympia London"},{slug:"50-books-published-as-part-of-intechopen-and-knowledge-unlatched-ku-collaboration-20220316",title:"50 Books published as part of IntechOpen and Knowledge Unlatched (KU) Collaboration"},{slug:"intechopen-joins-the-united-nations-sustainable-development-goals-publishers-compact-20221702",title:"IntechOpen joins the United Nations Sustainable Development Goals Publishers Compact"},{slug:"intechopen-signs-exclusive-representation-agreement-with-lsr-libros-servicios-y-representaciones-s-a-de-c-v-20211123",title:"IntechOpen Signs Exclusive Representation Agreement with LSR Libros Servicios y Representaciones S.A. de C.V"},{slug:"intechopen-expands-partnership-with-research4life-20211110",title:"IntechOpen Expands Partnership with Research4Life"},{slug:"introducing-intechopen-book-series-a-new-publishing-format-for-oa-books-20210915",title:"Introducing IntechOpen Book Series - A New Publishing Format for OA Books"}]},book:{item:{type:"book",id:"5493",leadTitle:null,fullTitle:"Escherichia coli - Recent Advances on Physiology, Pathogenesis and Biotechnological Applications",title:"Escherichia coli",subtitle:"Recent Advances on Physiology, Pathogenesis and Biotechnological Applications",reviewType:"peer-reviewed",abstract:"Escherichia coli is a versatile organism and very diverse. Members of this species vary from very pathogenic agents causing different types of diseases including meningitis, gastroenteritis, and septicemia, just to cite a few, to harmless organisms living in the intestines of both humans and animals. E. coli has also been used as a model organism for most bacteria except a few. For this reason, its study provides a huge advantage and can help understand the mechanisms involved in different processes such as pathogenesis, environmental disinfection, nutrient utilization, antibiotic resistance, and diagnostic/detection methods, and these are indeed the topics discussed in this book. The book has been divided into four main sections representing the different facets of E. coli applications, which include disease, biotechnology, environmental engineering and innovative approaches to detection, and lastly its physiology and cell biology. Such processes can be applied to the study of other organisms as well considering the development of diversity; for example, many organisms are capable of horizontal gene transfer, which is capable of increasing the fitness of the bacterial organisms involved and has a great impact on the control of such bacterial organism.",isbn:"978-953-51-3330-8",printIsbn:"978-953-51-3329-2",pdfIsbn:"978-953-51-4735-0",doi:"10.5772/63146",price:139,priceEur:155,priceUsd:179,slug:"-i-escherichia-coli-i-recent-advances-on-physiology-pathogenesis-and-biotechnological-applications",numberOfPages:434,isOpenForSubmission:!1,isInWos:null,isInBkci:!1,hash:"1ef47003dd99be6a53eaa91efb882dff",bookSignature:"Amidou Samie",publishedDate:"July 12th 2017",coverURL:"https://cdn.intechopen.com/books/images_new/5493.jpg",numberOfDownloads:53419,numberOfWosCitations:8,numberOfCrossrefCitations:65,numberOfCrossrefCitationsByBook:2,numberOfDimensionsCitations:126,numberOfDimensionsCitationsByBook:3,hasAltmetrics:1,numberOfTotalCitations:199,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"April 27th 2016",dateEndSecondStepPublish:"May 18th 2016",dateEndThirdStepPublish:"August 22nd 2016",dateEndFourthStepPublish:"November 20th 2016",dateEndFifthStepPublish:"December 20th 2016",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"52247",title:"Dr.",name:"Amidou",middleName:null,surname:"Samie",slug:"amidou-samie",fullName:"Amidou Samie",profilePictureURL:"https://mts.intechopen.com/storage/users/52247/images/5820_n.jpg",biography:"Dr. Amidou Samie is an associate professor of Microbiology at the University of Venda, in South Africa, where he graduated for his PhD in May 2008. He joined the Department of Microbiology the same year and has been giving lectures on topics covering parasitology, immunology, molecular biology and industrial microbiology. He is currently a rated researcher by the National Research Foundation of South Africa at the category C2 and has published widely in the field of infectious diseases and graduated several MSc and PhD students. His research activities cover mostly topics in infectious diseases from epidemiology to control. His particular interest lies in the study of intestinal protozoan parasites and opportunistic infections among HIV patients as well as the potential impact of childhood diarrhea on growth and child development. He also conducts research on water-borne diseases and water quality and is involved in the evaluation of point of use water treatment technologies using nanoparticles from silver and copper in collaboration with the University of Virginia in the USA. He also studies the use of medicinal plants for the control of infectious diseases as well as antimicrobial drug resistance.",institutionString:null,position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"3",totalChapterViews:"0",totalEditedBooks:"1",institution:null}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"1046",title:"Infectious Diseases",slug:"infectious-diseases"}],chapters:[{id:"54926",title:"Enterotoxigenic and Enterohemorrhagic Escherichia coli: Survival and Modulation of Virulence in the Human Gastrointestinal Tract",doi:"10.5772/intechopen.68309",slug:"enterotoxigenic-and-enterohemorrhagic-i-escherichia-coli-i-survival-and-modulation-of-virulence-in-t",totalDownloads:2089,totalCrossrefCites:0,totalDimensionsCites:1,hasAltmetrics:1,abstract:"Enterotoxigenic Escherichia coli (ETEC) and Enterohemorrhagic Escherichia coli (EHEC) are major food‐ and water‐borne pathogens that constitute a serious public health threat in low‐income and developed countries, respectively. Survival and expression of virulence genes in the human digestive tract are key features in bacterial pathogenesis, but the mechanisms behind these processes remain largely unknown due to obvious prohibition of human studies. Use of well‐controlled and multi‐parametric in vitro models can aid in addressing knowledge gaps in ETEC and EHEC pathogenesis. After a general description of the physiopathology of ETEC and EHEC infections, this chapter will give an overview of all the in vitro studies that have investigated the effect of the main physicochemical and biotic parameters of the human gut on pathogen survival and expression of virulence factors. We bring a picture of how ETEC and EHEC are able to adapt to each of the successive environments of the human gastrointestinal tract by reading many cues provided by both the host and the gut microbiota.",signatures:"Charlène Roussel, Charlotte Cordonnier, Valérie Livrelli, Tom Van de\nWiele and Stéphanie Blanquet‐Diot",downloadPdfUrl:"/chapter/pdf-download/54926",previewPdfUrl:"/chapter/pdf-preview/54926",authors:[{id:"120350",title:"Prof.",name:"Tom",surname:"Van De Wiele",slug:"tom-van-de-wiele",fullName:"Tom Van De Wiele"},{id:"191864",title:"Dr.",name:"Stéphanie",surname:"Blanquet-Diot",slug:"stephanie-blanquet-diot",fullName:"Stéphanie Blanquet-Diot"},{id:"191866",title:"Mrs.",name:"Charlène",surname:"Roussel",slug:"charlene-roussel",fullName:"Charlène Roussel"},{id:"191867",title:"Dr.",name:"Charlotte",surname:"Cordonnier",slug:"charlotte-cordonnier",fullName:"Charlotte Cordonnier"},{id:"197027",title:"Prof.",name:"Valérie",surname:"Livrelli",slug:"valerie-livrelli",fullName:"Valérie Livrelli"}],corrections:null},{id:"54475",title:"Virulence Factors and Innovative Strategies for the Treatment and Control of Uropathogenic Escherichia coli",doi:"10.5772/67778",slug:"virulence-factors-and-innovative-strategies-for-the-treatment-and-control-of-uropathogenic-i-escheri",totalDownloads:1549,totalCrossrefCites:2,totalDimensionsCites:4,hasAltmetrics:0,abstract:"Urinary tract infections (UTIs) are considered to be the most frequent bacterial infections. Escherichia coli is the major factor of community-acquired UTI (80–90%) and a large part of nosocomial UTI (30%), including cystitis, pyelonephritis, prostatitis, and asymptomatic bacteriuria. Uropathogenic E. coli (UPEC) shows a variety of virulence factors that allow their transition from the intestinal tract to the urinary tract and causing infection. The virulence factors responsible for pathogenesis outside the gastrointestinal tract belong to various functional groups. Antimicrobial resistance among E. coli causing UTIs is increasing in many countries around the world. This paper presents key virulence factors of UPEC such as adhesins, toxins, iron acquisition systems, and biofilm formation by UPEC, which are major problems in patients with long-term catheterization. The resistance of UPEC to antibiotics and innovative strategies of treatment and control of UPEC including drug therapy, preventive vaccines, probiotics, cranberry as source of antimicrobial metabolites, bacteriophages, new therapeutic antibiofilm treatment such as engineered phages, nanoparticles, and plant-derived antibacterial agents are also presented.",signatures:"Barbara Kot",downloadPdfUrl:"/chapter/pdf-download/54475",previewPdfUrl:"/chapter/pdf-preview/54475",authors:[{id:"189685",title:"Associate Prof.",name:"Barbara",surname:"Kot",slug:"barbara-kot",fullName:"Barbara Kot"}],corrections:null},{id:"56154",title:"The Pathogenesis of Escherichia coli Urinary Tract Infection",doi:"10.5772/intechopen.69030",slug:"the-pathogenesis-of-i-escherichia-coli-i-urinary-tract-infection",totalDownloads:3859,totalCrossrefCites:4,totalDimensionsCites:6,hasAltmetrics:1,abstract:"Urinary tract infections (UTIs) are the commonest human bacterial infections and are responsible for substantial morbidity and mortality, resulting in increased healthcare costs. Most UTIs are caused by specialized Escherichia coli (E. coli) strains referred to as uropathogenic E. coli (UPEC). UPEC possess a variety of virulence factors (VFs), which the organism uses to attach, invade, and injure the host. These VFs include adhesins, toxins, iron acquisition factors, lipopolysacharide capsules, and other invasins. Most studies on UTI pathogenesis have targeted VFs. The source of UPEC is the host’s fecal flora. According to the pathogenicity theory, UPEC strains with special VFs move from the host’s fecal flora to the urogenital tract and cause UTI. However, another theory states that the numerically abundant strain is responsible for UTI. Effective UTI management is hampered by the recent rise in antibiotic resistance, specifically, the recent emergence of multidrug-resistant E. coli sequence type 131. The distribution of VFs and other bacterial characteristics among different patient groups and UTI syndromes, is crucial understanding UTI pathogenesis, which would guide clinical decision making. For ST131 clonal group, further epidemiological studies are needed to clarify transmission pathways, risk factors for spread, and reservoirs, so that effective control measures can be devised.",signatures:"Timothy Kudinha",downloadPdfUrl:"/chapter/pdf-download/56154",previewPdfUrl:"/chapter/pdf-preview/56154",authors:[{id:"192136",title:"Dr.",name:"Timothy",surname:"Kudinha",slug:"timothy-kudinha",fullName:"Timothy Kudinha"}],corrections:null},{id:"54978",title:"Effect of Uropathogenic Escherichia coli on Human Sperm Function and Male Fertility",doi:"10.5772/intechopen.68312",slug:"effect-of-uropathogenic-i-escherichia-coli-i-on-human-sperm-function-and-male-fertility",totalDownloads:1579,totalCrossrefCites:1,totalDimensionsCites:4,hasAltmetrics:0,abstract:"Infections of the reproductive tract represent nearly 15% of male infertility cases. The most frequently isolated bacterium in the ejaculate of infertile men is Escherichia coli (E. coli), which causes between 60 and 85% of cases of chronic bacterial prostatitis leading to sperm damage. The aim of this chapter is to discuss the negative effects of E. coli on sperm quality and male fertility. The E. coli isolated from semen is uropathogenic (UPEC) and can damage sperm in different ways. UPEC induces activation of polymorphonuclear leukocytes with the release of cytokines and reactive oxygen species, the latter being harmful due to their ability to induce lipid peroxidation and early sperm capacitation. Also, UPEC decreases sperm motility, vitality and mitochondrial membrane potential through direct contact or mediated by its soluble metabolites. The negative effects are higher with strains with specific characteristics such as hemolytic capacity. In vivo studies with mice models have shown that UPEC inoculated into the epididymis induces inflammatory damage with testicular mass decrease and low sperm concentration. Future studies are needed to clarify the molecular mechanisms by which E. coli damages sperm. This knowledge will make it possible to take measures to avoid deleterious consequences on the fertilizing potential of men.",signatures:"Juana V. Villegas, Rodrigo Boguen and Pamela Uribe",downloadPdfUrl:"/chapter/pdf-download/54978",previewPdfUrl:"/chapter/pdf-preview/54978",authors:[{id:"191444",title:"Dr.",name:"Juana V.",surname:"Villegas",slug:"juana-v.-villegas",fullName:"Juana V. Villegas"},{id:"191447",title:"Dr.",name:"Rodrigo",surname:"Boguen",slug:"rodrigo-boguen",fullName:"Rodrigo Boguen"},{id:"192019",title:"Dr.",name:"Pamela",surname:"Uribe",slug:"pamela-uribe",fullName:"Pamela Uribe"}],corrections:null},{id:"54056",title:"Antimicrobial Mechanisms of Escherichia coli",doi:"10.5772/67363",slug:"antimicrobial-mechanisms-of-i-escherichia-coli-i-",totalDownloads:2534,totalCrossrefCites:3,totalDimensionsCites:3,hasAltmetrics:0,abstract:"Increasing antimicrobial resistance in strains of Escherichia coli is having a major impact on the healthcare industry worldwide. The appearance of extended-spectrum β-lactamase (ESBL) and carbapenem-resistant Enterobacteriaceae (CRE) strains has caused clinicians to worry that these strains might become as deadly as methicillin-resistant Staphylococcus aureus (MRSA) strains. It is vital that physicians have resources available to help keep them updated on these bacteria and the potential impact on healthcare. This chapter reviews the major strains of E. coli (intestinal and urinary), along with a review of the virulence factors, main diseases caused, and pertinent pathogenesis. The chapter then discusses antimicrobial therapy, what drugs are effective against these E. coli strains, and the development of resistance to these specific drug classes. Lastly, the molecular aspects of antimicrobial resistance mechanisms in this organism are discussed. This information will be especially helpful for physicians in providing them with a concise review of E. coli and an understanding of what is involved in antimicrobial resistance. Hopefully this information can be used to improve the outcomes for patients with E. coli infections.",signatures:"Wanda C. Reygaert",downloadPdfUrl:"/chapter/pdf-download/54056",previewPdfUrl:"/chapter/pdf-preview/54056",authors:[{id:"190201",title:"Dr.",name:"Wanda",surname:"Reygaert",slug:"wanda-reygaert",fullName:"Wanda Reygaert"}],corrections:null},{id:"54220",title:"Antibiotic Resistance among Escherichia coli: Isolates and Novel Approaches to the Control of E. coli Infections",doi:"10.5772/67400",slug:"antibiotic-resistance-among-i-escherichia-coli-i-isolates-and-novel-approaches-to-the-control-of-i-e",totalDownloads:2482,totalCrossrefCites:2,totalDimensionsCites:4,hasAltmetrics:0,abstract:"Bacteria are the microorganisms that most frequently cause infectious diseases in humans. The synthesis of silver nanoparticles (AgNPs) has attracted interest due to the new and different physical and chemical characteristics with applications in new fields. AgNPs, alone or supported on ceramic, are used as antimicrobial fillers in textiles and polymers for food-packaging and biomedical applications, for antimicrobial paints, and potentially for drug delivery. The evaluation of mesoporous nanostructures or nanocomposites as FDU-12/lignin/silver was effective in inhibiting Staphylococcus aureus, E. coli, Enterococcus faecalis, and Candida albicans. The best results were achieved against the inhibition of E. coli and with the structures FDU-12/silver. In plates with FDU-12/lignin/silver, FDU-12, FDU-12/lignin, and the positive control, it was enumerated at 0, 6, 14, and 27 colonies, respectively. While the development of resistance to a new antibiotic is expected, the time course and degree of resistance are uncertain and depend on various factors. The application of AgNPs as nanocomposites can alter the expression of bacterial proteins and could be used for inactivation. This review explores such aspects and a number of factors arising like the use of nanostructures against E. coli, from the knowledge acquired.",signatures:"Henrique C. Alves, Felipe de P. N. Cruz, Pamela C. P. de Assis, José D.\nC. Pessoa, Luis C. Trevelin, Angela M. de O. Leal and Cristina P. de\nSousa",downloadPdfUrl:"/chapter/pdf-download/54220",previewPdfUrl:"/chapter/pdf-preview/54220",authors:[{id:"192008",title:"Associate Prof.",name:"Cristina",surname:"Paiva De Sousa",slug:"cristina-paiva-de-sousa",fullName:"Cristina Paiva De Sousa"},{id:"192009",title:"Dr.",name:"Henrique",surname:"Cezar Alves",slug:"henrique-cezar-alves",fullName:"Henrique Cezar Alves"},{id:"192010",title:"Dr.",name:"Jose Dalton",surname:"Cruz Pessoa",slug:"jose-dalton-cruz-pessoa",fullName:"Jose Dalton Cruz Pessoa"},{id:"192011",title:"Prof.",name:"Luis Carlos",surname:"Trevelin",slug:"luis-carlos-trevelin",fullName:"Luis Carlos Trevelin"},{id:"192012",title:"Prof.",name:"Angela",surname:"Merici De Oliveira Leal",slug:"angela-merici-de-oliveira-leal",fullName:"Angela Merici De Oliveira Leal"},{id:"195264",title:"Dr.",name:"Felipe",surname:"de Paula Nogueira Cruz",slug:"felipe-de-paula-nogueira-cruz",fullName:"Felipe de Paula Nogueira Cruz"},{id:"195370",title:"BSc.",name:"Pamela Carla",surname:"Pereira De Assis",slug:"pamela-carla-pereira-de-assis",fullName:"Pamela Carla Pereira De Assis"}],corrections:null},{id:"53957",title:"E. coli as an Indicator of Contamination and Health Risk in Environmental Waters",doi:"10.5772/67330",slug:"-i-e-coli-i-as-an-indicator-of-contamination-and-health-risk-in-environmental-waters",totalDownloads:3035,totalCrossrefCites:6,totalDimensionsCites:10,hasAltmetrics:1,abstract:"Good public health depends on regular monitoring of water quality as faecal contamination is a serious problem due to the potential for contracting disease. Bacterial contamination in water is measured using indicator organisms, notably Escherichia coli and Enterococci which are used as primary indicators of contamination in fresh and marine water quality, respectively, rather than the total coliforms present. Although most E. coli and Enterococci strains cause only mild infections, their presence is indicative of the potential presence of other more pathogenic organisms which are a danger to human health. The acceptable levels of indicator organisms are defined in legislation and are set for drinking, river, well and marine water. This chapter will consider current gold standard culture methods of analysis for E. coli and compare them with molecular DNA procedures. Established culture methods use β‐D-glucuronidase to identify E. coli and β‐D-galactosidase to detect coliforms. Emphasis will be placed on newer procedures that can be used onsite supported by laboratory procedures used for confirmation. Available rapid fluorimetric procedures which have been developed for use in the field, based on the assay of β‐D-glucuronidase, will be discussed. The rapid advances in procedures using a molecular approach will be considered and compared with the more established methods for determining E. coli in water. It is essential that all these methods should be quantitative in order to comply with legal norms, and in this regard, the potential involvement of biosensor technology will be of great value in successfully transferring laboratory procedures to the field.",signatures:"Robert G. Price and Dirk Wildeboer",downloadPdfUrl:"/chapter/pdf-download/53957",previewPdfUrl:"/chapter/pdf-preview/53957",authors:[{id:"190960",title:"Prof.",name:"Robert",surname:"Price",slug:"robert-price",fullName:"Robert Price"}],corrections:null},{id:"55322",title:"Detection Methods for Lipopolysaccharides: Past and Present",doi:"10.5772/intechopen.68311",slug:"detection-methods-for-lipopolysaccharides-past-and-present",totalDownloads:3168,totalCrossrefCites:8,totalDimensionsCites:14,hasAltmetrics:0,abstract:"Lipopolysaccharide (LPS) is the primary component of the outer membrane of Gram‐negativebacteria. LPS aids in protecting bacterial cells, and also defines the unique serogroups used to classify bacteria. Additionally, LPS is an endotoxin and the primary stimulator of innate immune cells in mammals, making it an ideal candidate for early detection of pathogens. However, the majority of methods for detection of LPS focus on detection of the endotoxic component of the molecule, lipid A. Since lipid A is largely conserved among bacterial species and serogroups, these detection approaches are highly nonspecific. Thus, the importance of identifying the O‐polysaccharide antigenic portion of LPS, which confers serogroup specificity, has received a great deal of attention in recent years. However, methods that are highly selective to the O‐antigens are typically less sensitive than those that target the endotoxin. Here we present a history and comparison of the sensitivity of these methods and their value for detecting bacteria in a variety of different sample types.",signatures:"Loreen R. Stromberg, Heather M. Mendez and Harshini Mukundan",downloadPdfUrl:"/chapter/pdf-download/55322",previewPdfUrl:"/chapter/pdf-preview/55322",authors:[{id:"45308",title:"Dr.",name:"harshini",surname:"mukundan",slug:"harshini-mukundan",fullName:"harshini mukundan"},{id:"195105",title:"Dr.",name:"Loreen",surname:"Stromberg",slug:"loreen-stromberg",fullName:"Loreen Stromberg"},{id:"195106",title:"Mrs.",name:"Heather",surname:"Mendez",slug:"heather-mendez",fullName:"Heather Mendez"}],corrections:null},{id:"54599",title:"Effect of Environmental Conditions on Escherichia coli Survival in Seawater",doi:"10.5772/67912",slug:"effect-of-environmental-conditions-on-i-escherichia-coli-i-survival-in-seawater",totalDownloads:1421,totalCrossrefCites:2,totalDimensionsCites:5,hasAltmetrics:1,abstract:"We investigated separate and simultaneous effect of temperature, salinity and solar radiation, as well as bacterial strain and origin on Escherichia coli (E. coli) survival in seawater in experimental conditions. The experiments were carried out by placing the bottles filled with seawater of different salinity (15.0, 30.0 and 36.5 psu) and contaminated by bacterial cultures in three light‐protected air incubators set to different temperatures (6, 12, 18 and 24°C), or by placing the bottles in plastic containers filled with water of controlled temperature and exposing them to direct solar light. In experiments in the dark, two typed and two wild E. coli strains were tested. The mean T90 values were 33.55 h for E. coli ATCC 