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Barely three months into the new year and we are happy to announce a monumental milestone reached - 150 million downloads.
\n\nThis achievement solidifies IntechOpen’s place as a pioneer in Open Access publishing and the home to some of the most relevant scientific research available through Open Access.
\n\nWe are so proud to have worked with so many bright minds throughout the years who have helped us spread knowledge through the power of Open Access and we look forward to continuing to support some of the greatest thinkers of our day.
\n\nThank you for making IntechOpen your place of learning, sharing, and discovery, and here’s to 150 million more!
\n\n\n\n\n'}],latestNews:[{slug:"intechopen-supports-asapbio-s-new-initiative-publish-your-reviews-20220729",title:"IntechOpen Supports ASAPbio’s New Initiative Publish Your Reviews"},{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"}]},book:{item:{type:"book",id:"7870",leadTitle:null,fullTitle:"Muscle Cells - Recent Advances and Future Perspectives",title:"Muscle Cells",subtitle:"Recent Advances and Future Perspectives",reviewType:"peer-reviewed",abstract:"The three different types of muscle tissue found in the animal kingdom are cardiac, skeletal, and smooth. The muscle cells are not only complex but also fascinating. In recent years there has been substantial advances in our understanding of muscle cell biology, especially in areas of molecular anatomy, basic physiology, understanding disease mechanisms, and therapeutic targets. Consequently, this book mainly focuses not only on the biology of myocytes, but also on all-encompassing disciplines pertaining to muscle tissue, such as fundamental physiology, molecular mechanisms of diseases, muscle regeneration, etc. for all three types of muscle, namely, skeletal, cardiac, and smooth muscle. As a result, the goal of this book is to consolidate the recent advances in the area of muscle biology/diseases/regeneration covering a broad range of interrelated topics in a timely fashion and to disseminate that knowledge in a lucid way to a greater scientific audience. This book will prove highly useful for students, researchers, and clinicians in muscle cell biology, exercise physiology/science, stem cell biology, developmental biology, cancer biology, pathology, oncology, as well as tissue engineering and regenerative medicine. This quick reference will benefit anyone desiring a thorough knowledge pertaining to recent advances in muscle biology in the context of health and disease.",isbn:"978-1-78923-968-3",printIsbn:"978-1-78923-967-6",pdfIsbn:"978-1-83968-010-6",doi:"10.5772/intechopen.77689",price:119,priceEur:129,priceUsd:155,slug:"muscle-cells-recent-advances-and-future-perspectives",numberOfPages:180,isOpenForSubmission:!1,isInWos:null,isInBkci:!1,hash:"64634d90d737661d1e606cac28b79969",bookSignature:"Mani T. Valarmathi",publishedDate:"January 22nd 2020",coverURL:"https://cdn.intechopen.com/books/images_new/7870.jpg",numberOfDownloads:7194,numberOfWosCitations:1,numberOfCrossrefCitations:4,numberOfCrossrefCitationsByBook:1,numberOfDimensionsCitations:8,numberOfDimensionsCitationsByBook:1,hasAltmetrics:1,numberOfTotalCitations:13,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"September 6th 2018",dateEndSecondStepPublish:"November 6th 2018",dateEndThirdStepPublish:"January 5th 2019",dateEndFourthStepPublish:"March 26th 2019",dateEndFifthStepPublish:"May 25th 2019",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"69697",title:"Dr.",name:"Mani T.",middleName:null,surname:"Valarmathi",slug:"mani-t.-valarmathi",fullName:"Mani T. Valarmathi",profilePictureURL:"https://mts.intechopen.com/storage/users/69697/images/system/69697.jpg",biography:"Mani T. Valarmathi is currently Director of Research and Development at Religen Inc., a life science company in Pennsylvania, USA. He began his scientific career as a cancer geneticist but soon became captivated with the emerging and translational fields of stem cell biology, tissue engineering, and regenerative medicine. After obtaining a bachelor’s degree in Chemistry from the University of Madras, Chennai, Tamil Nadu, India, he obtained an MBBS in Medicine and Surgery and an MD in Pathology from the same university. Dr. Valarmathi also holds a Ph.D. in Medical Biotechnology from the All-India Institute of Medical Sciences, New Delhi, India. Over the past two decades, he has had extensive experience in research on various types of stem cells, focused on creating bioengineered human 3D vascularized tissues constructs for implantation purposes. At present, much of his research is directed towards developing innovative molecular genetic testing for precision and genetic medicine. He is a member of many prestigious national and international professional societies and scientific organizations, including the International Society for Stem Cell Research (ISSCR), Tissue Engineering and Regenerative Medicine International Society (TERMIS), American Association for Cancer Research (AACR), American Society for Investigative Pathology (ASIP), American Society for Clinical Pathology (ASCP), American Chemical Society (ACS), European Society of Cardiology (ESC), International Society for Heart Research (ISHR), American Society of Gene & Cell Therapy (ASGCT), and American Heart Association (AHA).",institutionString:"Religen Inc. | A Life Science Company, United States of America",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"3",totalChapterViews:"0",totalEditedBooks:"4",institution:null}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"1064",title:"Human Anatomy",slug:"human-anatomy"}],chapters:[{id:"66964",title:"Vascularisation of Skeletal Muscle",doi:"10.5772/intechopen.85903",slug:"vascularisation-of-skeletal-muscle",totalDownloads:943,totalCrossrefCites:0,totalDimensionsCites:3,hasAltmetrics:0,abstract:"Skeletal muscle is mainly involved in physical activity and movement, which requires a large amount of glucose, fatty acids, and oxygen. These materials are supplied by blood vessels and incorporated into the muscle fiber through the cell membrane. In contrast, metabolic