8739, 42.50 h for E. coli ATCC 35218, 72.8 h for E. coli originating from seagull feces and 278.6 h for E. coli originating from sewage, indicating differences between survival abilities among strains. The effect of temperature on T90 was significant only in seagull E. coli at 36.5 psu and sewage E. coli at 30.0 psu and was positive. The effect of salinity was significant only in seagull strain and also was positive. No interactive effect of temperature and salinity was recorded. Experiments in the presence of solar radiation, carried out with two ATCC E. coli strains, demonstrated its dominate harmful effect on bacterial cells, reducing T90 of both strains to 0.30–0.82 h for E. coli ATCC 35218 and 0.31–5.93 h for E. coli ATCC 8739. Within the ultraviolet A (UVA) and photosynthetically active radiation (PAR) spectrum of solar radiation, the wavelengths of 320–360 nm were found as most bactericidal. By comparing survival of cultivated E. coli cells to those in natural seawater samples, significantly higher survival E. coli cells in natural seawater samples was found.",signatures:"Slaven Jozić and Mladen Šolić",downloadPdfUrl:"/chapter/pdf-download/54599",previewPdfUrl:"/chapter/pdf-preview/54599",authors:[{id:"190668",title:"Dr.",name:"Slaven",surname:"Jozić",slug:"slaven-jozic",fullName:"Slaven Jozić"},{id:"193627",title:"Prof.",name:"Mladen",surname:"Šolić",slug:"mladen-solic",fullName:"Mladen Šolić"}],corrections:null},{id:"54411",title:"Isolation and Characterization of Escherichia coli from Animals, Humans, and Environment",doi:"10.5772/67390",slug:"isolation-and-characterization-of-i-escherichia-coli-i-from-animals-humans-and-environment",totalDownloads:6146,totalCrossrefCites:5,totalDimensionsCites:8,hasAltmetrics:0,abstract:"Working on a diverse species of bacteria that have hundreds of pathotypes representing hundreds of strains and many closely related family members is a challenge. Appropriate research design is required not only to achieve valid desired outcome but also to minimize the use of resources, including time to outcome and intervention. This chapter outlines basics of Escherichia coli isolation and characterization strategies that can assist in research designing that matches the set objectives. Types of samples to be collected, collection and storage strategies, and processing of samples are described. Different approaches to isolation, confirmation and concentration of various E. coli strains are summarized in this chapter. Characterization and typing of E. coli isolates by biochemical, serological, and molecular methods have been explained so that an appropriate choice is made to suite a specific E. coli strain/pathotype. Some clues on sample and isolate preservation for future use are outlined, and general precautions regarding E. coli handling are also presented to the researcher to avoid improper planning and execution of E. coli-related research. Given different options, the best E. coli research design, however, should try as much as possible to shorten the length of time to outcomes.",signatures:"Athumani Msalale Lupindu",downloadPdfUrl:"/chapter/pdf-download/54411",previewPdfUrl:"/chapter/pdf-preview/54411",authors:[{id:"185959",title:"Dr.",name:"Athumani",surname:"Lupindu",slug:"athumani-lupindu",fullName:"Athumani Lupindu"}],corrections:null},{id:"54927",title:"Escherichia coli Inactivation Using Pressurized Carbon Dioxide as an Innovative Method for Water Disinfection",doi:"10.5772/intechopen.68310",slug:"-i-escherichia-coli-i-inactivation-using-pressurized-carbon-dioxide-as-an-innovative-method-for-wate",totalDownloads:1437,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"Advanced water disinfection technologies that do not produce harmful by-products would be highly desirable. This study presents results for the use of pressurized carbon dioxide (CO2) and a liquid-film-forming apparatus for disinfection of seawater. The sensitivity of Escherichia coli to the pressurized CO2 was examined for various conditions of pressure, temperature, working volume ratios (WVRs), flow rates, and pressure cycling. Morphology of E. coli was observed by using scanning electron microscopy (SEM). A strong correlation between the E. coli inactivation efficiency and pressure cycling was detected (p < 0.001). The frequency and magnitude of pressure cycling were the key factors responsible for high rates of E. coli inactivation during the pressurized CO2 treatment. The results from linear regression analyses suggest that the model can explain about 91% of the E. coli inactivation efficiency (p < 0.001). The pressurized CO2 treatment (at 0.7 MPa, 20°C, 50% WVR) in the process involving pressure cycling (∆P = 0.12 MPa, 15 cycles) resulted in complete inactivation (5.2 log reduction) of E. coli within 3 min. These findings suggest that pressurized CO2 could be a potentially useful disinfection method for water treatment.",signatures:"Tsuyoshi Imai and Thanh-Loc Thi Dang",downloadPdfUrl:"/chapter/pdf-download/54927",previewPdfUrl:"/chapter/pdf-preview/54927",authors:[{id:"49754",title:"Prof.",name:"Tsuyoshi",surname:"Imai",slug:"tsuyoshi-imai",fullName:"Tsuyoshi Imai"},{id:"192033",title:"Dr.",name:"Thanh-Loc Thi",surname:"Dang",slug:"thanh-loc-thi-dang",fullName:"Thanh-Loc Thi Dang"}],corrections:null},{id:"54393",title:"Evaluating Meta-Analysis Research of Escherichia coli",doi:"10.5772/67337",slug:"evaluating-meta-analysis-research-of-i-escherichia-coli-i-",totalDownloads:1390,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"This chapter summarizes the progress in Escherichia coli research that used the meta-analysis approach. Using systematic searches for E. coli literature, we tracked meta-analysis publications and analyzed them based on a number of parameters. These included subject/topic (epidemiology, clinical/intervention/prevention and environmental), geographical region (the Americas, Europe and Australasia) and clinical syndrome (enteric, renal, and sepsis/meningitis). These parameters were plotted in terms of time span to obtain a sense of dynamic change or its absence through the years since the turn of the twentieth century. In terms of region, topic and syndrome, highest meta-analysis productivity was attributed to the Americas, clinical/intervention/prevention and enteric, all of which took place in the last 5 years (2011–2016). Over the combined time span of 16 years, the Americas significantly dominated meta-analysis outputs when compared to Europe and Australasia (P = 0.003). In conclusion, our findings facilitate awareness of the progress in this field wherein the studied parameters were analyzed for patterns over time and differential rates of publication productivity.",signatures:"Noel Pabalan, Eloisa Singian, Lani Tabangay and Hamdi Jarjanazi",downloadPdfUrl:"/chapter/pdf-download/54393",previewPdfUrl:"/chapter/pdf-preview/54393",authors:[{id:"190341",title:"Dr.",name:"Noel",surname:"Pabalan",slug:"noel-pabalan",fullName:"Noel Pabalan"},{id:"195013",title:"MSc.",name:"Eloisa",surname:"Singian",slug:"eloisa-singian",fullName:"Eloisa Singian"},{id:"195014",title:"Dr.",name:"Hamdi",surname:"Jarjanazi",slug:"hamdi-jarjanazi",fullName:"Hamdi Jarjanazi"},{id:"195015",title:"MSc.",name:"Lani",surname:"Tabangay",slug:"lani-tabangay",fullName:"Lani Tabangay"}],corrections:null},{id:"53916",title:"Escherichia coli as a Model Organism and Its Application in Biotechnology",doi:"10.5772/67306",slug:"-i-escherichia-coli-i-as-a-model-organism-and-its-application-in-biotechnology",totalDownloads:5619,totalCrossrefCites:10,totalDimensionsCites:30,hasAltmetrics:1,abstract:"Without a doubt, in the past 20 or so years, we have achieved the power of biology in different ways. In the present, we have many tools for developing novel technologies and applications for organism modifications that ultimately let us know many aspects of organisms’ biology and, therefore, apply that knowledge for technological purposes. Of all the model organisms and tools for genetic modification available, Escherichia coli stands out as a model organism and what we would like to call “molecular biologist tool box.” In the present chapter, we aim to review our current knowledge regarding genetic modifications and tools for modifying E. coli to generate plasmid vectors, single and multiple gene knockouts, whole genome editing, biosensor generation and applications and synthetic gene circuits and genomes.",signatures:"Vargas-Maya Naurú Idalia and Franco Bernardo",downloadPdfUrl:"/chapter/pdf-download/53916",previewPdfUrl:"/chapter/pdf-preview/53916",authors:[{id:"191984",title:"Dr.",name:"Bernardo",surname:"Franco",slug:"bernardo-franco",fullName:"Bernardo Franco"},{id:"191985",title:"Dr.",name:"Naurú Idalia",surname:"Vargas-Maya",slug:"nauru-idalia-vargas-maya",fullName:"Naurú Idalia Vargas-Maya"}],corrections:null},{id:"54261",title:"Biosensor Platforms for Rapid Detection of E. coli Bacteria",doi:"10.5772/67392",slug:"biosensor-platforms-for-rapid-detection-of-i-e-coli-i-bacteria",totalDownloads:6931,totalCrossrefCites:1,totalDimensionsCites:2,hasAltmetrics:0,abstract:"Risks of contamination with the well-known food pathogen Escherichia coli are increasing over the years. Therefore, rapid and portable technologies using different types of advanced devices named biosensors with various transduction capabilities (electrochemical, optical, or acoustic) were developed and seem to offer the most elegant solutions for research communities and final users-humans. Thus, integration of microfluidic biochips/biosensors into smartphones offer the real-time detection of any infection with E. coli, helping doctors in proceeding immediately with the clinical treatment. The present chapter will discuss about the analytical performances of biosensors and microfluidics such as selection of substrates, type of (bio)functionalization, low limit of detection, specificity, and response time for monitoring different E. coli strains. Thus, it is possible to rapidly identify (30–90 s) very low concentrations of E. coli (101 CFU/mL) down to a single bacterium in real samples (water, urine, milk, beef-meat) by simple integration of an angle scatter method and microfluidic-cellulosic pads (μPAD) loaded with micro-/nanoparticles functionalized with either polyclonal anti E. coli antibodies or with DNA strains into a portable device—a smartphone. Such biosensor configuration can also be used for the detection of other types of microorganisms with potential human and animal health concerns.",signatures:"Rodica Elena Ionescu",downloadPdfUrl:"/chapter/pdf-download/54261",previewPdfUrl:"/chapter/pdf-preview/54261",authors:[{id:"190834",title:"Associate Prof.",name:"Rodica",surname:"Ionescu",slug:"rodica-ionescu",fullName:"Rodica Ionescu"}],corrections:null},{id:"54674",title:"Essential Oils: The Ultimate Solution to Antimicrobial Resistance in Escherichia coli?",doi:"10.5772/67776",slug:"essential-oils-the-ultimate-solution-to-antimicrobial-resistance-in-i-escherichia-coli-i-",totalDownloads:1417,totalCrossrefCites:7,totalDimensionsCites:13,hasAltmetrics:1,abstract:"Antimicrobial resistance (AMR) is on the rise; the only solution for overcoming this is through accelerated drug discovery. At current, bacterial evolutionary rates is still clearly the undisputed winner in this war. To circumvent this, evolution of resistance need to be curbed and this can only be effective via novel approaches, one of which includes the use of a resistance modifying agent. The criterion to qualify as a resistance modifier necessitates the co-administration of the agent with an inhibitor that deactivates the bacterial resistance mechanism, restoring its original effectiveness. Natural products such as plant extracts and essential oils (EOs) have been viewed as a privileged group for investigation of their potential roles to combat antibiotic resistance, due to their compositions of active chemical compounds. The route for multidrug resistance development in Gram‐negative bacteria is primarily mediated by the sophisticated inner and outer membrane barriers, which function to protect the cell against external toxic compounds; hence, bypass of these bacterial membranes would successfully restore or improve efficacy of the antimicrobials. The aim of this chapter is to concisely describe some examples for recent strategies used in the screening of possible resistance modifiers from essential oils specifically against MDR Escherichia coli.",signatures:"Polly Soo Xi Yap, Shun Kai Yang, Kok Song Lai and Swee Hua Erin\nLim",downloadPdfUrl:"/chapter/pdf-download/54674",previewPdfUrl:"/chapter/pdf-preview/54674",authors:[{id:"190224",title:"Dr.",name:"Swee Hua Erin",surname:"Lim",slug:"swee-hua-erin-lim",fullName:"Swee Hua Erin Lim"},{id:"195385",title:"MSc.",name:"Polly Soo Xi",surname:"Yap",slug:"polly-soo-xi-yap",fullName:"Polly Soo Xi Yap"},{id:"195386",title:"BSc.",name:"Shun Kai",surname:"Yang",slug:"shun-kai-yang",fullName:"Shun Kai Yang"},{id:"221544",title:"Dr.",name:"Kok-Song",surname:"Lai",slug:"kok-song-lai",fullName:"Kok-Song Lai"}],corrections:null},{id:"54823",title:"Horizontal Gene Transfer and the Diversity of Escherichia coli",doi:"10.5772/intechopen.68307",slug:"horizontal-gene-transfer-and-the-diversity-of-i-escherichia-coli-i-",totalDownloads:1904,totalCrossrefCites:4,totalDimensionsCites:8,hasAltmetrics:1,abstract:"Escherichia coli (E. coli) strains are normal flora of human gastrointestinal tract. The evolution encoded by horizontally-transferred genetic (HGT) elements has been perceived in several species. E. coli strains have acquired virulence potential factors by attainment of particular loci through HGT, transposons or phages. The heterogeneous nature of these strains is because of HGT through mobile genetic elements. These genetic exchanges that occur in bacteria provide the genetic diversity.",signatures:"Maryam Javadi, Saeid Bouzari and Mana Oloomi",downloadPdfUrl:"/chapter/pdf-download/54823",previewPdfUrl:"/chapter/pdf-preview/54823",authors:[{id:"141443",title:"Prof.",name:"Mana",surname:"Oloomi",slug:"mana-oloomi",fullName:"Mana Oloomi"},{id:"191998",title:"Prof.",name:"Saeid",surname:"Bouzari",slug:"saeid-bouzari",fullName:"Saeid Bouzari"},{id:"191999",title:"MSc.",name:"Maryam",surname:"Javadi",slug:"maryam-javadi",fullName:"Maryam Javadi"}],corrections:null},{id:"53934",title:"Molecular Mechanisms of Phosphate Homeostasis in Escherichia coli",doi:"10.5772/67283",slug:"molecular-mechanisms-of-phosphate-homeostasis-in-i-escherichia-coli-i-",totalDownloads:2145,totalCrossrefCites:7,totalDimensionsCites:10,hasAltmetrics:0,abstract:"Life’s processes absolutely require inorganic phosphate for structural and energetic purposes. Escherichia coli has developed sophisticated mechanisms to acquire phosphate and to maintain intracellular amounts at optimal levels. The processes by which these simple cells maintain stable intracellular concentrations of phosphate are termed phosphate homeostasis, which involves mechanisms to balance the import, assimilation, sequestration, and export of phosphate. This chapter introduces the proteins involved in phosphate homeostasis and reviews information concerning the multiple phosphate transporters and the mechanisms by which they are regulated. It also introduces new concepts of how this bacterium responds to elevated extracellular levels of phosphate and presents a model for the integration of all of these processes to achieve homeostasis. The predominant importers are PitA, PitB, and the PstSCAB complex. Assimilation, or the incorporation of Pi into organic molecules, occurs primarily through the formation of ATP. Gene regulation relies on the PhoB/PhoR two-component system and the formation of a signaling complex at the membrane. The amount of intracellular phosphate can be fine-tuned through the formation or degradation of polyphosphate. Polyphosphate formation requires adequate supplies of ATP. In addition, when intracellular phosphate levels become too high, phosphate can be exported through PitA, PitB, or the YjbB transporters.",signatures:"William R. McCleary",downloadPdfUrl:"/chapter/pdf-download/53934",previewPdfUrl:"/chapter/pdf-preview/53934",authors:[{id:"191441",title:"Dr.",name:"William",surname:"McCleary",slug:"william-mccleary",fullName:"William McCleary"}],corrections:null},{id:"54277",title:"From Biology to Biotechnology: Disulfide Bond Formation in Escherichia coli",doi:"10.5772/67393",slug:"from-biology-to-biotechnology-disulfide-bond-formation-in-i-escherichia-coli-i-",totalDownloads:1600,totalCrossrefCites:1,totalDimensionsCites:2,hasAltmetrics:1,abstract:"Disulfide bonds formed between a pair of oxidized cysteines are important to the structural integrity and proper folding of many proteins. Accordingly, Nature has evolved several systems for the genesis and maintenance of such bonds. Beginning with the discovery of protein disulfide isomerase, which provided the first evidence for enzyme-catalyzed disulfide-bond formation, many years of research have resulted in the explication of the complex network of electron transport pathways needed for this process. Herein, we take a historical approach in describing the elucidation of disulfide-bond formation in E. coli. We frame this topic in the context of genome sequencing eras. The first section describes the discovery of eukaryotic protein disulfide isomerase and the subsequent research that followed from the early 1960s to the early 1990s, a time period we have named the pre-genomic sequencing era. The second section details the renaissance in research on disulfide-bond formation in the periplasm of prokaryotes, fueled by bacterial genetic screens and the development of genomic sequencing technology. Accordingly, we have named this section the genomic sequencing era, which ranges from the early 1990s to approximately 2010. The final section outlines the use of bacterial genetic screens to select for new oxidoreductase enzymes and their potential uses in biotechnological and pharmaceutical applications. This era we have dubbed the post-genomic sequencing era, and we envision it to represent the future of research on oxidative folding.",signatures:"Bradley J. Landgraf, Guoping Ren, Thorsten Masuch, Dana Boyd and\nMehmet Berkmen",downloadPdfUrl:"/chapter/pdf-download/54277",previewPdfUrl:"/chapter/pdf-preview/54277",authors:[{id:"190999",title:"Dr.",name:"Mehmet",surname:"Berkmen",slug:"mehmet-berkmen",fullName:"Mehmet Berkmen"}],corrections:null},{id:"54396",title:"Survival Strategy of Escherichia coli in Stationary Phase: Involvement of σE-Dependent Programmed Cell Death",doi:"10.5772/67672",slug:"survival-strategy-of-i-escherichia-coli-i-in-stationary-phase-involvement-of-e-dependent-programmed-",totalDownloads:1543,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"In a natural habitat, microbes respond to alterations in the amounts of nutrients or to stresses such as osmotic stress and stresses caused by low or high pH, salt, heat, and antibiotics by changing their mode for proliferation or survival. Similarly, Escherichia coli cells in a test tube change the growth mode according to environmental conditions when they enter a stationary phase. Until a sufficient supply of nutrients, the organism survives under such stressful and nutrient-limited conditions by altering gene expression to be more protective against such conditions. The definite trigger of the onset of stationary phase is still unclear, but several lines of evidence indicate that the regulation mechanism is very complicated and involves several transcriptional factors including alternative sigma factors, σE and σS. In addition, E. coli cells behave as a community of species and give rise to programmed cell death (PCD) for ensuring survival by controlling the cell number and supplying nutrients to sibling cells in long-term stationary phase (LTSP). The main PCD is probably performed by σE in E. coli. In this chapter, physiological functions of σE and PCD are introduced and reviewed and their possible involvement in survival mechanisms in stationary phase, especially LTSP, is shown.",signatures:"Tomoyuki Kosaka, Masayuki Murata and Mamoru Yamada",downloadPdfUrl:"/chapter/pdf-download/54396",previewPdfUrl:"/chapter/pdf-preview/54396",authors:[{id:"105925",title:"Prof.",name:"Mamoru",surname:"Yamada",slug:"mamoru-yamada",fullName:"Mamoru Yamada"}],corrections:null},{id:"54626",title:"Survival of Escherichia coli under Nutrient-Deprived Conditions: Effect on Cell Envelope Subproteome",doi:"10.5772/67777",slug:"survival-of-i-escherichia-coli-i-under-nutrient-deprived-conditions-effect-on-cell-envelope-subprote",totalDownloads:1577,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"In the aquatic ecosystems, microorganisms are exposed to seasonal and circadian cycles. Abiotic factors (e.g. low temperature, nutrient deprivation) can cause morphological and physiological changes in bacteria, thereby facilitating cell survival. While representing the interface between the cells and external environment, the cell envelope plays a major role in bacterial response to stress and characterization of the changes it undergoes can help to understand the adaptation process. In this study, analysis of the morphological and physiological changes as well as variations in protein composition of the Escherichia coli cell envelope was carried out for populations maintained for 21 days under nutrient deprivation and suboptimal temperatures (4°C and 20°C). It was found that the absence of nutrients led to a temperature-dependent reduction of cell culturability but had no effect on cell viability and integrity. The concentration of membrane proteins playing the key roles in cellular transport, maintenance of cell structure or bioenergetics processes remained mainly unchanged. In contrast, the level of several proteins such as the elongation factor EFTu 1, components of Bam complex or proteins implicated in chemotaxis was altered, thus indicating that cells were readily responding and adapting to stress.",signatures:"Maite Orruño, Claudia Parada, Vladimir R. Kaberdin and Inés Arana",downloadPdfUrl:"/chapter/pdf-download/54626",previewPdfUrl:"/chapter/pdf-preview/54626",authors:[{id:"190260",title:"Dr.",name:"Inés",surname:"Arana",slug:"ines-arana",fullName:"Inés Arana"},{id:"190272",title:"Dr.",name:"Maite",surname:"Orruño",slug:"maite-orruno",fullName:"Maite Orruño"},{id:"190273",title:"Dr.",name:"Claudia",surname:"Parada",slug:"claudia-parada",fullName:"Claudia Parada"},{id:"190275",title:"Dr.",name:"Vladimir",surname:"Kaberdin",slug:"vladimir-kaberdin",fullName:"Vladimir Kaberdin"}],corrections:null}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"},subseries:null,tags:null},relatedBooks:[{type:"book",id:"3092",title:"Anopheles mosquitoes",subtitle:"New insights into malaria vectors",isOpenForSubmission:!1,hash:"c9e622485316d5e296288bf24d2b0d64",slug:"anopheles-mosquitoes-new-insights-into-malaria-vectors",bookSignature:"Sylvie Manguin",coverURL:"https://cdn.intechopen.com/books/images_new/3092.jpg",editedByType:"Edited by",editors:[{id:"50017",title:"Prof.",name:"Sylvie",surname:"Manguin",slug:"sylvie-manguin",fullName:"Sylvie Manguin"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"825",title:"Current Topics in Tropical Medicine",subtitle:null,isOpenForSubmission:!1,hash:"ef65e8eb7a2ada65f2bc939aa73009e3",slug:"current-topics-in-tropical-medicine",bookSignature:"Alfonso J. Rodriguez-Morales",coverURL:"https://cdn.intechopen.com/books/images_new/825.jpg",editedByType:"Edited by",editors:[{id:"131400",title:"Prof.",name:"Alfonso J.",surname:"Rodriguez-Morales",slug:"alfonso-j.-rodriguez-morales",fullName:"Alfonso J. Rodriguez-Morales"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"799",title:"Salmonella",subtitle:"A Dangerous Foodborne Pathogen",isOpenForSubmission:!1,hash:"ba452d8a24ef16b1267d2854b28f6e6a",slug:"salmonella-a-dangerous-foodborne-pathogen",bookSignature:"Barakat S. M. Mahmoud",coverURL:"https://cdn.intechopen.com/books/images_new/799.jpg",editedByType:"Edited by",editors:[{id:"92016",title:"Dr.",name:"Barakat",surname:"Mahmoud",slug:"barakat-mahmoud",fullName:"Barakat Mahmoud"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"2068",title:"Understanding Tuberculosis",subtitle:"New Approaches to Fighting Against Drug Resistance",isOpenForSubmission:!1,hash:"077a11a53e4b135020092b8c1143f93c",slug:"understanding-tuberculosis-new-approaches-to-fighting-against-drug-resistance",bookSignature:"Pere-Joan Cardona",coverURL:"https://cdn.intechopen.com/books/images_new/2068.jpg",editedByType:"Edited by",editors:[{id:"78269",title:"Associate Prof.",name:"Pere-Joan",surname:"Cardona",slug:"pere-joan-cardona",fullName:"Pere-Joan Cardona"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"322",title:"Flavivirus Encephalitis",subtitle:null,isOpenForSubmission:!1,hash:"269535b3a2f21a46216f4ca6925aa8f1",slug:"flavivirus-encephalitis",bookSignature:"Daniel Růžek",coverURL:"https://cdn.intechopen.com/books/images_new/322.jpg",editedByType:"Edited by",editors:[{id:"33830",title:"Dr.",name:"Daniel",surname:"Ruzek",slug:"daniel-ruzek",fullName:"Daniel Ruzek"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"3842",title:"Leishmaniasis",subtitle:"Trends in Epidemiology, Diagnosis and Treatment",isOpenForSubmission:!1,hash:"861f3ca84eede677ba6cd863093d62f8",slug:"leishmaniasis-trends-in-epidemiology-diagnosis-and-treatment",bookSignature:"David M. Claborn",coverURL:"https://cdn.intechopen.com/books/images_new/3842.jpg",editedByType:"Edited by",editors:[{id:"169536",title:"Dr.",name:"David",surname:"Claborn",slug:"david-claborn",fullName:"David Claborn"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"1273",title:"Non-Flavivirus Encephalitis",subtitle:null,isOpenForSubmission:!1,hash:"fa857119b76ce546ccf16503e982a08e",slug:"non-flavivirus-encephalitis",bookSignature:"Sergey Tkachev",coverURL:"https://cdn.intechopen.com/books/images_new/1273.jpg",editedByType:"Edited by",editors:[{id:"62638",title:"Dr.",name:"Sergey",surname:"Tkachev",slug:"sergey-tkachev",fullName:"Sergey Tkachev"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"2061",title:"Salmonella",subtitle:"Distribution, Adaptation, Control Measures and Molecular Technologies",isOpenForSubmission:!1,hash:"64584b0d61f32814e0ed682bf052b088",slug:"salmonella-distribution-adaptation-control-measures-and-molecular-technologies",bookSignature:"Bassam A. Annous and Joshua B. Gurtler",coverURL:"https://cdn.intechopen.com/books/images_new/2061.jpg",editedByType:"Edited by",editors:[{id:"101172",title:"Dr.",name:"Bassam",surname:"Annous",slug:"bassam-annous",fullName:"Bassam Annous"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"971",title:"Malaria Parasites",subtitle:null,isOpenForSubmission:!1,hash:"d7a9d672f9988a6d5b059aed14188896",slug:"malaria-parasites",bookSignature:"Omolade O. Okwa",coverURL:"https://cdn.intechopen.com/books/images_new/971.jpg",editedByType:"Edited by",editors:[{id:"99780",title:"Prof.",name:"Omolade",surname:"Okwa",slug:"omolade-okwa",fullName:"Omolade Okwa"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"544",title:"Anemia",subtitle:null,isOpenForSubmission:!1,hash:"6b166fa7f2a834360680a40d0f170dc3",slug:"anemia",bookSignature:"Donald S. Silverberg",coverURL:"https://cdn.intechopen.com/books/images_new/544.jpg",editedByType:"Edited by",editors:[{id:"78753",title:"Dr.",name:"Donald",surname:"Silverberg",slug:"donald-silverberg",fullName:"Donald Silverberg"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}}],ofsBooks:[]},correction:{item:{id:"64875",slug:"erratum-introductory-chapter-primary-concept-of-hypoxia-and-anoxia",title:"Erratum - Introductory Chapter: Primary Concept of Hypoxia and Anoxia",doi:null,correctionPDFUrl:"https://cdn.intechopen.com/pdfs/64875.pdf",downloadPdfUrl:"/chapter/pdf-download/64875",previewPdfUrl:"/chapter/pdf-preview/64875",totalDownloads:null,totalCrossrefCites:null,bibtexUrl:"/chapter/bibtex/64875",risUrl:"/chapter/ris/64875",chapter:{id:"62932",slug:"introductory-chapter-primary-concept-of-hypoxia-and-anoxia",signatures:"Shrilaxmi Bagali, Gavishsidappa A. Hadimani, Mallanagouda S. Biradar and Kusal K. Das",dateSubmitted:"June 18th 2018",dateReviewed:"July 12th 2018",datePrePublished:"November 5th 2018",datePublished:"December 12th 2018",book:{id:"7009",title:"Hypoxia and Anoxia",subtitle:null,fullTitle:"Hypoxia and Anoxia",slug:"hypoxia-and-anoxia",publishedDate:"December 12th 2018",bookSignature:"Kusal K. Das and Mallanagouda Shivanagouda Biradar",coverURL:"https://cdn.intechopen.com/books/images_new/7009.jpg",licenceType:"CC BY 3.0",editedByType:"Edited by",editors:[{id:"187859",title:"Prof.",name:"Kusal",middleName:"K.",surname:"Das",slug:"kusal-das",fullName:"Kusal Das"}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"}},authors:[{id:"187859",title:"Prof.",name:"Kusal",middleName:"K.",surname:"Das",fullName:"Kusal Das",slug:"kusal-das",email:"kusaldas@yahoo.com",position:null,institution:null},{id:"188854",title:"Prof.",name:"M.S.",middleName:null,surname:"Biradar",fullName:"M.S. Biradar",slug:"m.s.-biradar",email:"editor.bjhs@bldeuniversity.ac.in",position:null,institution:null},{id:"263841",title:"Dr.",name:"Shrilaxmi",middleName:null,surname:"Bagali",fullName:"Shrilaxmi Bagali",slug:"shrilaxmi-bagali",email:"shrikots@yahoo.in",position:null,institution:null},{id:"265434",title:"Dr.",name:"Gavishiddappa A.",middleName:null,surname:"Hadimani",fullName:"Gavishiddappa A. Hadimani",slug:"gavishiddappa-a.-hadimani",email:"gavish.hadimani@yahoo.com",position:null,institution:null}]}},chapter:{id:"62932",slug:"introductory-chapter-primary-concept-of-hypoxia-and-anoxia",signatures:"Shrilaxmi Bagali, Gavishsidappa A. Hadimani, Mallanagouda S. Biradar and Kusal K. Das",dateSubmitted:"June 18th 2018",dateReviewed:"July 12th 2018",datePrePublished:"November 5th 2018",datePublished:"December 12th 2018",book:{id:"7009",title:"Hypoxia and Anoxia",subtitle:null,fullTitle:"Hypoxia and Anoxia",slug:"hypoxia-and-anoxia",publishedDate:"December 12th 2018",bookSignature:"Kusal K. Das and Mallanagouda Shivanagouda Biradar",coverURL:"https://cdn.intechopen.com/books/images_new/7009.jpg",licenceType:"CC BY 3.0",editedByType:"Edited by",editors:[{id:"187859",title:"Prof.",name:"Kusal",middleName:"K.",surname:"Das",slug:"kusal-das",fullName:"Kusal Das"}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"}},authors:[{id:"187859",title:"Prof.",name:"Kusal",middleName:"K.",surname:"Das",fullName:"Kusal Das",slug:"kusal-das",email:"kusaldas@yahoo.com",position:null,institution:null},{id:"188854",title:"Prof.",name:"M.S.",middleName:null,surname:"Biradar",fullName:"M.S. Biradar",slug:"m.s.-biradar",email:"editor.bjhs@bldeuniversity.ac.in",position:null,institution:null},{id:"263841",title:"Dr.",name:"Shrilaxmi",middleName:null,surname:"Bagali",fullName:"Shrilaxmi Bagali",slug:"shrilaxmi-bagali",email:"shrikots@yahoo.in",position:null,institution:null},{id:"265434",title:"Dr.",name:"Gavishiddappa A.",middleName:null,surname:"Hadimani",fullName:"Gavishiddappa A. Hadimani",slug:"gavishiddappa-a.-hadimani",email:"gavish.hadimani@yahoo.com",position:null,institution:null}]},book:{id:"7009",title:"Hypoxia and Anoxia",subtitle:null,fullTitle:"Hypoxia and Anoxia",slug:"hypoxia-and-anoxia",publishedDate:"December 12th 2018",bookSignature:"Kusal K. Das and Mallanagouda Shivanagouda Biradar",coverURL:"https://cdn.intechopen.com/books/images_new/7009.jpg",licenceType:"CC BY 3.0",editedByType:"Edited by",editors:[{id:"187859",title:"Prof.",name:"Kusal",middleName:"K.",surname:"Das",slug:"kusal-das",fullName:"Kusal Das"}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"}}},ofsBook:{item:{type:"book",id:"11253",leadTitle:null,title:"Sustainable Rural Development",subtitle:null,reviewType:"peer-reviewed",abstract:"\r\n\tThe quest to ensure sustainable rural development is at the human well-being in rural areas, peace and justice, good governance, and international partnership the decades-long quest to improve new development methods and sustainable approaches continues in our sustainability systems. Beginning with the UN and EU reports, most local Institutes of researches have set ambitious agendas for the rural community to increase the number of rural families saved by agriculture-related errors and preventable adverse events.
\r\n\tTo viable rural development has a vital role for rural communities. In the design of policies to be successful that affect them rural people have to decide and implement. According to this, it is a critical point to involve the poor and disadvantaged, along with related stakeholders, agricultural and rural development. Hence, for the sustainable development by international initiatives and all other institutions were searched and to be present the agricultural and related research results. To help support the effort, various governmental and non-governmental agencies established fundings for sustainable rural development research and fostered the development of human well-being goals in rural areas via national and international initiatives. In this context, most efforts resulted in successful cases. This book will intend to provide the reader with a comprehensive overview of the theory, approaches, strategies, and cases, and key elements and challenges of sustainable development, and Bioeconomy, Green and Circular economy for sustainability, and UN SDGs-Agenda 2030 and EU Green Deal.
\r\n\tI believe that this work will be fundamental in the field of SDG, and it will be a guiding, idea-generating key for researchers, practitioners, rural community, and policy decision-makers, and I hope that together we will establish sustainable rural life and development around the world.
\r\n\t
The internal combustion engine is a major contributor to greenhouse gas emissions and hydrocarbon pollution across the globe. Motor vehicles account for a major portion of pollutants such as carbon monoxide, nitrogen oxide, and volatile organic compounds [1]. Alternative powertrain vehicles (APVs), such as electric vehicles (EVs) and hybrid-electric vehicles (HEVs), are potential technological solutions to reduce transportation-sector emissions and fuel consumption. However, APVs require large amounts of battery-stored energy, which can be cost and weight prohibitive [2]. Degradation of the battery further adds to the lifetime cost of an APV, and battery degradation rate has been shown to be inversely correlated with fuel economy [3, 4]. Technologies that improve battery lifespan and fuel economy will reduce this lifetime cost and hasten the adoption of sustainable transportation.
Lithium-based batteries serve as the current main battery of choice for vehicle transportation because of their high energy density and ability for high cycle life. Improving cycle life of lithium batteries means limiting large currents in and out of the battery as much as possible to lower degradation and heat affects. Ultracapacitors (UC) can be added to vehicles to improve battery life by taking excess power away from the battery and storing it in temporary energy storage [5]. Capacitors can quickly unload power back into the system for high load situations such as a hard acceleration, taking away the need for a high-power drain from the battery.
This chapter will begin with a brief review of existing literature on empirical modeling of lithium-ion battery and ultracapacitor degradation. Then, a few select aging models will be reoriented for use in an APV energy management system (EMS). Finally, an example showing how to utilize these control-oriented models will be shown.
Aging of batteries is primarily caused by the formation of substrates in the chemical reaction pathways and the formation of cracks in the electrode materials from repeated stress cycles [6]. These aging mechanisms are accelerated by high charge and discharge rates, extreme battery temperatures, and deep depths of discharge [7]. Aging of the battery causes capacity fade (a decrease in the charge storage capacity) and power fade (a decrease in the battery efficiency). However, models of the cell chemistry that include the thermal and stress/strain relationships used to describe aging are computationally intensive and are ill-suited for use in APV EMSs [6, 8].
Research of battery aging in APVs instead tends to utilize empirical models [4, 9, 10, 11, 12, 13, 14]. Using empirical aging models for vehicle battery degradation analysis provides a good trade-off between precision and complexity. These empirical models do not consider the physical or chemical processes of the battery degradation but instead approximate the battery’s health by fitting experimental data to aging factors like charge throughput, calendar life, and number of charge/discharge cycles.
For instance, Refs. [9, 10, 15, 16] develop aging models that relate charge throughput to degradation, with temperature and current magnitude as additional stress factors. Refs. [17, 18] include depth of discharge as an additional stress factor, while [18] also distinguishes the impact of charging and discharging currents on battery degradation. The aging models for hybrid vehicle applications in [13, 14] consider a number of charge/discharge cycles and calendar life and use temperature, depth of discharge, and average state of charge as aging stress factors. Other models in the literature such as [8, 19, 20] use simple cycle counting to measure the state of health.
Current research works to integrate battery aging dynamics into these EMSs to form controllers that actively regulate battery degradation. In Ref. [4], the authors developed an SDP-based EMS for a parallel-HEV passenger vehicle that accounted for battery wear by mapping operating conditions to substrate growth, and associating substrate growth with battery state of health. The authors also analyzed how reducing battery aging increased the fuel consumption. In Refs. [4, 21], the authors developed a deterministic EMS for a parallel-HEV passenger vehicle that regulates battery degradation using a “severity factor” map: the control policy penalizes battery usage by an amount related to the severity of the operating conditions (in terms of temperature and current magnitude). The authors of [4] also showed an inverse correlation between the battery aging and fuel consumption.
Lithium batteries have a high energy density but low power density, meaning that although they store large amounts of energy, that energy cannot be accessed quickly. Additionally, high currents to and from the battery are a stress factor for battery degradation. A potential solution to these problems is to integrate UCs into the energy storage system. UCs store energy in the electric field of an electrochemical double layer and have a high power density but low energy, allowing them to serve as complements to battery energy storage [5]. By integrating UCs into the powertrain, it becomes possible to meet the vehicle power requirements with a smaller battery and reduce battery degradation by restricting the magnitude of the current going to or from the battery [5, 22]. Aging of UCs is primarily dependent on time, temperature, and cell voltage [23, 24, 25].
Current research is interested in optimal control and sizing of the UC to reduce battery aging [26], and in particular how battery aging and fuel economy are jointly impacted. Some related work includes Ref. [27], in which the authors develop an optimal control policy to govern UC behavior and demonstrate clear aging improvements over a passive (uncontrolled) system. Refs. [28, 29] carried out a parametric study on battery degradation versus UC size in EVs, using a rule-based control system to govern power allocation. Ref. [30] developed a control strategy integrating UCs with lead-acid batteries in a HEV for battery life extension, and found that a 50% increase in battery cycle life would be needed for the UC to be cost-effective. Ref. [31] experimentally demonstrated a decrease in battery power fade and temperature rise in lithium-ion batteries due to UCs on an EV load profile.
Meeting this goal of mitigating energy storage system degradation in APVs through control requires forming simplified models of the battery aging dynamics that can be included in or be used to generate an EMS. This chapter will summarize several approaches in the literature for using energy storage aging models for control applications.
Ref. [15] developed a lithium-ion battery empirical aging model for normalized battery capacity loss
This model of aging has been used for aging control in, for example, [3, 4, 12].
The Palmgren-Miner (PM) rule is a common method for analyzing fatigue life in mechanical systems and has been shown to effectively approximate the battery health over nonuniform charge and discharge cycles [8, 32, 33]. As per the PM rule, each charge and discharge cycle is considered to damage the battery by an amount related to the cycle life at that cycle’s depth of discharge, charge and discharge current, and temperature. Ref. [18], for instance, models the cycle life of a battery as a function of depth of discharge
Assume there is a charge-discharge cycle
For multiple charge and discharge cycles, the damage from each cycle can be added to find the total damage
Cumulative damage of zero denotes that the battery is unaged while cumulative damage of one means the battery has reached the end of its life. Typically, 20% capacity fade indicates a battery’s end of life. So,
However, the above method does not readily lend itself to use in control; full charge and discharge cycles can take a long time to develop, and the EMS must act at a faster rate. One possibility is that the energy management system could consider how its decision would cause the damage of the current cycle to grow or lessen. For instance, consider a battery to be at operating conditions
Then, Eq. (7) could be used in formulating an energy management strategy, such that the EMS would seek to minimize the additional damage caused by each decision it makes.
Ref. [23] provides the following model for ultracapacitor aging, where
where
This section develops a model for a hybrid energy storage system electric vehicle (HESS-EV)—specifically, an electric bus that uses a lithium-ion battery pack for energy storage and an ultracapacitor pack for handling large power requests. This example study will be used to show how active control of aging factors can improve the lifespan of the energy storage system without compromising energy consumption. This system is depicted in Figures 1 and 2.
HESS-EV model.
HESS-EV block diagram.
For this study, a backward-facing quasi-static vehicle model [34] is used to represent the vehicle dynamics. In this model, it is assumed that the driver accurately follows the velocity of a given drive cycle, eliminating the need for a driver model and allowing the time-history of the electrical load placed on the powertrain to be calculated in advance.
This vehicle model, illustrated in Figure 3, considers inertial forces, aerodynamic drag, and rolling resistance (note that road incline is neglected for this chapter). The drag force is given by
where
Vehicle diagram.
where
where
The inertial, drag, and rolling resistance forces sum together to give the traction force on the bus.
Parameter values for the vehicle model can be found in Table 1. The bus is assumed to be fully loaded and at its maximum allowable weight. Vehicle parameters are estimated from existing literature on bus simulation [35, 36, 37].
Parameter | Variable | Value |
---|---|---|
Vehicle mass | 18,181 kg | |
Frontal area | 8.02 m2 | |
Drag coefficient | 0.55 | |
Roll resistance coefficient | 0.008 | |
Wheel inertia | 20.52 kg-m2 | |
Motor inertia | 0.277 kg-m2 | |
Wheel radius | 0.48 m | |
Final drive ratio | 5.1:1 | |
Gearbox ratio | 5:1 |
Vehicle physical parameters.
This subsection describes the modeling of the HESS-EV powertrain, including the transmission, motor, battery, and ultracapacitor subsystems, as indicated in Figure 1. The goal of the vehicle model is to capture the primary forces on the vehicle while maintaining model simplicity. Both these make simulation of the system easier and make optimal control methods, such as dynamic programming or model-predictive control, less computationally complex. Otherwise, the energy management system might suffer from the “curse of dimensionality”.
Next, the vehicle speed and traction force are transformed into motor torque and motor speed. Assuming transmission efficiency of
and the motor speed is given by
Then, the mechanical power needed to drive the vehicle
Here, positive
The electrical power demand of the motor,
The efficiency map is obtained from the National Renewable Energy Laboratory’s Advanced Vehicle Simulator (ADVISOR) data library [38] and scaled to the appropriate size using the scaling method in [5]. It includes both the motor efficiency and the efficiency of the power electronics. The modeled vehicle utilizes a 250 kW AC induction motor.
The power demand for the electric motor is provided by battery power
Because
The previous subsections detailed how the driver’s electrical power request would be determined. As depicted in Figure 4, the EMS decides how that power is split between the lithium-ion battery and the ultracapacitor. This subsection will first detail the modeling of the battery, followed by modeling of the ultracapacitor.
Battery and UC block diagram.
This HESS-EV uses lithium-ion batteries represented by the simple battery model shown in Figure 5, where
Battery cell and battery pack equivalent circuit.
The equivalent resistance of the complete battery pack is given by
where
Using the equivalent circuit in Figure 4, the battery terminal voltage can be found from the OCV and battery power
Then, substituting Eq. (23) into Eq. (24) and solving yields
where
The parameters for the battery model can be found in Table 2. The number of cells in series was chosen so that the OCV would be in line with the recommendations in [40]. The number of cells in parallel was chosen so that the bus can be driven for 4 hours continuously to meet the power requirements of [40, 41].
Parameter | Variable | Value |
---|---|---|
Battery cells in parallel | 400 cells | |
Parallel sets in series | 100 sets | |
Total charge capacity | 340 Ah | |
Battery temperature |
Battery parameters.
For this example, the cycle counting method described in Eqs. (3)–(7) is used, with the aging model in Ref. [18] used to determine cycle life. This is illustrated in Figure 6. The battery is assumed to operate at a constant
Battery aging and dynamics block diagram.
The ultracapacitor model is similar in nature to the battery model, so the dynamics here will be presented more briefly. For this study, a second-order equivalent circuit based on the 100F ultracapacitor model in [42] is used to model the individual ultracapacitors. Parameters for this model are given in Table 3. Like with the battery, the ultracapacitor pack consists of ultracapacitors arranged in series and parallel as shown in Figure 7.
Parameter | Variable | Value |
---|---|---|
UC parallel cells | 100 | |
UC series sets | 100 | |
Resistor 1 | 29.6 mΩ | |
Capacitor 1 | 31.7 F | |
Resistor 2 | 14.7 mΩ | |
Capacitor 2 | 74.1781 F | |
Temperature |
Ultracapacitor parameters.
Ultracapacitor pack equivalent circuit.
As shown in Figure 1, the UC is connected to the DC bus through a converter, so that the voltage of the UC pack is independent of the voltage at the DC bus. The ultracapacitor pack takes on total power
Let
Then, substituting Eq. (23) into Eq. (24) and solving yields
The total charge in the capacitor
For this example, the cycle counting model in [23] and Section 3.3 is used. This is illustrated in Figure 8. The ultracapacitor is assumed to operate at a constant
Ultracapacitor aging & dynamics block diagram.
A deterministic dynamic programming (DDP) controller is used for the EMS. DDP is a form of optimal control—in this example, the DDP controller solves the following optimization problem over a known velocity profile that is
In plain terms, the DDP controller finds how to split power between the battery and ultracapacitor in such a way as to
Keep the UC charge near a target value
Minimize the aging of the battery
Ensure that the UC charge, UC power, and battery power stays within given bounds
The method to solve DDP problems can be found in Ref. [5].
In order to demonstrate the benefit of actively controlling aging, two versions of the controller will be tested:
Load-leveling DDP:
Active Aging Control: Battery power is unconstrained, but battery damage is directly penalized. A range of values are used for
The HESS-EV is simulated on the Manhattan Bus Cycle [43]—an urban bus velocity profile—for 4 hours at a time. After each simulation, the aging for the battery and ultracapacitor is measured. The battery capacity and ultracapacitor capacitances are then updated, and the next simulation begins. This process is repeated until the battery reaches its end of life.
The lifespan of the battery in years is estimated by measuring the total kilometers driven before the battery reached the end of its life, and then using the Federal Highway Administration’s average annual kilometers driven by transit busses [44] to convert the kilometers driven into an approximate number of years. Additionally, the ultracapacitor degradation and average kWh/km for the HESS-EV over the lifespan of the battery are measured.
Figure 9 shows a comparison between battery lifespan and fuel economy for both controller types. Clearly, the aging-aware control outperforms the load-leveling type controller: In all cases, the battery with actively-controlled aging has a longer lifespan.
Lifespan vs. fuel economy for HESS-EV, where
Additionally, this figure shows a trade-off between efficiency and battery lifespan: As the battery lifespan increases with greater penalties on battery damage, the energy efficiency of the vehicle drops. This is because greater penalties on aging cause more current to pass through UC in order to reduce the load on the battery. In turn, there are more power losses due to the internal resistances of the capacitor pack. This is illustrated in Figure 10, which shows the charge in the UC for two different values of
Ultracapacitor charge for two different values of
Figure 11 shows the relationship between battery degradation and ultracapacitor degradation. Two things are apparent: one, there is an inverse relationship between the two—increasing battery lifespan comes at the cost of reducing ultracapacitor lifespan. A cause of this can be observed in Figure 10. Second, ultracapacitor degradation happens much more slowly than battery degradation. Despite the battery reaching the end of its lifespan, the ultracapacitor ages no more than 6–11%.
Battery lifespan vs. UC aging.
Deterioration of energy storage systems is inevitable, but by understanding the process it becomes possible to control and slow the capacity and efficiency fade. This chapter covered empirical aging models for lithium-ion and ultracapacitor systems and their use in vehicle energy management. First, existing work on different lithium ion and ultracapacitor aging models was reviewed, as well as those models’ application in energy management control strategies. After reviewing aging models and discussing how to adapt empirical aging models for control, a case study was carried out on an ultracapacitor-augmented electric vehicle to show how actively controlling aging can improve an EMS. This case study included the steps necessary to model the vehicle and powertrain dynamics as well as simple or quasistatic models of the battery and ultracapacitor. DDP was generally used in two types of controllers: a load-leveling type controller that was unaware of aging dynamics, and a “smart” controller that incorporated battery aging dynamics into its design. When simulated, the aging-aware controller outperformed the simple controller, offering longer battery lifespan without any cost in fuel economy or vehicle performance. This demonstrates how advanced control—making EMSs aware of energy storage aging dynamics—can improve the efficiency and viability of alternative powertrain vehicles.
This work was supported by the University of California, Davis and by the Vertically Integrated Projects (VIP) program at UC Davis.
The authors declare no conflict of interest.
There is a great concern about the increase of elderly proportion follow-up the aging population process over the world. It is likely to create important macroeconomic issues and involve new policies challenges as it will put downward pressure on saving according to the life cycle hypothesis (LCH) prediction formulated by Modigliani and Brumberg [1]. Indeed, the saving decline is well recognized to be associated with lower rates of capital accumulation and growth in the economy. Saving is crucial for investment and the maintenance of strong and sustainable economic growth. In addition, saving is one of the essential aspects of building wealth and having a secure financial future. It gives a way out from uncertainties of life and enjoy a quality of life.
Hence, it is of great interest to look at the demographic changes impact on saving in order to seek how to prevent saving from such an eventual decline. The empirical studies in the topic, generally, have relied on the life cycle model; as it better explains the varying rates of savings in societies with relatively younger or older populations. However, the LCH’s prediction was not often empirically validated to argue that saving will be automatically depressed consequence of the population aging process. There is evidence that the social and economic conditions limit the scope of the LCH.
This study reviews the LCH to emphasize the most significant factors that may distort its prediction. It focuses on the uncertainty to explain the aging-saving relationship. It tries to check empirically whether uncertainty consideration may distort the LCH. Thereby the aging population do not put a down pressure on saving systematically.
However, given the difficulty to directly and objectively estimate uncertainty extent on saving behavior, we indirectly capture by an auxiliary variable the unemployment. We seek to highlight the influence of the precautionary motive related to the risk of unemployment. Thus, we try to give information about the transmission mechanism between aging population and saving considering the unemployment savings pattern as a determinant of saving behavior in a setting of unavailability of unemployment allowance. So, we draw attention that unemployment is an important factor up to distort the life cycle model’s prediction.
Unlike previous studies, we build our estimates not only on the total dependency ratio (the proportion of population aged less than 15 years and aged 60 years or more versus the proportion aged 15–59) as an aging indicator, but also on the old-age dependency ratio (the proportion of population aged 60 years or more versus the proportion aged 15–59). This will allow us to make comparison and to deduce the effect of the child dependency ratio (the proportion of population aged less than 15 years versus the proportion aged 15–59). Besides, we focus on national saving to avoid narrowing the population aging impacts since the corporate and the government saving are sensitive to population aging as the household saving.
In addition, given the lack of researches on this issue on developing countries (which economic and social environment greatly differ from the developed countries) we devote our study to Tunisian case. Tunisia is an interesting case of study because it is a well advanced in the aging process. As well, it suffers from an enduring and high unemployment rate and an inefficient pension system (as detailed in Section 3). Furthermore, it is characterized by a strong altruistic familial intergenerational relationship [2, 3, 4].
To check out the relationship between aging, unemployment, national saving and economic growth we apply a time series modeling approach over the period 1970–2019. We carry out a Structural VAR model, as defined by Sims [5]. We analyze the impulse response functions (IRFs) of different shocks for all variable’s fluctuations. We also apply the bootstrap methods to construct the confidence intervals of the IRFs. Additionally, we complete our dynamic analysis by the variance decomposition.
This study represents the first attempt to model the Tunisian aggregate national saving by considering both the impact of demographic changes and of unemployment.
In what follows, we give, in Section 2, an overview of the life cycle hypothesis and its bounds. In Section 3 we give some sight of the demographic change and the saving evolution occurred in Tunisia. In Section 4, we specify the econometric model and in Section 5 we discuss the results found. Finally, we end, in Section 6, with the main findings and policy recommendations.
In this section we state the life cycle’s savings to emphasize the social and economic conditions that may constrain its validation.
The life cycle theory pinpoints the intertemporal allocation of time, effort and money. In its simple form, the standard life cycle hypothesis’s (LCH) formulated by Modigliani and Brumberg [6], suggests that individuals save during working life for their consumption needs when they retire, dissave after retirement, and die without wealth. Hence, individuals will smooth consumption over their lifetime regard to the expected lifetime resources. They accumulate wealth during the pre-retirement period by consuming less than their disposable income. So, during retirement, they de-cumulates wealth to finance its consumption. That is, the saving rate should follow a hump-shaped over the life cycle as shown by the Figure 1 (in the Appendix).
Therefore, one very important implication of the LCH is that the demographic profile of a population should be an important factor influencing the aggregate saving rate. Given that population aging is defined as a shift in the population age distribution towards old age, so a change of the balance between youth and elderly proportion (defined in the following as a person aged over 60 years-old) causes society to age and subsequently to affect the saving pattern.1 Such a change may change the savers proportion in the economy and diminish the aggregate saving rate according to the LCH.
If there is a large proportion of the population working, then, the saving rate should be high. However, if there is a large population proportion over retirement age or very young, the saving rate would be low. This suggests that aggregate saving rate should be negatively correlated with total dependency ratio.
Even though the theoretical conclusion of the life cycle model is clear, the empirical evidence is not often proved and stays controversial until today as it was decades ago. There is evidence that elderly may not dissave, at least not to the extend hypothesis suggested by the pure life cycle model which abstracts a number of factors that would complicate its prediction.
The Life cycle theoretical conclusion is understandable given its simplifying assumptions such as no uncertainty, a finite decision horizon, no inheritance and perfect financial market with no credit constraint [7]. According to the LCH, individual takes decisions basically depending to events and fact that are known with certainty in each period of life (such future income, death date, and interest rate). Nevertheless, these assumptions are considered too restrictive. Indeed, events are uncertain [8, 9] and financial market is imperfect with credit constraint. Uncertainty affects consumption and savings behavior as consumers are generally cautious. Moreover, according to the Kotlikoff [10] dynastic model of savings, individuals do not act in a finite horizon, but in an infinite one. In addition, they have a dynastic behavior characterized by a strong preference to let, at their death, a very limited capital de-cumulation [11, 12, 13]. Thus, parents, having an altruistic motive, seek to not decumulate wealth to leave inheritance to their children. Consequently, the population aging may not automatically depress national saving. Kotlikoff and Summers [14] conclude that the “life cycle saving” cannot account for more than 20 percent of U.S. capital formation, and the intergenerational transfers play a dominant role in wealth accumulation, accounting for 80 percent or more of observed wealth.
Additionally, it is worth noting that the conflicting evidence on the life cycle saving may also be due to the econometric approaches used and the aging indicator chosen. Indeed, the micro econometric analysis invalidates life cycle model’s prediction to support the Kotilkoff hypothesis but their results are difficult to aggregate because of severe problem of heterogeneous behavior at the household level. Conversely, studies based on macro data for a country generally support the prediction. However, most of them refer to developed societies while in developing societies people face different economic challenges and social conditions, which may lead to different evidences. In that way, these studies could not be very useful for understanding saving behavior in developing countries. The difference through countries is in the design of pension systems and health care, taxes and transfers as well as labour market conditions, which are unavoidably depend to the population age distribution. As well, they may alter individual economic behavior and so could be the origin of the inconsistency LCH’s evidences.
Also, the choice of the population aging indicator to estimate is crucial. The total dependency ratio which is generally used does not accurately reflect the aged population since it composed of both the old and the child dependency ratio. It is more fitting to use the old-age dependency ratio to explicitly consider the effect of aged population on savings rate [15]. With more cautious in the aging indicator use, the life cycle model’s prediction is likely to be endorsed also in macroeconomic approach.
The LCH analysis has been gradually enriched, to focus on three reasons for accumulation: the foresight for retirement, the intergenerational altruism and inheritance and the wariness of the saver face to risk (of income, health and lifetime span). In this work, we focus more on the third reason of accumulation by looking at how uncertainty, about future income affects the behavior of the individual’ saving. Uncertainty consideration has made it possible to highlight precautionary behavior as the future work income is random; consumption (otherwise savings) depends not only on expectation, but also on the variance of the expected income. A risk-averse or aware consumer will save more. In fact, savings play an insurance role against the hazards affecting the household, especially the hazards related to income (unemployment, loss of wages, etc.) [16]. Thus, uncertainty about future income affects the behavior of the individual ‘saving by increasing the demand for precautionary assets, and hence savings amount.
As well, there is precautionary behavior as to face health care expenditure at advanced aged when the risk of health problems is potentially great; notably in the context of inefficient health care system [17]. As a result, households are saving not only to offset lower future income, but also to insure against all sorts of risks.
However, empirically it is not easy to estimate uncertainty extent on saving behavior. It is difficult to quantify this relationship given the difficulty to directly and objectively estimate uncertainty. Empirically there are no quantitative measurements of uncertainty that could be used directly. In the case studies, income uncertainty is usually measured indirectly by auxiliary variables such as inflation rate, unemployment rate or a derivative of these variables. In this case of study, we focus on unemployment as an income uncertainty indicator to better understand the aging impact on saving and to find an answer to the crucial question: do population aging depress savings?
Unemployment inevitably alters the savings behavior by its two aspects: (1) a high rate and (2) an increase in the average age of unemployed [18].
(1) The high and persistent unemployment rate weights on household confidence, prompting them to increase their precautionary savings. Such behavior is accentuated in a setting of unavailability of unemployment allowance (like in Tunisia) [19]. Thus, for precautionary reasons and to finance unexpected income losses, unemployment is viewed as an income uncertainty given the probability to become unemployed alters the savings behavior. Faure et al. [20] shown that unemployment and the deterioration of household confidence accounted for almost 20% of the aggregate consumption decline.
(2) The increase of the unemployed average age implies that the working population becomes occupied at advanced age. Consequently, they would save a less amount of wealth and they would form a low retirement pension. To offset at this lack of savings they do not immediately dissave at the beginning of the retirement. They would even compensate their low pension by working further after retirement, mainly at the beginning of the period (as long as they stay in better health) to face the future’ uncertainties. Also, given the granting difficulties for credit liquidity at the retirement period, this insufficient pension nudges them to continue to save to keep up a certain level of consumption. It increases, in addition, the need for retirement savings from private sources.
Furthermore, the high and enduring unemployment increases inter-vivos transfers, which represents a form of precautionary saving [21]. With a dynastic behavior (which is ignored by the LCH) the old generation (parents) saves more throughout the life cycle to help the young generation (their offspring) to facing uncertainty and hard-economic conditions related for instance to unemployment’s conditions. Thus, if intergenerational transfers (by purely altruistic incentive or following a kind of implicit contract between parents and children) are an important motive for savings; elderly rarely decumulate their wealth.
Henceforth, given uncertainty about the future income and lifespan, liquidity constraints, and the wish to leave bequests (a dynastic savings) population aging would not drive the decrease of savings. Therefore, aging economic impact on the household saving and so on the cumulative and on national saving, may not be large [22].
Hence, for our empirical evaluation of the life cycle hypothesis, we analyze the aging-savings relationship in a developing country, in particular, Tunisia. It greatly differs, economically and socially, from the developed countries, by its altruistic familial intergenerational relationship, the enduring and high unemployment rate and the inefficient pension system; as detailed in the section below.
Tunisia after has shortly ended its demographic transition regime, it has well undertaken the population aging process. During the period 1960–2019, the mortality rate fell from 35 to 40 per thousand to a low rate 5.9. Likewise, fertility which was nearby 8 children per woman fell to 2.17. Thus, the life expectancy has attained an average close to that of developed countries 75.4 years (78.1 years for woman and 74.5 years for man) in 2017.
Accordingly, the population age distribution has shifted towards aging. This fertility decline has narrowed the bottom of the age pyramid by the decline of the younger generation size, while the mortality decline has enlarged the top of the pyramid through the life expectancy gain. Thus, the age range proportion less than 15 years-old becomes less important (passing from 46.5 percent to 24.7) and it is likely to continue its decline. In the contrary, a remarkable increase is recorded for the proportion of person aged over 60 years-old (from 5.5 percent to 12.6) and is expected to increase by 10 points over the future three decades. Therefore, during 1966–2019, the child dependency ratio has sharply declined (from 96.27 percent to 39.36) while the old-age dependency ratio has increased (from 11.60 percent to 20.08). Consequently, the total dependency ratio has decreased (from 107.86 percent to 59.44).
Tunisian economy recorded a high and enduring unemployment. Over the period 1966–2000, it has increased by 6.1 points to pass from 12.5 percent to 18.6, and then fell slightly to stabilize during the last two decades (2000–2019) around 15.3 percent. Additionally, aging has hit the age composition of the unemployed. Indeed, the modal age range of the unemployed population has moved from less than 25 years-old (by about 29 percent) to 25–29 years-old (by about 34.2 percent) during 2005–2011. It is worth noting here that Tunisian authorities do not distribute any unemployment allowance.2
For the national saving, it has evolved with some fluctuations. During the period 1970–2010, the national saving rate (of gross national disposable income) was relatively stable around an average of 22.8 percent then progressively fell to achieve 9.3 in 2019, mainly due to a steady loss of purchasing power.3
According to the Islamic Development Bank, the behavior of Tunisian investors appears to be driven by factors related to consumer demand and/or the income effect [23]. The financial changes in interest rates have more effect on the savings structure than on its volume. Indeed, the financial liberalization policy adopted (since the structural adjustment plan in 1986) has not succeeded to stimulate private savings through the increasing of the real interest rates [24]. In Tunisia, saving behavior seems to comply more to the Keynesian approach.
However, an interest for the long-term financial savings is recorded. During 2010–2017, the listed companies increase from 56 to 81 with a broad sectors diversification. Likewise, the life insurance, as a long-term saving vehicle, has undergone an important increase; the average annual growth rate was 18 percent in 2017. Its share in the insurance market has climbed from 12.05 percent in 2009 to 20.2 in 2017; however, it remains far from the international standards (about 56.2 percent).
This interest for the long-term savings is explained by the failure of the pension system the pay-as-you-go system and the bankruptcy of the provident fund as well as the authority’s future intention to withhold a proportion of the retirement pension.4 Thus, the insured people are driven to form a complementary retirement pension under others retirement savings forms through voluntarily paying into saving schemes in private financial institutions. This savings form is encouraged by the financial authority through the establishment of tax benefits.
Concerning the non-financial savings, it is allocated to buy housing, jewelry or land by household and productive assets by individual corporate. Household saving is particularly oriented to housing savings which has experienced a growth rate of about 5.5 percent during 2000–2017.
To look at the relationship between population aging and savings in an unemployment context in Tunisia over the period 1970–2019, we apply a structural VAR model, as defined by Sims [25]. This enables us to approach a multivariate causal setting allowing the coexistence of both short and long-term forces derived from the aging influences on saving decisions. Finally, we deepen our dynamic analysis by application the techniques of impulse response functions (IRFs) of different shocks for all variable’s fluctuations and of the variance decomposition (VDC).
To undertake the aggregate saving model estimating, we use as an independent variable the national savings rate unlike previous studies, which generally referred to the household savings rate. National saving is important as it is a source of investment and one of the major determinants of macroeconomic growth. Also, as it is closely related to the demand for financial and real assets and it may affect asset price formation. In addition, we seek to avoid narrowing the aging impact as its takes into account companies and public sector saving (related to social sector, health, education and pensions). On another side, the household savings refers to survey measure which undervalues personal income as it provides information related to expenditure than to income sources. Likewise, it does not capture the same share of total saving for persons at different ages, so the estimate of relationship between savings and age may be fallacious.
As a definition, between the two known alternative measures of savings (S) we adopt that of national account (as income minus consumption expenditure) given data availability.5 Explicitly, we use the savings rate with respect to the gross national income disposable income6.
For independent variables, we refer to the main population aging indicators. We consider the mortality rate (MR) and fertility rate (FR) to capture demographic changes and its impact on the age structure composition, and likewise on the dependency ratio. We consider the old-age dependency ratio (EDR) to accurately look at the effect of aging besides the broadly used the total dependency ratio (TDR). Then, we could deduce if the aging impact is due to the fertility decline or to the longevity increase.
Concerning economic variables, we include three macroeconomic variables. (1) Basing to the neoclassical approach we introduce the interest rate (MMR) in particular the money market rate as a driver of the real interest rate (credit and debit). (2) As a one quantitative measure of aggregate income uncertainty we consider the aggregate unemployment rate (U). (3) In order to check the economic effect of saving, we examine the economic growth (G) measured by the GDP per capita at constant domestic prices. It is computed by dividing GDP per capita at current domestic prices by the consumption price index (base 1990). Hence, the inflation rate is indirectly considered.
The main statistical characteristics of these variables used are summarized in Table 1 (in the Appendix). Data are drawn from the Central Bank of Tunisia (CBT), the National Institution of Statistics (NIS) and Tunisian Institute of competitively and quantitative study (ITCQS).
Our analysis is based on the identification and estimation of structural vector autoregressive (SVAR). The SVAR model is used in macroeconomic analysis in order to check the effect of exogenous shocks (of the demographic change, for instance) on macroeconomic variables.
Our basic model VAR is the following:
where Yt is a column vector of stationary variables considered in the estimate.
The selection and order of independent variables are essential in the SVAR estimate. Thus, the independent demographic variables are introduced with caution following the demographic transition theory. As mortality decline brings that of fertility, so we first introduce the mortality rate (MR) followed by the fertility rate (FR). Then, we integrate the dependency ratio as an indicator of the population aging and the age structure change following the demographic transition.
After what, we consider the economic variable exogenous effect on saving. So, we insert the interest rate (MMR) as a saving determinant and the aggregate unemployment rate (U) as a measure of aggregate income uncertainty. Lastly, we introduce the national savings rate (S) followed by the economic growth (G) to check the aging impact on economic growth through the savings evolution.
As we use two dependency ratios, we estimate two distinct vectors autoregression. A vector includes the total dependency ratio which reflects the effect of both the mortality and fertility evolution as a result of the demographic policy as follows (MRt, FRt, TDRt, Ut, MMRt, St, Gt).
The second vector includes the old-age dependency ratio and takes the mortality choc as the main cause of the elderly proportion evolution as follows (MRt, EDRt, Ut, MMRt, St, Gt).
Otherwise, Γ(L) = Γ1L1 + Γ2L2 + … + Γp. Lp is a lag operator in the form of polynomial matrix and νt is a vector of idiosyncratic errors, where νt = (μ1t,…,μ5t)
where C(L) = [I - Γ(L)]−1.
The structural form (SF) of the model (1) can be written as follows:
where A(L) = C(L) H is the coefficient matrix (aij) of (7 × 7 or 6 × 6 for the two vectors respectively) size, and more precisely it represents the impulse response functions of the elements of Yt following the various shocks. Moreover, H is the transition matrix and ε is the vector of structural shocks where E (εtεt’) = IN.
However, the identification of these shocks requires the Cholesky decomposition in the order to identify the structure of the shocks. As a result, the decomposition of the variance covariance matrix of the reduced form residuals is written in a lower triangular matrix A(L). The number of constraints imposed on A(L) is equal to 21 i.e. n × (n-1) / 2 with n = 7 variables and where some of the structural shocks do not have contemporaneous impact on other variables.
Additionally, the Cholesky decomposition assumes that series listed earlier in the VAR order impact the others variables contemporaneously. But series listed later in the VAR order impact those listed earlier only with lag. Therefore, the variables listed early in the VAR order are considered more exogenous. As mentioned above, the order of endogenous variables is central to the identification of structural shocks, i.e. it determines the structure of the shocks. More precisely, the first variable has impacts on all the variables that are below it, but it does not receive any impacts from these variables. This rule applies to all subsequent variables. For instance, the triangular matrix A(L), for the case of n = 7 variables, is as follows.
Henceforth, we have to estimate four matrixes: a matrix (Alt1) for the total dependency ratio and one for the old-age dependency ratio (Alt2). Two others matrixes are also estimates as a robustness test by omitting the unemployment rate, respectively the matrixes (Alt3) and (Alt4).
To undertake the SVAR estimate model, we first study the stationarity of all variables using the Phillips-Perron test [26]. As reported in Table 2 (in the Appendix) all the considered variables are I(0) suggesting that a long-run (cointegration) relationship could exist between the considered variables.
Then we determine the order p of the VAR process to remember. To do this, we consider various processes for VAR lag orders p ranging from 1 to 4. For each model, we calculate the Akaike information criteria (AIC) and Schwarz (SC), and the log-likelihood (LV) to hold the p lag (=4) that minimizes these criteria as indicated in Table 3 (in the Appendix).
Accordingly, four alternatives are estimated, respectively with the identification of cointegration relationships by using the cointegration test of Johansen [27] as well as the structural factorization (with 500 iterations).
Finally, to examine the dynamic of the model, we refer to the impulse response function (IRF). It helps us to judge and to appreciate the channel(s) of population age structure change transmission. It allows to see if there is really a robust, stable and predictable relationship between aging and savings. In this respect, we will identify the different responses of all the variables in the model to various shocks. It should be noted that we focused on the effects of the shock on 10 periods and that errors are generated by Monte Carlo with 100 repetitions. Such analysis is strengthened with the variance decomposition analysis (VDC), which however, indicates the proportion of the variable changes due to own shocks versus shocks on the other variables. Namely, the variance of the forecast error of the change in savings rate is partitioned among the contributions of the innovations in each variable of the system.
Interestingly, results put forward that the LCH prediction is not automatically confirmed, but it is up to the economic uncertainty extent. Indeed, the LCH is not validated in the unemployment setting, which is considered in our study as an indirect measure of income uncertainty.
The SVAR’s estimate results (reported in Table 4 in the Appendix) points out that uncertainty encourages saving. Indeed, for the two aging indicators used (TDR and EDR) the LCH prediction is not validated once unemployment is introduced unlike Ahmedova’s [28] findings. As we note from matrixes Alt1 and Alt2, the two indicators present a significant positive effect on savings rate in the context of enduring unemployment without allowance, like in Frini’ work [29]. However, this effect is found more significant for old-age dependency ratio, unlike in Wong and Tang [30] and Loumrhari’s [31] findings.
In contrast, the LCH prediction is validated by the estimate omitting the unemployment rate, however, for only the total dependency ratio. Indeed, a significant negative effect is found in the matrix Alt3.
Such results confirm that the demographic changes impact on saving depends on the perception of the economic context and the confidence towards future. Furthermore, the LCH’s validation appears to be, as well, empirically related to the aging indicator used in the estimate. This confirms our proposal that the old-age dependency ratio indicator seems more efficient to explicitly check the effect of aging.
The unemployment which hints uncertainty about future income pushes the savers to keep up savings. It reduces confidence and intensifies incentives for precautionary saving so that, it prevents savings from decline. Indeed, the unemployment rate displays a significant and positive coefficient. The weight of the future uncertainty boosts the employed population to form a precautionary savings. This precautionary saving is important to offset the small amount of wealth accumulated after an enduring unemployment without any allocation benefit. When enduring a long unemployment period and facing great difficulties for credit liquidity at old age, elderly try to continue to save to keep up a certain level of consumption. Such behavior is very pronounced in Tunisia since retired do not benefit from a sufficient pension in a distressed pay-as-you-go system. The insufficiency of pension and medical care benefits entails the elderly saving’s behavior adjustment by continuing to work and to save at the beginning of the retirement period (as long as they remain in better health). As pointed out by Frini [32, 33] the new retirees or the youngest elderly (which share, generally, weighs more than that of the old retirees or the old elderly) maintain their savings mainly for precautionary motives in high uncertainty economic environment.
This Tunisian elderly saving behavior may in part be strengthened by the intentional transfers motivation of the old generation towards the young one. Indeed, Tunisian families, as stressed by Mahfoud [34] and Frini [35, 36], are strongly linked and directed by an intergenerational altruistic motive. So, the old generation do not seek to cut savings so as to help the young generation to face uncertain environment and hard economic conditions.
As expected, mortality drop induces a fertility decline, putting on show the demographic transition theory. This fertility decline increases the savings rate. It seems that the youth share decrease outweighs the small increase in the elderly share since the aggregate savings rate increases. Household with fewer children are likely to incur less expenditure in respect to their income for looking after them and then would save more. In addition, a reduced family size leads to a competition between children as a mean of transferring income from present to future and as a financial asset.7 Henceforth, by the fall of fertility rate, the demand of financial and capital market as a substitute of youth assurance service will increase and thus savings. Additionally, the decline of government expenditures for youth (given their share decline), seems to make up or even more the government expenditures increase for elderly (due to their share increase) to not lead savings decrease.
Considering uncertainty, mortality evolution positively influences savings rate when considering the economic and social facts, but negatively when they are neglected. The increase of mortality risk and health problem intensifies precautionary behavior to face health care expenditure at old age.
The uncertainty related to interest rate affects positively the savings rate. An increase in interest rate will make saving more attractive. Finally, like in AbuAl-Foul’s [37] work results show that no long-run relationship exists between saving and GDP growth. This in part due to that saving is, generally, done in real estate, which is known as a small creator of wealth with a small ripple effect.
Likewise, the IRF’s and VDC’s results underline that population aging on savings evolution changes respect to the economic uncertainty context. Savings positively respond to age structure changes once unemployment is taken into account. The different graphs of impulse responses (Figure 2 in the Appendix) show that savings respond quickly to demographic changes (mortality rate, fertility rate and dependency ratio jointly), but weakly to the shock of the money market rate. The response due to unemployment rate shock can be judged as significant with a return to equilibrium in the long-term. The saving response to economic growth innovations is, however, slow and limited. This analysis is corroborated out by the variance decomposition as displayed in Table 5 (in the Appendix).8 In detail, a relatively constant proportion of the change in savings rate variance is recorded for both ratios. The total dependency ratio shock is by about 3.75 percent for Alt1 and by 4.26 percent for Alt3 after three years. The old-age dependency ratio shocks are, however, of a less proportion by 1.42 percent for Alt2 and 0.16 percent for Alt4 over ten years. The noteworthy result is that savings evolution follow-up a shock of the total dependency ratio is more significant (by three times more) than of the elderly one. This fact is also proved by the dynamic response path. Fewer children lower the dependent population and consumption without contribution to income. The decrease of the youth dependent proportion out weights the increase of the elderly dependent in the proportion, which limits saving rate depression. This brings up the role of relative weight of the youth share to the elderly share on savings evolution. Further, the increase of elderly proportion appears not to cut savings rate. Thus, savings rises when fertility declines and longevity increases, but less intensively. In the contrary, to the LCH prediction, the old-age dependency ratio shock instantaneously and positively affects saving rate, however, more weakly than the total dependency ratio.
Remarkably, once we ignore the labour market unbalance (or uncertainty) of the estimates the relationship between aging and savings becomes consistent with the LCH prediction. The total dependency ratio shocks present a negative short-term impact on saving to disappear at long-run (after eight years). However, no impact is found for the old-age dependency ratio. This discrepancy in estimated magnitude through the two dependency ratios used refers back to our assumption that aging impact may be sensitive to the measurement used to describe it.
Moreover, demographic indicators shocks trace the variance of savings innovations. Mortality rate explains saving variance by almost the same small proportion (by about 2.30 percent) for all alternatives in the variance decomposition, but relatively less without the unemployment rate. In the impulse function graph, a negligible positive impact is found of mortality shock. Hence, with the rise of longevity and elderly proportion savings may not decline. Fertility decline significantly contributes in the savings change variance (by about 5.16 percent in Alt1) and even much more when forsaking the unemployment rate (by about 17.79 percent in Alt3). The corresponding impulse function displays a negative influence over six years to reverse positively after.
However, saving is less sensitive to interest rate shock. Money market rate contribution is more pronounced for the total dependency ratio than the elderly one. The same evidence is observed through the impulse function graph shown a very small positive influence which disappears in the long-term. This small impact of the real interest rate on saving may hide the offsetting of its two effects (of income and substitution). In other hand, it may be related to the Tunisian household’s behavior which seems to comply more with the Keynesian approach.
Finally, in the long-term, savings shocks seem to produce an effect on economic growth, but weakly when the imbalance labour market is considered (as reported in Table 6 in the Appendix). As mapped out by the response functions this dynamic is non-instantaneous. In contrast, a very small ‘feed-back’ seems to be produced of economic growth over three years on saving.
This study puts on show that the life cycle prediction of a downward pressure on saving by aging population could not be proved under uncertainty. Population aging is, on contrast, found to exert a long-term upward pressure on saving in an unemployment context. The economic environment’s uncertainty (such income uncertainty) quantified, in our case of study, by the unemployment phenomenon, looks to be an essential factor of the change in the life cycle pattern of savings. It is able to shaping the saving behavior and to distort the LCH. The impact of the demographic change seems strongly related to the economic confidence factors. Accordingly, the social and economic conditions limit the scope of the LCH. Thus, population aging will not necessarily spell disaster on national saving. Consequently, studies’ findings on developed countries could not be representative of saving behavioral in developing countries; where pension and medical insurance schemes are less developed and the persistent unemployment is without unemployment allowance benefit. Furthermore, it seems that the empirical findings checking the LCH depend on the aging indicator used. In fact, the use of the total dependency ratio could not validate the LCH, but it is validated by the old-age dependency ratio use. So, with more caution on the population aging measure, the evidence that elderly do not dissave may be found and the life cycle prediction may not be endorsed. Henceforth, the life cycle hypothesis may not be validated in macroeconomic approach as in the micro-econometric approach.
Finally, as policy implications, several measures are needed to sustain saving rate or to prevent it from an eventual decline. In addition to the strategy applied lately to postponing the retirement age to 62 years-old, Tunisian Policy-makers have to accelerate the move from the pay-as-you-ago public pension system towards the funded pension system to cut costs of increasing old-age benefits. As well, to mobilize more savings, they should shift the liquid savings towards long-term products. Accordingly, it is important to reconsider the long-term savings strategy to meet the household’s needs as well as the huge potential investment’s needs. Therefore, major economic and financial reforms should be undertaken to restructure public corporates and the partial openness of their capital, to strengthen the pension plans, to develop the insurance sector and promote life insurance, and to improve the framework of the stock market and the bond market and diversify product of savings.
Consumption,consumer income, wealth and saving over the life cycle.
S | MR | FR | EDR | TDR | G | U | TMM | |
---|---|---|---|---|---|---|---|---|
Mean | 20.73 | 0.68 | 3.55 | 14.21 | 75.70 | 4.52 | 15.28 | 6.85 |
Median | 21.75 | 0.59 | 3.01 | 14.35 | 77.05 | 4.67 | 15.60 | 6.40 |
Maximum | 26.40 | 1.34 | 6.29 | 20.08 | 108.69 | 17.74 | 18.30 | 11.79 |
Minimum | 9.40 | 0.55 | 2.00 | 11.15 | 50.51 | −1.92 | 12.40 | 3.00 |
Std. Dev. | 3.94 | 0.19 | 1.51 | 1.93 | 18.76 | 3.35 | 0.86 | 2.34 |
Observations | 50 | 50 | 50 | 50 | 50 | 50 | 50 | 50 |
Descriptive statistics variables.
Series | level | 1st difference |
---|---|---|
MR | 0.06* | 0.00* |
FR | 0.34 | 0.00* |
TDR | 0.80 | 0.00* |
EDR | 0.52 | 0.00* |
U | 0.01* | 0.00* |
TMM | 0.19 | 0.00* |
S | 0. 02* | 0.00** |
G | 0.04* | 0.00** |
Unit root test of ADF.
Note: The null hypothesis for the ADF test is that the series are non-stationary i.e. there is presence of unit root. The values in the table indicate the p-values of this test. Using the Phillips-Perron test, the results were the same.
* and **denotes that the null hypothesis of unit root is rejected at the 5% level and 10% level respectively.
The lag number p | AIC | SC | LV |
---|---|---|---|
Alternative 1 (MRt,FRt, TDRt, Ut, MMRt, St, Gt) | |||
1 | 4.56 | 5.62* | −36. 29 |
2 | 3.98 | 8.43 | 25.03 |
3 | 3.61 | 10.30 | 80.48 |
4 | −1.48* | 7.69 | 211.19* |
Alternative 2 (MRt, EDRt, Ut, TMMt, St, Gt) | |||
1 | 1.73 | 3.03* | 31.44 |
2 | 0.18 | 4.51 | 94.32 |
3 | −0.75 | 5.33 | 165.21 |
4 | −3.84* | 4.64 | 266.06* |
Alternative 3 (MRt,FRt, TDRt, TMMt, St, Gt) | |||
1 | 2.22 | 3.48* | 0.35 |
2 | 1.34 | 4.27 | 47.13 |
3 | 1.12 | 6.74 | 86.61 |
4 | −0.87* | 6.67 | 187.23* |
Alternative 4 (MRt, EDRt, TMMt, St, Gt) | |||
1 | 1.36 | 0.89* | 68.74 |
2 | −2.34 | 1.58 | 118.97 |
3 | −2.89 | 2.72 | 166.54 |
4 | −4.62* | 1.85 | 225.99* |
Choice of the lag number of VAR (p) process.
Note: LV denotes the log-likelihood; the asterisk indicates P order to retain according to the criterion used.
SVAR estimates results for the four alternatives.
Alt1 | ||||||||
---|---|---|---|---|---|---|---|---|
Period | S.E. | MR | D(FR) | D(TDR) | U | D(MMR) | S | G |
1 | 1.82 | 0.04 | 0.50 | 1.58 | 29.01 | 1.00 | 67.63 | 0.00 |
2 | 2.39 | 2.03 | 5.90 | 1.10 | 24.92 | 1.23 | 61.03 | 3.75 |
3 | 2.71 | 1.83 | 6.76 | 2.93 | 21.94 | 1.85 | 61.39 | 3.27 |
4 | 2.78 | 1.75 | 8.16 | 3.32 | 21.51 | 2.06 | 59.98 | 3.18 |
5 | 2.86 | 1.77 | 7.53 | 3.07 | 29.72 | 1.94 | 53.01 | 2.93 |
6 | 3.17 | 1.97 | 6.57 | 3.77 | 35.50 | 1.68 | 47.87 | 2.60 |
7 | 3.48 | 2.12 | 5.44 | 3.77 | 42.08 | 1.51 | 42.85 | 2.20 |
8 | 3.68 | 2.27 | 4.98 | 3.89 | 42.84 | 1.65 | 42.32 | 2.01 |
9 | 3.70 | 2.36 | 4.90 | 3.83 | 42.67 | 1.88 | 42.43 | 1.89 |
10 | 3.86 | 2.39 | 5.16 | 3.75 | 41.77 | 2.06 | 42.98 | 1.851 |
Alt2 | |||||||
---|---|---|---|---|---|---|---|
Period | S.E. | MR | D(EDR) | U | D(MMR) | S | G |
1 | 1.94 | 0.11 | 0.11 | 28.54 | 2.95 | 67.59 | 0.00 |
2 | 2.43 | 1.44 | 0.28 | 26.42 | 1.95 | 60.16 | 5.58 |
3 | 2.58 | 1.38 | 0.89 | 24.00 | 2.00 | 60.68 | 5.15 |
4 | 2.66 | 1.87 | 1.42 | 24.84 | 1.89 | 57.50 | 5.03 |
5 | 2.81 | 2.04 | 1.60 | 30.82 | 1.75 | 51.97 | 4.66 |
6 | 2.97 | 2.27 | 1.56 | 35.23 | 1.56 | 48.47 | 4.49 |
7 | 3.11 | 2.28 | 1.48 | 37.45 | 1.46 | 47.10 | 4.36 |
8 | 3.19 | 2.30 | 1.43 | 37.67 | 1.44 | 47.07 | 4.34 |
9 | 3.21 | 2.30 | 1.41 | 37.34 | 1.45 | 47.31 | 4.349 |
10 | 3.22 | 2.29 | 1.42 | 37.24 | 1.46 | 47.25 | 4.33 |
Alt3 | |||||||
---|---|---|---|---|---|---|---|
Period | S.E. | MR | D(FR) | D(TDR) | D(MMR) | S | G |
1 | 1.74 | 0.00 | 0.20 | 0.91 | 4.79 | 94.08 | 0.00 |
2 | 2.35 | 2.18 | 6.64 | 0.64 | 4.72 | 81.92 | 3.87 |
3 | 2.68 | 1.94 | 9.56 | 4.19 | 5.43 | 75.81 | 3.04 |
4 | 2.84 | 1.88 | 13.29 | 3.86 | 6.08 | 72.04 | 2.81 |
5 | 2.95 | 1.92 | 15.14 | 4.39 | 6.51 | 69.28 | 2.72 |
6 | 3.00 | 1.93 | 16.46 | 4.28 | 6.89 | 67.74 | 2.66 |
7 | 3.02 | 1.94 | 17.15 | 4.31 | 7.08 | 66.81 | 2.68 |
8 | 3.04 | 1.93 | 17.53 | 4.27 | 7.16 | 66.38 | 2.69 |
9 | 3.05 | 1.93 | 17.71 | 4.27 | 7.20 | 66.17 | 2.70 |
10 | 3.05 | 1.92 | 17.79 | 4.26 | 7.22 | 66.07 | 2.71 |
Alt4 | ||||||
---|---|---|---|---|---|---|
Period | S.E. | MR | D(EDR) | D(MMR) | S | G |
1 | 1.89 | 0.10 | 0.19 | 6.90 | 92.75 | 0.00 |
2 | 2.47 | 1.14 | 0.13 | 4.28 | 82.12 | 5.97 |
3 | 2.71 | 1.01 | 0.15 | 4.22 | 79.41 | 5.21 |
4 | 2.81 | 0.94 | 0.15 | 4.06 | 76.99 | 4.85 |
5 | 2.85 | 0.94 | 0.15 | 4.02 | 75.79 | 4.75 |
6 | 2.85 | 0.93 | 0.16 | 4.03 | 75.35 | 4.74 |
7 | 2.86 | 0.93 | 0.16 | 4.03 | 75.29 | 4.77 |
8 | 2.86 | 0.94 | 0.16 | 4.02 | 75.29 | 4.81 |
9 | 2.86 | 0.96 | 0.16 | 4.02 | 75.26 | 4.83 |
10 | 2.87 | 0.98 | 0.16 | 4.02 | 75.21 | 4.84 |
Variance decomposition of saving rates (Cholesky ordering).
Notes: Cholesky ordering follow that of the four alternatives. The second column (S.E) shows the forecast error of the variable at the given forecast horizon. The source of this forecast error is the variation in the current and future values of the innovations to each endogenous variable in the VAR. The other columns give the percentage of the forecast variance due to each innovation.
Alt1 | Alt2 | Alt3 | Alt4 |
---|---|---|---|
23.54 | 29.50 | 27.41 | 33.20 |
22.72 | 27.47 | 27.69 | 32.28 |
20.20 | 24.18 | 25.27 | 31.54 |
21.88 | 26.15 | 25.43 | 32.72 |
21.19 | 26.48 | 25.37 | 32.70 |
21.56 | 26.46 | 25.37 | 32.63 |
21.75 | 26.38 | 25.35 | 32.60 |
22.03 | 26.29 | 25.35 | 32.60 |
21.97 | 26.22 | 25.35 | 32.61 |
21.74 | 26.21 | 25.34 | 32. |
Variance decomposition of economic growth to saving rates.
Estimated impulse response functions. Response to Cholesky one S.D. innovations.
As an Open Access publisher, IntechOpen is dedicated to maintaining the highest ethical standards and principles in publishing. In addition, IntechOpen promotes the highest standards of integrity and ethical behavior in scientific research and peer-review. To maintain these principles IntechOpen has developed basic guidelines to facilitate the avoidance of Conflicts of Interest.
",metaTitle:"Conflicts of Interest Policy",metaDescription:"As an Open Access publisher, IntechOpen is dedicated to maintaining the highest ethical standards and principles in publishing. In addition, IntechOpen promotes the highest standards of integrity and ethical behavior in scientific research and peer-review.",metaKeywords:null,canonicalURL:"/page/conflicts-of-interest-policy",contentRaw:'[{"type":"htmlEditorComponent","content":"In each instance of a possible Conflict of Interest, IntechOpen aims to disclose the situation in as transparent a way as possible in order to allow readers to judge whether a particular potential Conflict of Interest has influenced the Work of any individual Author, Editor, or Reviewer. IntechOpen takes all possible Conflicts of Interest into account during the review process and ensures maximum transparency in implementing its policies.
\\n\\nA Conflict of Interest is a situation in which a person's professional judgment may be influenced by a range of factors, including financial gain, material interest, or some other personal or professional interest. For IntechOpen as a publisher, it is essential that all possible Conflicts of Interest are avoided. Each contributor, whether an Author, Editor, or Reviewer, who suspects they may have a Conflict of Interest, is obliged to declare that concern in order to make the publisher and the readership aware of any potential influence on the work being undertaken.
\\n\\nA Conflict of Interest can be identified at different phases of the publishing process.
\\n\\nIntechOpen requires:
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\\n\\nCONFLICT OF INTEREST – ACADEMIC EDITOR
\\n\\nEditors can also have Conflicts of Interest. Editors are expected to maintain the highest standards of conduct, which are outlined in our Best Practice Guidelines (templates for Best Practice Guidelines). Among other obligations, it is essential that Editors make transparent declarations of any possible Conflicts of Interest that they might have.
\\n\\nAvoidance Measures for Academic Editors of Conflicts of Interest:
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\\n\\nIf a manuscript is submitted by an Author who is a member of an Academic Editor's family or is personally or professionally related to the Academic Editor in any way, either as a friend, colleague, student or mentor, the work will be handled by a different Academic Editor who is not in any way connected to the Author.
\\n\\nCONFLICT OF INTEREST - REVIEWER
\\n\\nAll Reviewers are required to declare possible Conflicts of Interest at the beginning of the evaluation process. If a Reviewer feels he or she might have any material, financial or any other conflict of interest with regards to the manuscript being reviewed, he or she is required to declare such concern and, if necessary, request exclusion from any further involvement in the evaluation process. A Reviewer's potential Conflicts of Interest are declared in the review report and presented to the Academic Editor, who then assesses whether or not the declared potential or actual Conflicts of Interest had, or could be perceived to have had, any significant impact on the review itself.
\\n\\nEXAMPLES OF CONFLICTS OF INTEREST:
\\n\\nFINANCIAL AND MATERIAL
\\n\\nNON-FINANCIAL
\\n\\nAuthors are required to declare all potentially relevant non-financial, financial and material Conflicts of Interest that may have had an influence on their scientific work.
\\n\\nAcademic Editors and Reviewers are required to declare any non-financial, financial and material Conflicts of Interest that could influence their fair and balanced evaluation of manuscripts. If such conflict exists with regards to a submitted manuscript, Academic Editors and Reviewers should exclude themselves from handling it.
\\n\\nAll Authors, Academic Editors, and Reviewers are required to declare all possible financial and material Conflicts of Interest in the last five years, although it is advisable to declare less recent Conflicts of Interest as well.
\\n\\nEXAMPLES:
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\\n\\nAuthors should declare if they are board members of an organization that could benefit financially or materially from the publication of their work.
\\n\\nAcademic Editors should declare if they were coauthors or they have worked on the research project with the Author who has submitted a manuscript.
\\n\\nAcademic Editors should declare if the Author of a submitted manuscript is affiliated with the same department, faculty, institute, or company as they are.
\\n\\nPolicy last updated: 2016-06-09
\\n"}]'},components:[{type:"htmlEditorComponent",content:"In each instance of a possible Conflict of Interest, IntechOpen aims to disclose the situation in as transparent a way as possible in order to allow readers to judge whether a particular potential Conflict of Interest has influenced the Work of any individual Author, Editor, or Reviewer. IntechOpen takes all possible Conflicts of Interest into account during the review process and ensures maximum transparency in implementing its policies.
\n\nA Conflict of Interest is a situation in which a person's professional judgment may be influenced by a range of factors, including financial gain, material interest, or some other personal or professional interest. For IntechOpen as a publisher, it is essential that all possible Conflicts of Interest are avoided. Each contributor, whether an Author, Editor, or Reviewer, who suspects they may have a Conflict of Interest, is obliged to declare that concern in order to make the publisher and the readership aware of any potential influence on the work being undertaken.
\n\nA Conflict of Interest can be identified at different phases of the publishing process.
\n\nIntechOpen requires:
\n\nCONFLICT OF INTEREST - AUTHOR
\n\nAll Authors are obliged to declare every existing or potential Conflict of Interest, including financial or personal factors, as well as any relationship which could influence their scientific work. Authors must declare Conflicts of Interest at the time of manuscript submission, although they may exceptionally do so at any point during manuscript review. For jointly prepared manuscripts, the corresponding Author is obliged to declare potential Conflicts of Interest of any other Authors who have contributed to the manuscript.
\n\nCONFLICT OF INTEREST – ACADEMIC EDITOR
\n\nEditors can also have Conflicts of Interest. Editors are expected to maintain the highest standards of conduct, which are outlined in our Best Practice Guidelines (templates for Best Practice Guidelines). Among other obligations, it is essential that Editors make transparent declarations of any possible Conflicts of Interest that they might have.
\n\nAvoidance Measures for Academic Editors of Conflicts of Interest:
\n\nFor manuscripts submitted by the Academic Editor (or a scientific advisor), an appropriate person will be appointed to handle and evaluate the manuscript. The appointed handling Editor's identity will not be disclosed to the Author in order to maintain impartiality and anonymity of the review.
\n\nIf a manuscript is submitted by an Author who is a member of an Academic Editor's family or is personally or professionally related to the Academic Editor in any way, either as a friend, colleague, student or mentor, the work will be handled by a different Academic Editor who is not in any way connected to the Author.
\n\nCONFLICT OF INTEREST - REVIEWER
\n\nAll Reviewers are required to declare possible Conflicts of Interest at the beginning of the evaluation process. If a Reviewer feels he or she might have any material, financial or any other conflict of interest with regards to the manuscript being reviewed, he or she is required to declare such concern and, if necessary, request exclusion from any further involvement in the evaluation process. A Reviewer's potential Conflicts of Interest are declared in the review report and presented to the Academic Editor, who then assesses whether or not the declared potential or actual Conflicts of Interest had, or could be perceived to have had, any significant impact on the review itself.
\n\nEXAMPLES OF CONFLICTS OF INTEREST:
\n\nFINANCIAL AND MATERIAL
\n\nNON-FINANCIAL
\n\nAuthors are required to declare all potentially relevant non-financial, financial and material Conflicts of Interest that may have had an influence on their scientific work.
\n\nAcademic Editors and Reviewers are required to declare any non-financial, financial and material Conflicts of Interest that could influence their fair and balanced evaluation of manuscripts. If such conflict exists with regards to a submitted manuscript, Academic Editors and Reviewers should exclude themselves from handling it.
\n\nAll Authors, Academic Editors, and Reviewers are required to declare all possible financial and material Conflicts of Interest in the last five years, although it is advisable to declare less recent Conflicts of Interest as well.
\n\nEXAMPLES:
\n\nAuthors should declare if they were or they still are Academic Editors of the publications in which they wish to publish their work.
\n\nAuthors should declare if they are board members of an organization that could benefit financially or materially from the publication of their work.
\n\nAcademic Editors should declare if they were coauthors or they have worked on the research project with the Author who has submitted a manuscript.
\n\nAcademic Editors should declare if the Author of a submitted manuscript is affiliated with the same department, faculty, institute, or company as they are.
\n\nPolicy last updated: 2016-06-09
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Osseointegration",slug:"dental-implant-surface-enhancement-and-osseointegration",totalDownloads:18676,totalCrossrefCites:38,totalDimensionsCites:99,abstract:null,book:{id:"179",slug:"implant-dentistry-a-rapidly-evolving-practice",title:"Implant Dentistry",fullTitle:"Implant Dentistry - A Rapidly Evolving Practice"},signatures:"S.Anil, P.S. Anand, H. Alghamdi and J.A. Jansen",authors:[{id:"25232",title:"Prof.",name:"Sukumaran",middleName:null,surname:"Anil",slug:"sukumaran-anil",fullName:"Sukumaran Anil"},{id:"28373",title:"Prof.",name:"John",middleName:null,surname:"Jansen",slug:"john-jansen",fullName:"John Jansen"},{id:"77058",title:"Dr.",name:"Seham",middleName:null,surname:"Alyafei",slug:"seham-alyafei",fullName:"Seham Alyafei"},{id:"82073",title:"Dr.",name:"Subhash",middleName:null,surname:"Narayanan",slug:"subhash-narayanan",fullName:"Subhash Narayanan"}]},{id:"18415",doi:"10.5772/16936",title:"Osseointegration and Bioscience of Implant Surfaces - Current Concepts at Bone-Implant Interface",slug:"osseointegration-and-bioscience-of-implant-surfaces-current-concepts-at-bone-implant-interface",totalDownloads:12502,totalCrossrefCites:16,totalDimensionsCites:42,abstract:null,book:{id:"179",slug:"implant-dentistry-a-rapidly-evolving-practice",title:"Implant Dentistry",fullTitle:"Implant Dentistry - A Rapidly Evolving Practice"},signatures:"Mustafa Ramazanoglu and Yoshiki Oshida",authors:[{id:"26726",title:"Prof.",name:"Yoshiki",middleName:null,surname:"Oshida",slug:"yoshiki-oshida",fullName:"Yoshiki Oshida"},{id:"29841",title:"Prof.",name:"Mustafa",middleName:null,surname:"Ramazanoglu",slug:"mustafa-ramazanoglu",fullName:"Mustafa Ramazanoglu"}]},{id:"18426",doi:"10.5772/18746",title:"Factors Affecting the Success of Dental Implants",slug:"factors-affecting-the-success-of-dental-implants",totalDownloads:17474,totalCrossrefCites:9,totalDimensionsCites:35,abstract:null,book:{id:"179",slug:"implant-dentistry-a-rapidly-evolving-practice",title:"Implant Dentistry",fullTitle:"Implant Dentistry - A Rapidly Evolving Practice"},signatures:"Carlos Nelson Elias",authors:[{id:"32438",title:"Prof.",name:"Carlos",middleName:null,surname:"Elias",slug:"carlos-elias",fullName:"Carlos Elias"}]},{id:"18414",doi:"10.5772/17512",title:"Dental Implant Surfaces – Physicochemical Properties, Biological Performance, and Trends",slug:"dental-implant-surfaces-physicochemical-properties-biological-performance-and-trends",totalDownloads:13080,totalCrossrefCites:5,totalDimensionsCites:30,abstract:null,book:{id:"179",slug:"implant-dentistry-a-rapidly-evolving-practice",title:"Implant Dentistry",fullTitle:"Implant Dentistry - A Rapidly Evolving Practice"},signatures:"Ahmed M. Ballo, Omar Omar, Wei Xia and Anders Palmquist",authors:[{id:"19042",title:"Dr.",name:"Wei",middleName:null,surname:"Xia",slug:"wei-xia",fullName:"Wei Xia"},{id:"28549",title:"Dr.",name:"Ahmed",middleName:"M.",surname:"Ballo",slug:"ahmed-ballo",fullName:"Ahmed Ballo"},{id:"81291",title:"Dr.",name:"Omar",middleName:null,surname:"Omar",slug:"omar-omar",fullName:"Omar Omar"},{id:"81292",title:"Dr.",name:"Anders",middleName:null,surname:"Palmquist",slug:"anders-palmquist",fullName:"Anders Palmquist"}]},{id:"18417",doi:"10.5772/18309",title:"Implant Stability - Measuring Devices and Randomized Clinical Trial for ISQ Value Change Pattern Measured from Two Different Directions by Magnetic RFA",slug:"implant-stability-measuring-devices-and-randomized-clinical-trial-for-isq-value-change-pattern-measu",totalDownloads:13176,totalCrossrefCites:8,totalDimensionsCites:19,abstract:null,book:{id:"179",slug:"implant-dentistry-a-rapidly-evolving-practice",title:"Implant Dentistry",fullTitle:"Implant Dentistry - A Rapidly Evolving Practice"},signatures:"Jong-Chul Park, Jung-Woo Lee, Soung-Min Kim and Jong-Ho Lee",authors:[{id:"31057",title:"Prof.",name:"Jong-Ho",middleName:null,surname:"Lee",slug:"jong-ho-lee",fullName:"Jong-Ho Lee"},{id:"48351",title:"Prof.",name:"Jong-Chul",middleName:null,surname:"Park",slug:"jong-chul-park",fullName:"Jong-Chul Park"},{id:"83313",title:"Dr.",name:"JungWoo",middleName:null,surname:"Lee",slug:"jungwoo-lee",fullName:"JungWoo Lee"}]}],mostDownloadedChaptersLast30Days:[{id:"18432",title:"Clinical Complications of Dental Implants",slug:"clinical-complications-of-dental-implants",totalDownloads:56478,totalCrossrefCites:2,totalDimensionsCites:5,abstract:null,book:{id:"179",slug:"implant-dentistry-a-rapidly-evolving-practice",title:"Implant Dentistry",fullTitle:"Implant Dentistry - A Rapidly Evolving Practice"},signatures:"Su-Gwan Kim",authors:[{id:"27797",title:"Prof.",name:"Su-Gwan",middleName:null,surname:"Kim",slug:"su-gwan-kim",fullName:"Su-Gwan Kim"}]},{id:"47927",title:"Miniscrew Applications in Orthodontics",slug:"miniscrew-applications-in-orthodontics",totalDownloads:4697,totalCrossrefCites:0,totalDimensionsCites:2,abstract:null,book:{id:"4548",slug:"current-concepts-in-dental-implantology",title:"Current Concepts in Dental Implantology",fullTitle:"Current Concepts in Dental Implantology"},signatures:"Fatma Deniz Uzuner and Belma Işık Aslan",authors:[{id:"42847",title:"Dr.",name:"Belma",middleName:null,surname:"Işik Aslan",slug:"belma-isik-aslan",fullName:"Belma Işik Aslan"},{id:"172009",title:"Dr.",name:"Fatma Deniz",middleName:null,surname:"Uzuner",slug:"fatma-deniz-uzuner",fullName:"Fatma Deniz Uzuner"}]},{id:"50308",title:"Antibiotics in Implant Dentistry",slug:"antibiotics-in-implant-dentistry",totalDownloads:2369,totalCrossrefCites:1,totalDimensionsCites:1,abstract:"Antibiotics have been recommended either as an extended treatment for several days or as a single antibiotic prophylaxis dose since the development of dental implant osseointegration technique in the 1970s. It is also performed as part of surgical protocol during the peri-operative phase in the treatment of peri-implantitis. To date, there is a lack of scientific evidence regarding the additive effect of antibiotics in the treatment of dental implant. This has thus left the clinician with inconclusive recommendations, leading to increase antibiotic prescription. With this increase, the development of antibiotic resistance is becoming a threat to modern healthcare that requires revisiting of current indications and implementation of rational treatment strategies. Therefore, more studies are needed to assess the benefit of antibiotic prescription and whether it is safe to refrain from its use.",book:{id:"5185",slug:"dental-implantology-and-biomaterial",title:"Dental Implantology and Biomaterial",fullTitle:"Dental Implantology and Biomaterial"},signatures:"Dalia Khalil, Bodil Lund and Margareta Hultin",authors:[{id:"179031",title:"Dr.",name:"Dalia",middleName:null,surname:"Khalil",slug:"dalia-khalil",fullName:"Dalia Khalil"},{id:"185113",title:"Dr.",name:"Bodil",middleName:null,surname:"Lund",slug:"bodil-lund",fullName:"Bodil Lund"},{id:"185114",title:"Dr.",name:"Margareta",middleName:null,surname:"Hultin",slug:"margareta-hultin",fullName:"Margareta Hultin"}]},{id:"47915",title:"Rationale for Dental Implants",slug:"rationale-for-dental-implants",totalDownloads:3076,totalCrossrefCites:0,totalDimensionsCites:2,abstract:null,book:{id:"4548",slug:"current-concepts-in-dental-implantology",title:"Current Concepts in Dental Implantology",fullTitle:"Current Concepts in Dental Implantology"},signatures:"Ilser Turkyilmaz and Gokce Soganci",authors:[{id:"171984",title:"Associate Prof.",name:"Ilser",middleName:null,surname:"Turkyilmaz",slug:"ilser-turkyilmaz",fullName:"Ilser Turkyilmaz"}]},{id:"18430",title:"An Important Dilemma in Treatment Planning: Implant or Endodontic Therapy?",slug:"an-important-dilemma-in-treatment-planning-implant-or-endodontic-therapy-",totalDownloads:6264,totalCrossrefCites:0,totalDimensionsCites:0,abstract:null,book:{id:"179",slug:"implant-dentistry-a-rapidly-evolving-practice",title:"Implant Dentistry",fullTitle:"Implant Dentistry - A Rapidly Evolving Practice"},signatures:"Funda Kont Cobankara and Sema Belli",authors:[{id:"28846",title:"Dr.",name:"Funda",middleName:null,surname:"Kont Çobankara",slug:"funda-kont-cobankara",fullName:"Funda Kont Çobankara"},{id:"75862",title:"Prof.",name:"Sema",middleName:null,surname:"Belli",slug:"sema-belli",fullName:"Sema Belli"}]}],onlineFirstChaptersFilter:{topicId:"998",limit:6,offset:0},onlineFirstChaptersCollection:[{id:"81595",title:"Prosthetic Concepts in Dental Implantology",slug:"prosthetic-concepts-in-dental-implantology",totalDownloads:25,totalDimensionsCites:0,doi:"10.5772/intechopen.104725",abstract:"This chapter will address evidence-based prosthetic concepts in dental implantology as well as clinical evidence with focus on appropriate logic and technical skills. Those prosthetic factors are as just important as surgical factors, and long-term success can only be achieved if both of those factors are considered, respected, and strictly followed from planning to prosthetic phase of treatment. This chapter will deal with materials selection for prosthetic part, shape, size, and design of supracrestal parts of abutments and their influence on soft tissue and bone stability around dental implants. Furthermore, one of most important decisions is about choosing the proper way of retention: screw- vs. cement-retained restorations, and it will be discussed in detail. Additionally, emergence profile and its function in soft tissues adaptation and adhesion to different prosthetic materials also have important role in long-term success of dental implant restorations.",book:{id:"10808",title:"Current Concepts in Dental Implantology - From Science to Clinical Research",coverURL:"https://cdn.intechopen.com/books/images_new/10808.jpg"},signatures:"Ivica Pelivan"},{id:"80500",title:"Novel Dental Implants with Herbal Composites: A Review",slug:"novel-dental-implants-with-herbal-composites-a-review",totalDownloads:49,totalDimensionsCites:0,doi:"10.5772/intechopen.101489",abstract:"Missing a permanent tooth is a miserable condition faced by a common man. A tooth decay, periodontitis, mechanical trauma, or any systemic complications lead to such a complication. These bone defects when left untreated lead to severe resorption of the alveolar bone. A proper dental filling with an appropriate bone substitute material could prevent such resorption and paves a way for subsequent implant placement. Dental implants are considered as the prime option by dentists to replace a single tooth or prevent bone resorption. A variety of bone substitutes are available differ in origin, consistency, particle size, porosity, and resorption characteristics. Herbal composites in dentistry fabricated using biphospho-calcium phosphate, casein, chitosan, and certain herbal extracts of Cassia occidentalis, Terminalia arjuna bark, Myristica fragans also were reported to possess a higher ossification property, osteogenic property and were able to repair bone defects. C. occidentalis was reported to stimulate mineralization of the bone and osteoblastic differentiation through the activation of the PI3K-Akt/MAPKs pathway in MC3T3-E1 cells of mice. This implant proved better osteoconductivity and bioactivity compared to pure HAP and other BCP ratios. Terminalia Arjuna was also worked in the incorporation in the graft to enhance the osteogenic property of the implant and gave good results. Another implant bone graft was synthesized containing BCP, biocompatible casein, and the extracts of Myristica fragans and subjected to in vitro investigations and the results revealed the deposition of apatite on the graft after immersing in SBF and also the ALP activity was high when treated with MG-63 cells, NIH-3 T3, and Saos 2 cell lines. This study indicates that the inclusion of plant extract enhances the osteogenic property of the graft. Thus, these novel dental implants incorporated with herbal composites evaluated by researchers revealed an enhanced bone healing, accelerates osseointegration, inhibits osteopenia, and inhibits inflammation. This application of herbal composite inclusion in dentistry and its applications has a greater potential to improve the success rate of dental implants and allows the implications of biotechnology in implant dentistry.",book:{id:"10808",title:"Current Concepts in Dental Implantology - From Science to Clinical Research",coverURL:"https://cdn.intechopen.com/books/images_new/10808.jpg"},signatures:"Gopathy Sridevi and Seshadri Srividya"},{id:"78320",title:"Implant-Retained Maxillary and Mandibular Overdentures - A Solution for Completely Edentulous Patients",slug:"implant-retained-maxillary-and-mandibular-overdentures-a-solution-for-completely-edentulous-patients",totalDownloads:66,totalDimensionsCites:0,doi:"10.5772/intechopen.99575",abstract:"The main goal of modern removable prosthodontics is to restore the normal appearance, function, esthetics and speech in each completely edentulous patient. However, if all teeth are missing in a patient, it becomes very complicated to achieve it using traditional protocols. Therefore, implants were introduced into removable prosthodontics to ensure better retention and stability of the conventional dentures. In case of a large amount of bone missing in the jaw it is necessary to ensure the functioning of the dentures constructing various additional stabilizing and retentive prosthodontic solutions on the osseointegrated implants. Numerous types of attachment systems have been used recently for relating implant-retained overdentures to underlying implants: basically splinting (various bar shape designs) and non-splinting attachments (various ball type attachment, magnet attachment, telescopic coping systems). Indications for their use depend on the surgical and prosthodontic factors such as the number and position of the implants, the amount of free intermaxillary space and the type and size of the overdentures. Different indications, types of the overdentures and the attachment systems will be discussed in this chapter.",book:{id:"10808",title:"Current Concepts in Dental Implantology - From Science to Clinical Research",coverURL:"https://cdn.intechopen.com/books/images_new/10808.jpg"},signatures:"Dubravka Knezović Zlatarić, Robert Ćelić and Hrvoje Pezo"},{id:"79724",title:"Implant Stability Quotient (ISQ): A Reliable Guide for Implant Treatment",slug:"implant-stability-quotient-isq-a-reliable-guide-for-implant-treatment",totalDownloads:60,totalDimensionsCites:0,doi:"10.5772/intechopen.101359",abstract:"Implant stability is a prerequisite for successful dental implants and osseointegration. To determine the status of implant stability, continuous monitoring in an objective and qualitative manner is important. To measure implant stability two different stages are there: Primary and secondary. Primary implant stability at placement is a mechanical phenomenon that is related to the local bone quality and quantity, the type of implant and placement technique used. Primary stability is checked from mechanical engagement with cortical bone. Secondary stability is developed from regeneration and remodeling of the bone and tissue around the implant after insertion and affected by the primary stability, bone formation and remodeling. Implant stability is essential for the time of functional loading. Classical benchmark methods to measure implant stability were radiographs or microscopic analysis, removal torque, push-through and pull-through but due to lack of feasibility, time consumption and ethical reasons other methods have been propounded over period of time like measurement of implant torque, model analysis and most important ISQ which has the ability to monitor osseointegration and the life expectancy of an implant. ISQ is a valuable diagnostic and clinical tool that has far-reaching consequences on implant dentistry and this article throws light on advanced and reliable methods of assessing ISQ.",book:{id:"10808",title:"Current Concepts in Dental Implantology - From Science to Clinical Research",coverURL:"https://cdn.intechopen.com/books/images_new/10808.jpg"},signatures:"Gaurav Gupta"},{id:"79817",title:"Peri-Implant Soft Tissue Augmentation",slug:"peri-implant-soft-tissue-augmentation",totalDownloads:128,totalDimensionsCites:0,doi:"10.5772/intechopen.101336",abstract:"The peri-implant soft tissue (PIS) augmentation procedure has become an integral part of implant-prosthetic rehabilitation. Minimal width of keratinized mucosa (KM) of 2 mm is deemed necessary to facilitate oral hygiene maintenance around the implant and provide hard and soft peri-implant tissue stability. PIS thickness of at least 2 mm is recommended to achieve the esthetic appearance and prevent recessions around implant prosthetic rehabilitation. The autogenous soft tissue grafts can be divided into two groups based on their histological composition—free gingival graft (FGG) and connective tissue graft (CTG). FGG graft is used mainly to increase the width of keratinized mucosa while CTG augment the thickness of PIS. Both grafts are harvested from the same anatomical region—the palate. Alternatively, they can be harvested from the maxillary tuberosity. Soft tissue grafts can be also harvested as pedicle grafts, in case when the soft tissue graft remains attached to the donor site by one side preserving the blood supply from the donor region. Clinically this will result in less shrinkage of the graft postoperatively, improving the outcome of the augmentation procedure. To bypass the drawback connected with FGG or CTG harvesting, substitutional soft tissue grafts have been developed.",book:{id:"10808",title:"Current Concepts in Dental Implantology - From Science to Clinical Research",coverURL:"https://cdn.intechopen.com/books/images_new/10808.jpg"},signatures:"Marko Blašković and Dorotea Blašković"},{id:"79611",title:"Growth Factors and Dental Implantology",slug:"growth-factors-and-dental-implantology",totalDownloads:103,totalDimensionsCites:0,doi:"10.5772/intechopen.101082",abstract:"Normal healing procedure of bone involves various sequential events to develop bone and bridge the bone -to- bone gap. When this healing occurs with a metal (titanium) fixture on one side, it is called as osseointegration. After extensive studies on this topic, it is found that this procedure occurs in presence of various biologic constituents that are spontaneously released at the site. Thus, to accelerate normal healing after implant placement and make results more predictable, it has been proposed to use these autologous factors in the osteotomy site. Since it is the beginning of a new revolution in dental implantology, right now it is essential to analyze all possible combinations of host conditions, bone quality and quantity and bio factors being used. This can definitely be a boon for the patients with compromised systemic or local conditions.",book:{id:"10808",title:"Current Concepts in Dental Implantology - From Science to Clinical Research",coverURL:"https://cdn.intechopen.com/books/images_new/10808.jpg"},signatures:"Deeksha Gupta"}],onlineFirstChaptersTotal:17},preDownload:{success:null,errors:{}},subscriptionForm:{success:null,errors:{}},aboutIntechopen:{},privacyPolicy:{},peerReviewing:{},howOpenAccessPublishingWithIntechopenWorks:{},sponsorshipBooks:{sponsorshipBooks:[],offset:8,limit:8,total:0},allSeries:{pteSeriesList:[{id:"14",title:"Artificial Intelligence",numberOfPublishedBooks:9,numberOfPublishedChapters:89,numberOfOpenTopics:6,numberOfUpcomingTopics:0,issn:"2633-1403",doi:"10.5772/intechopen.79920",isOpenForSubmission:!0},{id:"7",title:"Biomedical Engineering",numberOfPublishedBooks:12,numberOfPublishedChapters:104,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2631-5343",doi:"10.5772/intechopen.71985",isOpenForSubmission:!0}],lsSeriesList:[{id:"11",title:"Biochemistry",numberOfPublishedBooks:32,numberOfPublishedChapters:318,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2632-0983",doi:"10.5772/intechopen.72877",isOpenForSubmission:!0},{id:"25",title:"Environmental Sciences",numberOfPublishedBooks:1,numberOfPublishedChapters:12,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2754-6713",doi:"10.5772/intechopen.100362",isOpenForSubmission:!0},{id:"10",title:"Physiology",numberOfPublishedBooks:11,numberOfPublishedChapters:141,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-8261",doi:"10.5772/intechopen.72796",isOpenForSubmission:!0}],hsSeriesList:[{id:"3",title:"Dentistry",numberOfPublishedBooks:8,numberOfPublishedChapters:129,numberOfOpenTopics:2,numberOfUpcomingTopics:0,issn:"2631-6218",doi:"10.5772/intechopen.71199",isOpenForSubmission:!0},{id:"6",title:"Infectious Diseases",numberOfPublishedBooks:13,numberOfPublishedChapters:113,numberOfOpenTopics:3,numberOfUpcomingTopics:1,issn:"2631-6188",doi:"10.5772/intechopen.71852",isOpenForSubmission:!0},{id:"13",title:"Veterinary Medicine and Science",numberOfPublishedBooks:11,numberOfPublishedChapters:106,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2632-0517",doi:"10.5772/intechopen.73681",isOpenForSubmission:!0}],sshSeriesList:[{id:"22",title:"Business, Management and Economics",numberOfPublishedBooks:1,numberOfPublishedChapters:19,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2753-894X",doi:"10.5772/intechopen.100359",isOpenForSubmission:!0},{id:"23",title:"Education and Human Development",numberOfPublishedBooks:0,numberOfPublishedChapters:5,numberOfOpenTopics:1,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100360",isOpenForSubmission:!0},{id:"24",title:"Sustainable Development",numberOfPublishedBooks:0,numberOfPublishedChapters:15,numberOfOpenTopics:5,numberOfUpcomingTopics:0,issn:null,doi:"10.5772/intechopen.100361",isOpenForSubmission:!0}],testimonialsList:[{id:"6",text:"It is great to work with the IntechOpen to produce a worthwhile collection of research that also becomes a great educational resource and guide for future research endeavors.",author:{id:"259298",name:"Edward",surname:"Narayan",institutionString:null,profilePictureURL:"https://mts.intechopen.com/storage/users/259298/images/system/259298.jpeg",slug:"edward-narayan",institution:{id:"3",name:"University of Queensland",country:{id:null,name:"Australia"}}}},{id:"13",text:"The collaboration with and support of the technical staff of IntechOpen is fantastic. 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Much of biochemistry is devoted to enzymes, proteins that catalyze chemical reactions, enzyme structures, mechanisms of action and their roles within cells. Biochemistry also studies small signaling molecules, coenzymes, inhibitors, vitamins, and hormones, which play roles in life processes. Biochemical experimentation, besides coopting classical chemistry methods, e.g., chromatography, adopted new techniques, e.g., X-ray diffraction, electron microscopy, NMR, radioisotopes, and developed sophisticated microbial genetic tools, e.g., auxotroph mutants and their revertants, fermentation, etc. More recently, biochemistry embraced the ‘big data’ omics systems. Initial biochemical studies have been exclusively analytic: dissecting, purifying, and examining individual components of a biological system; in the apt words of Efraim Racker (1913 –1991), “Don’t waste clean thinking on dirty enzymes.” Today, however, biochemistry is becoming more agglomerative and comprehensive, setting out to integrate and describe entirely particular biological systems. The ‘big data’ metabolomics can define the complement of small molecules, e.g., in a soil or biofilm sample; proteomics can distinguish all the comprising proteins, e.g., serum; metagenomics can identify all the genes in a complex environment, e.g., the bovine rumen. This Biochemistry Series will address the current research on biomolecules and the emerging trends with great promise.",coverUrl:"https://cdn.intechopen.com/series/covers/11.jpg",latestPublicationDate:"June 29th, 2022",hasOnlineFirst:!0,numberOfPublishedBooks:32,editor:{id:"31610",title:"Dr.",name:"Miroslav",middleName:null,surname:"Blumenberg",slug:"miroslav-blumenberg",fullName:"Miroslav Blumenberg",profilePictureURL:"https://mts.intechopen.com/storage/users/31610/images/system/31610.jpg",biography:"Miroslav Blumenberg, Ph.D., was born in Subotica and received his BSc in Belgrade, Yugoslavia. He completed his Ph.D. at MIT in Organic Chemistry; he followed up his Ph.D. with two postdoctoral study periods at Stanford University. Since 1983, he has been a faculty member of the RO Perelman Department of Dermatology, NYU School of Medicine, where he is codirector of a training grant in cutaneous biology. Dr. Blumenberg’s research is focused on the epidermis, expression of keratin genes, transcription profiling, keratinocyte differentiation, inflammatory diseases and cancers, and most recently the effects of the microbiome on the skin. He has published more than 100 peer-reviewed research articles and graduated numerous Ph.D. and postdoctoral students.",institutionString:null,institution:{name:"New York University Langone Medical Center",institutionURL:null,country:{name:"United States of America"}}},editorTwo:null,editorThree:null},subseries:{paginationCount:4,paginationItems:[{id:"14",title:"Cell and Molecular Biology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/14.jpg",isOpenForSubmission:!0,editor:{id:"165627",title:"Dr.",name:"Rosa María",middleName:null,surname:"Martínez-Espinosa",slug:"rosa-maria-martinez-espinosa",fullName:"Rosa María Martínez-Espinosa",profilePictureURL:"https://mts.intechopen.com/storage/users/165627/images/system/165627.jpeg",biography:"Dr. Rosa María Martínez-Espinosa has been a Spanish Full Professor since 2020 (Biochemistry and Molecular Biology) and is currently Vice-President of International Relations and Cooperation development and leader of the research group 'Applied Biochemistry” (University of Alicante, Spain). Other positions she has held at the university include Vice-Dean of Master Programs, Vice-Dean of the Degree in Biology and Vice-Dean for Mobility and Enterprise and Engagement at the Faculty of Science (University of Alicante). She received her Bachelor in Biology in 1998 (University of Alicante) and her PhD in 2003 (Biochemistry, University of Alicante). She undertook post-doctoral research at the University of East Anglia (Norwich, U.K. 2004-2005; 2007-2008).\nHer multidisciplinary research focuses on investigating archaea and their potential applications in biotechnology. She has an H-index of 21. She has authored one patent and has published more than 70 indexed papers and around 60 book chapters.\nShe has contributed to more than 150 national and international meetings during the last 15 years. Her research interests include archaea metabolism, enzymes purification and characterization, gene regulation, carotenoids and bioplastics production, antioxidant\ncompounds, waste water treatments, and brines bioremediation.\nRosa María’s other roles include editorial board member for several journals related\nto biochemistry, reviewer for more than 60 journals (biochemistry, molecular biology, biotechnology, chemistry and microbiology) and president of several organizing committees in international meetings related to the N-cycle or respiratory processes.",institutionString:null,institution:{name:"University of Alicante",institutionURL:null,country:{name:"Spain"}}},editorTwo:null,editorThree:null},{id:"15",title:"Chemical Biology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/15.jpg",isOpenForSubmission:!0,editor:{id:"441442",title:"Dr.",name:"Şükrü",middleName:null,surname:"Beydemir",slug:"sukru-beydemir",fullName:"Şükrü Beydemir",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00003GsUoIQAV/Profile_Picture_1634557147521",biography:"Dr. Şükrü Beydemir obtained a BSc in Chemistry in 1995 from Yüzüncü Yıl University, MSc in Biochemistry in 1998, and PhD in Biochemistry in 2002 from Atatürk University, Turkey. He performed post-doctoral studies at Max-Planck Institute, Germany, and University of Florence, Italy in addition to making several scientific visits abroad. He currently works as a Full Professor of Biochemistry in the Faculty of Pharmacy, Anadolu University, Turkey. Dr. Beydemir has published over a hundred scientific papers spanning protein biochemistry, enzymology and medicinal chemistry, reviews, book chapters and presented several conferences to scientists worldwide. He has received numerous publication awards from various international scientific councils. He serves in the Editorial Board of several international journals. Dr. Beydemir is also Rector of Bilecik Şeyh Edebali University, Turkey.",institutionString:null,institution:{name:"Anadolu University",institutionURL:null,country:{name:"Turkey"}}},editorTwo:{id:"13652",title:"Prof.",name:"Deniz",middleName:null,surname:"Ekinci",slug:"deniz-ekinci",fullName:"Deniz Ekinci",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYLT1QAO/Profile_Picture_1634557223079",biography:"Dr. Deniz Ekinci obtained a BSc in Chemistry in 2004, MSc in Biochemistry in 2006, and PhD in Biochemistry in 2009 from Atatürk University, Turkey. He studied at Stetson University, USA, in 2007-2008 and at the Max Planck Institute of Molecular Cell Biology and Genetics, Germany, in 2009-2010. Dr. Ekinci currently works as a Full Professor of Biochemistry in the Faculty of Agriculture and is the Head of the Enzyme and Microbial Biotechnology Division, Ondokuz Mayıs University, Turkey. He is a member of the Turkish Biochemical Society, American Chemical Society, and German Genetics society. Dr. Ekinci published around ninety scientific papers, reviews and book chapters, and presented several conferences to scientists. He has received numerous publication awards from several scientific councils. Dr. Ekinci serves as the Editor in Chief of four international books and is involved in the Editorial Board of several international journals.",institutionString:null,institution:{name:"Ondokuz Mayıs University",institutionURL:null,country:{name:"Turkey"}}},editorThree:null},{id:"17",title:"Metabolism",coverUrl:"https://cdn.intechopen.com/series_topics/covers/17.jpg",isOpenForSubmission:!0,editor:{id:"138626",title:"Dr.",name:"Yannis",middleName:null,surname:"Karamanos",slug:"yannis-karamanos",fullName:"Yannis Karamanos",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002g6Jv2QAE/Profile_Picture_1629356660984",biography:"Yannis Karamanos, born in Greece in 1953, completed his pre-graduate studies at the Université Pierre et Marie Curie, Paris, then his Masters and Doctoral degree at the Université de Lille (1983). He was associate professor at the University of Limoges (1987) before becoming full professor of biochemistry at the Université d’Artois (1996). He worked on the structure-function relationships of glycoconjugates and his main project was the investigations on the biological roles of the de-N-glycosylation enzymes (Endo-N-acetyl-β-D-glucosaminidase and peptide-N4-(N-acetyl-β-glucosaminyl) asparagine amidase). From 2002 he contributes to the understanding of the Blood-brain barrier functioning using proteomics approaches. He has published more than 70 papers. His teaching areas are energy metabolism and regulation, integration and organ specialization and metabolic adaptation.",institutionString:null,institution:{name:"Artois University",institutionURL:null,country:{name:"France"}}},editorTwo:null,editorThree:null},{id:"18",title:"Proteomics",coverUrl:"https://cdn.intechopen.com/series_topics/covers/18.jpg",isOpenForSubmission:!0,editor:{id:"200689",title:"Prof.",name:"Paolo",middleName:null,surname:"Iadarola",slug:"paolo-iadarola",fullName:"Paolo Iadarola",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSCl8QAG/Profile_Picture_1623568118342",biography:"Paolo Iadarola graduated with a degree in Chemistry from the University of Pavia (Italy) in July 1972. He then worked as an Assistant Professor at the Faculty of Science of the same University until 1984. In 1985, Prof. Iadarola became Associate Professor at the Department of Biology and Biotechnologies of the University of Pavia and retired in October 2017. Since then, he has been working as an Adjunct Professor in the same Department at the University of Pavia. His research activity during the first years was primarily focused on the purification and structural characterization of enzymes from animal and plant sources. During this period, Prof. Iadarola familiarized himself with the conventional techniques used in column chromatography, spectrophotometry, manual Edman degradation, and electrophoresis). Since 1995, he has been working on: i) the determination in biological fluids (serum, urine, bronchoalveolar lavage, sputum) of proteolytic activities involved in the degradation processes of connective tissue matrix, and ii) on the identification of biological markers of lung diseases. In this context, he has developed and validated new methodologies (e.g., Capillary Electrophoresis coupled to Laser-Induced Fluorescence, CE-LIF) whose application enabled him to determine both the amounts of biochemical markers (Desmosines) in urine/serum of patients affected by Chronic Obstructive Pulmonary Disease (COPD) and the activity of proteolytic enzymes (Human Neutrophil Elastase, Cathepsin G, Pseudomonas aeruginosa elastase) in sputa of these patients. More recently, Prof. Iadarola was involved in developing techniques such as two-dimensional electrophoresis coupled to liquid chromatography/mass spectrometry (2DE-LC/MS) for the proteomic analysis of biological fluids aimed at the identification of potential biomarkers of different lung diseases. He is the author of about 150 publications (According to Scopus: H-Index: 23; Total citations: 1568- According to WOS: H-Index: 20; Total Citations: 1296) of peer-reviewed international journals. He is a Consultant Reviewer for several journals, including the Journal of Chromatography A, Journal of Chromatography B, Plos ONE, Proteomes, International Journal of Molecular Science, Biotech, Electrophoresis, and others. He is also Associate Editor of Biotech.",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorTwo:{id:"201414",title:"Dr.",name:"Simona",middleName:null,surname:"Viglio",slug:"simona-viglio",fullName:"Simona Viglio",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRKDHQA4/Profile_Picture_1630402531487",biography:"Simona Viglio is an Associate Professor of Biochemistry at the Department of Molecular Medicine at the University of Pavia. She has been working since 1995 on the determination of proteolytic enzymes involved in the degradation process of connective tissue matrix and on the identification of biological markers of lung diseases. She gained considerable experience in developing and validating new methodologies whose applications allowed her to determine both the amount of biomarkers (Desmosine and Isodesmosine) in the urine of patients affected by COPD, and the activity of proteolytic enzymes (HNE, Cathepsin G, Pseudomonas aeruginosa elastase) in the sputa of these patients. Simona Viglio was also involved in research dealing with the supplementation of amino acids in patients with brain injury and chronic heart failure. She is presently engaged in the development of 2-DE and LC-MS techniques for the study of proteomics in biological fluids. The aim of this research is the identification of potential biomarkers of lung diseases. She is an author of about 90 publications (According to Scopus: H-Index: 23; According to WOS: H-Index: 20) on peer-reviewed journals, a member of the “Società Italiana di Biochimica e Biologia Molecolare,“ and a Consultant Reviewer for International Journal of Molecular Science, Journal of Chromatography A, COPD, Plos ONE and Nutritional Neuroscience.",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorThree:null}]},overviewPageOFChapters:{paginationCount:36,paginationItems:[{id:"82195",title:"Endoplasmic Reticulum: A Hub in Lipid Homeostasis",doi:"10.5772/intechopen.105450",signatures:"Raúl Ventura and María Isabel Hernández-Alvarez",slug:"endoplasmic-reticulum-a-hub-in-lipid-homeostasis",totalDownloads:4,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Updates on Endoplasmic Reticulum",coverURL:"https://cdn.intechopen.com/books/images_new/11674.jpg",subseries:{id:"14",title:"Cell and Molecular Biology"}}},{id:"82409",title:"Purinergic Signaling in Covid-19 Disease",doi:"10.5772/intechopen.105008",signatures:"Hailian Shen",slug:"purinergic-signaling-in-covid-19-disease",totalDownloads:5,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Purinergic System",coverURL:"https://cdn.intechopen.com/books/images_new/10801.jpg",subseries:{id:"17",title:"Metabolism"}}},{id:"82374",title:"The Potential of the Purinergic System as a Therapeutic Target of Natural Compounds in Cutaneous Melanoma",doi:"10.5772/intechopen.105457",signatures:"Gilnei Bruno da Silva, Daiane Manica, Marcelo Moreno and Margarete Dulce Bagatini",slug:"the-potential-of-the-purinergic-system-as-a-therapeutic-target-of-natural-compounds-in-cutaneous-mel",totalDownloads:10,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Purinergic System",coverURL:"https://cdn.intechopen.com/books/images_new/10801.jpg",subseries:{id:"17",title:"Metabolism"}}},{id:"82103",title:"The Role of Endoplasmic Reticulum Stress and Its Regulation in the Progression of Neurological and Infectious Diseases",doi:"10.5772/intechopen.105543",signatures:"Mary Dover, Michael Kishek, Miranda Eddins, Naneeta Desar, Ketema Paul and Milan Fiala",slug:"the-role-of-endoplasmic-reticulum-stress-and-its-regulation-in-the-progression-of-neurological-and-i",totalDownloads:6,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Updates on Endoplasmic Reticulum",coverURL:"https://cdn.intechopen.com/books/images_new/11674.jpg",subseries:{id:"14",title:"Cell and Molecular Biology"}}}]},overviewPagePublishedBooks:{paginationCount:32,paginationItems:[{type:"book",id:"7006",title:"Biochemistry and Health Benefits of Fatty Acids",subtitle:null,coverURL:"https://cdn.intechopen.com/books/images_new/7006.jpg",slug:"biochemistry-and-health-benefits-of-fatty-acids",publishedDate:"December 19th 2018",editedByType:"Edited by",bookSignature:"Viduranga Waisundara",hash:"c93a00abd68b5eba67e5e719f67fd20b",volumeInSeries:1,fullTitle:"Biochemistry and Health Benefits of Fatty Acids",editors:[{id:"194281",title:"Dr.",name:"Viduranga Y.",middleName:null,surname:"Waisundara",slug:"viduranga-y.-waisundara",fullName:"Viduranga Y. Waisundara",profilePictureURL:"https://mts.intechopen.com/storage/users/194281/images/system/194281.jpg",biography:"Dr. Viduranga Waisundara obtained her Ph.D. in Food Science\nand Technology from the Department of Chemistry, National\nUniversity of Singapore, in 2010. She was a lecturer at Temasek Polytechnic, Singapore from July 2009 to March 2013.\nShe relocated to her motherland of Sri Lanka and spearheaded the Functional Food Product Development Project at the\nNational Institute of Fundamental Studies from April 2013 to\nOctober 2016. She was a senior lecturer on a temporary basis at the Department of\nFood Technology, Faculty of Technology, Rajarata University of Sri Lanka. She is\ncurrently Deputy Principal of the Australian College of Business and Technology –\nKandy Campus, Sri Lanka. 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Since 1983, he has been a faculty member of the RO Perelman Department of Dermatology, NYU School of Medicine, where he is codirector of a training grant in cutaneous biology. Dr. Blumenberg’s research is focused on the epidermis, expression of keratin genes, transcription profiling, keratinocyte differentiation, inflammatory diseases and cancers, and most recently the effects of the microbiome on the skin. 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She has more than fifteen years of teaching and research experience. She has published more than 550 scientific publications/communications, including 15 books, 50 book chapters, 100 original research papers, 380 research communications in national and international conferences, and 12 patents. She is a member of the editorial board of five journals and acts as a reviewer for several national and international journals. Her research interests include microalgal biotechnology with an emphasis on microalgae-based products.",institutionString:"Universidade Federal de Santa Maria",institution:{name:"Universidade Federal de Santa Maria",institutionURL:null,country:{name:"Brazil"}}}]},{type:"book",id:"7953",title:"Bioluminescence",subtitle:"Analytical Applications and Basic Biology",coverURL:"https://cdn.intechopen.com/books/images_new/7953.jpg",slug:"bioluminescence-analytical-applications-and-basic-biology",publishedDate:"September 25th 2019",editedByType:"Edited by",bookSignature:"Hirobumi Suzuki",hash:"3a8efa00b71abea11bf01973dc589979",volumeInSeries:4,fullTitle:"Bioluminescence - Analytical Applications and Basic Biology",editors:[{id:"185746",title:"Dr.",name:"Hirobumi",middleName:null,surname:"Suzuki",slug:"hirobumi-suzuki",fullName:"Hirobumi Suzuki",profilePictureURL:"https://mts.intechopen.com/storage/users/185746/images/system/185746.png",biography:"Dr. Hirobumi Suzuki received his Ph.D. in 1997 from Tokyo Metropolitan University, Japan, where he studied firefly phylogeny and the evolution of mating systems. He is especially interested in the genetic differentiation pattern and speciation process that correlate to the flashing pattern and mating behavior of some fireflies in Japan. He then worked for Olympus Corporation, a Japanese manufacturer of optics and imaging products, where he was involved in the development of luminescence technology and produced a bioluminescence microscope that is currently being used for gene expression analysis in chronobiology, neurobiology, and developmental biology. 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Dr. Şentürk serves as the editorial board member of several international journals.",institutionString:"Ağrı İbrahim Çeçen University",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"2",totalChapterViews:"0",totalEditedBooks:"1",institution:{name:"Ağrı İbrahim Çeçen University",institutionURL:null,country:{name:"Turkey"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null}],selectedSeries:{id:"11",title:"Biochemistry"},selectedSubseries:{id:"18",title:"Proteomics",coverUrl:"https://cdn.intechopen.com/series_topics/covers/18.jpg",editor:{id:"200689",title:"Prof.",name:"Paolo",middleName:null,surname:"Iadarola",slug:"paolo-iadarola",fullName:"Paolo Iadarola",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSCl8QAG/Profile_Picture_1623568118342",biography:"Paolo Iadarola graduated with a degree in Chemistry from the University of Pavia (Italy) in July 1972. He then worked as an Assistant Professor at the Faculty of Science of the same University until 1984. In 1985, Prof. Iadarola became Associate Professor at the Department of Biology and Biotechnologies of the University of Pavia and retired in October 2017. Since then, he has been working as an Adjunct Professor in the same Department at the University of Pavia. His research activity during the first years was primarily focused on the purification and structural characterization of enzymes from animal and plant sources. During this period, Prof. Iadarola familiarized himself with the conventional techniques used in column chromatography, spectrophotometry, manual Edman degradation, and electrophoresis). Since 1995, he has been working on: i) the determination in biological fluids (serum, urine, bronchoalveolar lavage, sputum) of proteolytic activities involved in the degradation processes of connective tissue matrix, and ii) on the identification of biological markers of lung diseases. In this context, he has developed and validated new methodologies (e.g., Capillary Electrophoresis coupled to Laser-Induced Fluorescence, CE-LIF) whose application enabled him to determine both the amounts of biochemical markers (Desmosines) in urine/serum of patients affected by Chronic Obstructive Pulmonary Disease (COPD) and the activity of proteolytic enzymes (Human Neutrophil Elastase, Cathepsin G, Pseudomonas aeruginosa elastase) in sputa of these patients. More recently, Prof. Iadarola was involved in developing techniques such as two-dimensional electrophoresis coupled to liquid chromatography/mass spectrometry (2DE-LC/MS) for the proteomic analysis of biological fluids aimed at the identification of potential biomarkers of different lung diseases. He is the author of about 150 publications (According to Scopus: H-Index: 23; Total citations: 1568- According to WOS: H-Index: 20; Total Citations: 1296) of peer-reviewed international journals. He is a Consultant Reviewer for several journals, including the Journal of Chromatography A, Journal of Chromatography B, Plos ONE, Proteomes, International Journal of Molecular Science, Biotech, Electrophoresis, and others. He is also Associate Editor of Biotech.",institutionString:null,position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"2",totalChapterViews:"0",totalEditedBooks:"0",institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorTwo:{id:"201414",title:"Dr.",name:"Simona",middleName:null,surname:"Viglio",slug:"simona-viglio",fullName:"Simona Viglio",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRKDHQA4/Profile_Picture_1630402531487",biography:"Simona Viglio is an Associate Professor of Biochemistry at the Department of Molecular Medicine at the University of Pavia. She has been working since 1995 on the determination of proteolytic enzymes involved in the degradation process of connective tissue matrix and on the identification of biological markers of lung diseases. She gained considerable experience in developing and validating new methodologies whose applications allowed her to determine both the amount of biomarkers (Desmosine and Isodesmosine) in the urine of patients affected by COPD, and the activity of proteolytic enzymes (HNE, Cathepsin G, Pseudomonas aeruginosa elastase) in the sputa of these patients. Simona Viglio was also involved in research dealing with the supplementation of amino acids in patients with brain injury and chronic heart failure. She is presently engaged in the development of 2-DE and LC-MS techniques for the study of proteomics in biological fluids. The aim of this research is the identification of potential biomarkers of lung diseases. She is an author of about 90 publications (According to Scopus: H-Index: 23; According to WOS: H-Index: 20) on peer-reviewed journals, a member of the “Società Italiana di Biochimica e Biologia Molecolare,“ and a Consultant Reviewer for International Journal of Molecular Science, Journal of Chromatography A, COPD, Plos ONE and Nutritional Neuroscience.",institutionString:null,position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"2",totalChapterViews:"0",totalEditedBooks:"0",institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorThree:null,series:{id:"11",title:"Biochemistry"}}},seriesLanding:{item:{id:"11",title:"Biochemistry",doi:"10.5772/intechopen.72877",issn:"2632-0983",scope:"Biochemistry, the study of chemical transformations occurring within living organisms, impacts all areas of life sciences, from molecular crystallography and genetics to ecology, medicine, and population biology. Biochemistry examines macromolecules - proteins, nucleic acids, carbohydrates, and lipids – and their building blocks, structures, functions, and interactions. Much of biochemistry is devoted to enzymes, proteins that catalyze chemical reactions, enzyme structures, mechanisms of action and their roles within cells. Biochemistry also studies small signaling molecules, coenzymes, inhibitors, vitamins, and hormones, which play roles in life processes. Biochemical experimentation, besides coopting classical chemistry methods, e.g., chromatography, adopted new techniques, e.g., X-ray diffraction, electron microscopy, NMR, radioisotopes, and developed sophisticated microbial genetic tools, e.g., auxotroph mutants and their revertants, fermentation, etc. More recently, biochemistry embraced the ‘big data’ omics systems. Initial biochemical studies have been exclusively analytic: dissecting, purifying, and examining individual components of a biological system; in the apt words of Efraim Racker (1913 –1991), “Don’t waste clean thinking on dirty enzymes.” Today, however, biochemistry is becoming more agglomerative and comprehensive, setting out to integrate and describe entirely particular biological systems. The ‘big data’ metabolomics can define the complement of small molecules, e.g., in a soil or biofilm sample; proteomics can distinguish all the comprising proteins, e.g., serum; metagenomics can identify all the genes in a complex environment, e.g., the bovine rumen. This Biochemistry Series will address the current research on biomolecules and the emerging trends with great promise.",coverUrl:"https://cdn.intechopen.com/series/covers/11.jpg",latestPublicationDate:"June 29th, 2022",hasOnlineFirst:!0,numberOfOpenTopics:4,numberOfPublishedChapters:318,numberOfPublishedBooks:32,editor:{id:"31610",title:"Dr.",name:"Miroslav",middleName:null,surname:"Blumenberg",fullName:"Miroslav Blumenberg",profilePictureURL:"https://mts.intechopen.com/storage/users/31610/images/system/31610.jpg",biography:"Miroslav Blumenberg, Ph.D., was born in Subotica and received his BSc in Belgrade, Yugoslavia. He completed his Ph.D. at MIT in Organic Chemistry; he followed up his Ph.D. with two postdoctoral study periods at Stanford University. Since 1983, he has been a faculty member of the RO Perelman Department of Dermatology, NYU School of Medicine, where he is codirector of a training grant in cutaneous biology. Dr. Blumenberg’s research is focused on the epidermis, expression of keratin genes, transcription profiling, keratinocyte differentiation, inflammatory diseases and cancers, and most recently the effects of the microbiome on the skin. He has published more than 100 peer-reviewed research articles and graduated numerous Ph.D. and postdoctoral students.",institutionString:null,institution:{name:"New York University Langone Medical Center",institutionURL:null,country:{name:"United States of America"}}},subseries:[{id:"14",title:"Cell and Molecular Biology",keywords:"Omics (Transcriptomics; Proteomics; Metabolomics), Molecular Biology, Cell Biology, Signal Transduction and Regulation, Cell Growth and Differentiation, Apoptosis, Necroptosis, Ferroptosis, Autophagy, Cell Cycle, Macromolecules and Complexes, Gene Expression",scope:"The Cell and Molecular Biology topic within the IntechOpen Biochemistry Series aims to rapidly publish contributions on all aspects of cell and molecular biology, including aspects related to biochemical and genetic research (not only in humans but all living beings). We encourage the submission of manuscripts that provide novel and mechanistic insights that report significant advances in the fields. Topics include, but are not limited to: Advanced techniques of cellular and molecular biology (Molecular methodologies, imaging techniques, and bioinformatics); Biological activities at the molecular level; Biological processes of cell functions, cell division, senescence, maintenance, and cell death; Biomolecules interactions; Cancer; Cell biology; Chemical biology; Computational biology; Cytochemistry; Developmental biology; Disease mechanisms and therapeutics; DNA, and RNA metabolism; Gene functions, genetics, and genomics; Genetics; Immunology; Medical microbiology; Molecular biology; Molecular genetics; Molecular processes of cell and organelle dynamics; Neuroscience; Protein biosynthesis, degradation, and functions; Regulation of molecular interactions in a cell; Signalling networks and system biology; Structural biology; Virology and microbiology.",annualVolume:11410,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/14.jpg",editor:{id:"165627",title:"Dr.",name:"Rosa María",middleName:null,surname:"Martínez-Espinosa",fullName:"Rosa María Martínez-Espinosa",profilePictureURL:"https://mts.intechopen.com/storage/users/165627/images/system/165627.jpeg",institutionString:null,institution:{name:"University of Alicante",institutionURL:null,country:{name:"Spain"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"79367",title:"Dr.",name:"Ana Isabel",middleName:null,surname:"Flores",fullName:"Ana Isabel Flores",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRpIOQA0/Profile_Picture_1632418099564",institutionString:null,institution:{name:"Hospital Universitario 12 De Octubre",institutionURL:null,country:{name:"Spain"}}},{id:"328234",title:"Ph.D.",name:"Christian",middleName:null,surname:"Palavecino",fullName:"Christian Palavecino",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000030DhEhQAK/Profile_Picture_1628835318625",institutionString:null,institution:{name:"Central University of Chile",institutionURL:null,country:{name:"Chile"}}},{id:"186585",title:"Dr.",name:"Francisco Javier",middleName:null,surname:"Martin-Romero",fullName:"Francisco Javier Martin-Romero",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSB3HQAW/Profile_Picture_1631258137641",institutionString:null,institution:{name:"University of Extremadura",institutionURL:null,country:{name:"Spain"}}}]},{id:"15",title:"Chemical Biology",keywords:"Phenolic Compounds, Essential Oils, Modification of Biomolecules, Glycobiology, Combinatorial Chemistry, Therapeutic peptides, Enzyme Inhibitors",scope:"Chemical biology spans the fields of chemistry and biology involving the application of biological and chemical molecules and techniques. In recent years, the application of chemistry to biological molecules has gained significant interest in medicinal and pharmacological studies. This topic will be devoted to understanding the interplay between biomolecules and chemical compounds, their structure and function, and their potential applications in related fields. Being a part of the biochemistry discipline, the ideas and concepts that have emerged from Chemical Biology have affected other related areas. This topic will closely deal with all emerging trends in this discipline.",annualVolume:11411,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/15.jpg",editor:{id:"441442",title:"Dr.",name:"Şükrü",middleName:null,surname:"Beydemir",fullName:"Şükrü Beydemir",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00003GsUoIQAV/Profile_Picture_1634557147521",institutionString:null,institution:{name:"Anadolu University",institutionURL:null,country:{name:"Turkey"}}},editorTwo:{id:"13652",title:"Prof.",name:"Deniz",middleName:null,surname:"Ekinci",fullName:"Deniz Ekinci",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYLT1QAO/Profile_Picture_1634557223079",institutionString:null,institution:{name:"Ondokuz Mayıs University",institutionURL:null,country:{name:"Turkey"}}},editorThree:null,editorialBoard:[{id:"219081",title:"Dr.",name:"Abdulsamed",middleName:null,surname:"Kükürt",fullName:"Abdulsamed Kükürt",profilePictureURL:"https://mts.intechopen.com/storage/users/219081/images/system/219081.png",institutionString:null,institution:{name:"Kafkas University",institutionURL:null,country:{name:"Turkey"}}},{id:"241413",title:"Dr.",name:"Azhar",middleName:null,surname:"Rasul",fullName:"Azhar Rasul",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRT1oQAG/Profile_Picture_1635251978933",institutionString:null,institution:{name:"Government College University, Faisalabad",institutionURL:null,country:{name:"Pakistan"}}},{id:"178316",title:"Ph.D.",name:"Sergey",middleName:null,surname:"Sedykh",fullName:"Sergey Sedykh",profilePictureURL:"https://mts.intechopen.com/storage/users/178316/images/system/178316.jfif",institutionString:null,institution:{name:"Novosibirsk State University",institutionURL:null,country:{name:"Russia"}}}]},{id:"17",title:"Metabolism",keywords:"Biomolecules Metabolism, Energy Metabolism, Metabolic Pathways, Key Metabolic Enzymes, Metabolic Adaptation",scope:"Metabolism is frequently defined in biochemistry textbooks as the overall process that allows living systems to acquire and use the free energy they need for their vital functions or the chemical processes that occur within a living organism to maintain life. Behind these definitions are hidden all the aspects of normal and pathological functioning of all processes that the topic ‘Metabolism’ will cover within the Biochemistry Series. Thus all studies on metabolism will be considered for publication.",annualVolume:11413,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/17.jpg",editor:{id:"138626",title:"Dr.",name:"Yannis",middleName:null,surname:"Karamanos",fullName:"Yannis Karamanos",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002g6Jv2QAE/Profile_Picture_1629356660984",institutionString:null,institution:{name:"Artois University",institutionURL:null,country:{name:"France"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"243049",title:"Dr.",name:"Anca",middleName:null,surname:"Pantea Stoian",fullName:"Anca Pantea Stoian",profilePictureURL:"https://mts.intechopen.com/storage/users/243049/images/system/243049.jpg",institutionString:null,institution:{name:"Carol Davila University of Medicine and Pharmacy",institutionURL:null,country:{name:"Romania"}}},{id:"203824",title:"Dr.",name:"Attilio",middleName:null,surname:"Rigotti",fullName:"Attilio Rigotti",profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institutionString:null,institution:{name:"Pontifical Catholic University of Chile",institutionURL:null,country:{name:"Chile"}}},{id:"300470",title:"Dr.",name:"Yanfei (Jacob)",middleName:null,surname:"Qi",fullName:"Yanfei (Jacob) Qi",profilePictureURL:"https://mts.intechopen.com/storage/users/300470/images/system/300470.jpg",institutionString:null,institution:{name:"Centenary Institute of Cancer Medicine and Cell Biology",institutionURL:null,country:{name:"Australia"}}}]},{id:"18",title:"Proteomics",keywords:"Mono- and Two-Dimensional Gel Electrophoresis (1-and 2-DE), Liquid Chromatography (LC), Mass Spectrometry/Tandem Mass Spectrometry (MS; MS/MS), Proteins",scope:"With the recognition that the human genome cannot provide answers to the etiology of a disorder, changes in the proteins expressed by a genome became a focus in research. Thus proteomics, an area of research that detects all protein forms expressed in an organism, including splice isoforms and post-translational modifications, is more suitable than genomics for a comprehensive understanding of the biochemical processes that govern life. The most common proteomics applications are currently in the clinical field for the identification, in a variety of biological matrices, of biomarkers for diagnosis and therapeutic intervention of disorders. From the comparison of proteomic profiles of control and disease or different physiological states, which may emerge, changes in protein expression can provide new insights into the roles played by some proteins in human pathologies. Understanding how proteins function and interact with each other is another goal of proteomics that makes this approach even more intriguing. Specialized technology and expertise are required to assess the proteome of any biological sample. Currently, proteomics relies mainly on mass spectrometry (MS) combined with electrophoretic (1 or 2-DE-MS) and/or chromatographic techniques (LC-MS/MS). MS is an excellent tool that has gained popularity in proteomics because of its ability to gather a complex body of information such as cataloging protein expression, identifying protein modification sites, and defining protein interactions. The Proteomics topic aims to attract contributions on all aspects of MS-based proteomics that, by pushing the boundaries of MS capabilities, may address biological problems that have not been resolved yet.",annualVolume:11414,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/18.jpg",editor:{id:"200689",title:"Prof.",name:"Paolo",middleName:null,surname:"Iadarola",fullName:"Paolo Iadarola",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSCl8QAG/Profile_Picture_1623568118342",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorTwo:{id:"201414",title:"Dr.",name:"Simona",middleName:null,surname:"Viglio",fullName:"Simona Viglio",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRKDHQA4/Profile_Picture_1630402531487",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorThree:null,editorialBoard:[{id:"72288",title:"Dr.",name:"Arli Aditya",middleName:null,surname:"Parikesit",fullName:"Arli Aditya Parikesit",profilePictureURL:"https://mts.intechopen.com/storage/users/72288/images/system/72288.jpg",institutionString:null,institution:{name:"Indonesia International Institute for Life Sciences",institutionURL:null,country:{name:"Indonesia"}}},{id:"40928",title:"Dr.",name:"Cesar",middleName:null,surname:"Lopez-Camarillo",fullName:"Cesar Lopez-Camarillo",profilePictureURL:"https://mts.intechopen.com/storage/users/40928/images/3884_n.png",institutionString:null,institution:{name:"Universidad Autónoma de la Ciudad de México",institutionURL:null,country:{name:"Mexico"}}},{id:"81926",title:"Dr.",name:"Shymaa",middleName:null,surname:"Enany",fullName:"Shymaa Enany",profilePictureURL:"https://mts.intechopen.com/storage/users/81926/images/system/81926.png",institutionString:"Suez Canal University",institution:{name:"Suez Canal University",institutionURL:null,country:{name:"Egypt"}}}]}]}},libraryRecommendation:{success:null,errors:{},institutions:[]},route:{name:"chapter.detail",path:"/chapters/65281",hash:"",query:{},params:{id:"65281"},fullPath:"/chapters/65281",meta:{},from:{name:null,path:"/",hash:"",query:{},params:{},fullPath:"/",meta:{}}}},function(){var e;(e=document.currentScript||document.scripts[document.scripts.length-1]).parentNode.removeChild(e)}()