waste is discarded outside the cell membrane and removed by blood vessels. The formation of a functional, integrated vascular network is a fundamental process in the growth and maintenance of skeletal muscle. On the other hand, vascularization is one of the main central components in skeletal muscle regeneration. In order for regeneration to occur, blood vessels must invade the transplanted muscle. This is confirmed by the fact that muscle regeneration occurred from the outside of the muscle bundle toward the inner regions. In fact, it is likely that capillary formation is a key process to start muscle regeneration. Thus, vascularization activates muscle regeneration, and a decrease in vascularization could lead to disruption the process of muscle regeneration. Also, a better understanding of vascularization of skeletal muscle necessary for the successful formation of collateral arteries and recovery of injured skeletal muscle may lead to more successful strategies for skeletal muscle regeneration and engineering. So, in this chapter, we want to review vascularization in skeletal muscle.",signatures:"Kamal Ranjbar and Bayan Fayazi",downloadPdfUrl:"/chapter/pdf-download/66964",previewPdfUrl:"/chapter/pdf-preview/66964",authors:[{id:"143655",title:"Ph.D. Student",name:"Kamal",surname:"Ranjbar",slug:"kamal-ranjbar",fullName:"Kamal Ranjbar"},{id:"299168",title:"Dr.",name:"Bayan",surname:"Fayazi",slug:"bayan-fayazi",fullName:"Bayan Fayazi"}],corrections:null},{id:"66080",title:"Excitability of Vascular Smooth Muscle",doi:"10.5772/intechopen.85053",slug:"excitability-of-vascular-smooth-muscle",totalDownloads:890,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Regulation of pressure and local blood flow occurs at the level of resistance arteries and arterioles. Under physiological conditions, these small vessels exist in a state of partial constriction, termed myogenic tone. Myogenic tone is considered to be an intrinsic property of arteriolar smooth muscle cells, which membranes depolarize in response to increase in the intraluminal pressure. Oscillations of membrane potential in smooth muscles are mediated by the activity of voltage-gated L-type Ca2+ channels, which provide an influx of Ca2+ to activate various voltage-gated and Ca2+-sensitive channels of smooth muscle cells and to initiate endothelial Ca2+ signaling needed for vasodilation. Although a relationship between change in membrane potential and myogenic response is considered to be universal throughout various smooth muscle tissues, it may be regulated differently based on autoregulatory responses and channels expression. Here we review electrophysiological signature of arteriolar smooth muscle in various tissues, with an emphases and specific examples of the excitability of 4th order arterioles isolated from skeletal muscle.",signatures:"Alexandra V. Ulyanova",downloadPdfUrl:"/chapter/pdf-download/66080",previewPdfUrl:"/chapter/pdf-preview/66080",authors:[{id:"273990",title:"Dr.",name:"Alexandra V.",surname:"Ulyanova",slug:"alexandra-v.-ulyanova",fullName:"Alexandra V. Ulyanova"}],corrections:null},{id:"66388",title:"Orexin System and Avian Muscle Mitochondria",doi:"10.5772/intechopen.85177",slug:"orexin-system-and-avian-muscle-mitochondria",totalDownloads:873,totalCrossrefCites:2,totalDimensionsCites:3,hasAltmetrics:0,abstract:"In mammals, orexin A and B (also known as hypocretin 1 and 2) are two orexigenic peptides produced primarily by the lateral hypothalamus that signal through two G-protein-coupled receptors, orexin receptors 1/2, and have been implicated in the regulation of several physiological processes. However, the physiological roles of orexin are not well defined in avian (non-mammalian vertebrate) species. Recently, we made a breakthrough by identifying that orexin and its related receptors 1/2 (ORXR1/2) are expressed in avian muscle tissue and cell line, and appears to be a secretory protein. Functional in vitro studies showed that orexin A and B differentially regulated expression of the orexin system, suggesting that orexins might have autocrine, paracrine, and/or endocrine roles. Administration of recombinant orexin modulated mitochondrial biogenesis, dynamics, function, and bioenergetics. In this chapter, we include a brief overview of the (patho) physiological role of orexin, comparative findings between mammalian and avian orexin, and in-depth analysis of orexin’s action on avian muscle mitochondria.",signatures:"Kentu Lassiter and Sami Dridi",downloadPdfUrl:"/chapter/pdf-download/66388",previewPdfUrl:"/chapter/pdf-preview/66388",authors:[{id:"274577",title:"Ph.D. Student",name:"Kentu",surname:"Lassiter",slug:"kentu-lassiter",fullName:"Kentu Lassiter"},{id:"274579",title:"Dr.",name:"Sami",surname:"Dridi",slug:"sami-dridi",fullName:"Sami Dridi"}],corrections:null},{id:"68901",title:"Noncoding RNAs in the Cardiovascular System: Exercise Training Effects",doi:"10.5772/intechopen.86054",slug:"noncoding-rnas-in-the-cardiovascular-system-exercise-training-effects",totalDownloads:712,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Exercise training (ET) represents a non-pharmacological treatment that can attenuate or even reverse the process of cardiovascular diseases (CVD), by stimulating protein synthesis, angiogenesis, mitochondrial biogenesis, anti-inflammatory, and anti-oxidative effects that are involved to enhance the performance and improved quality of life. Despite the benefits of exercise, the intricacies of their underlying molecular mechanisms remain largely unknown. Noncoding RNAs (ncRNAs) have been recognized as a major regulatory network governing gene expression in several physiological processes and appeared as pivotal modulators in a myriad of cardiovascular processes under physiological and pathological conditions. However, little is known about ncRNA expression and role in response to exercise. Here we review the current understanding of the ncRNA role in exercise-induced adaptations focused on the cardiovascular system and address their potential role in clinical applications for cardiovascular diseases.",signatures:"Noemy Pereira, Camila Gatto, Edilamar Menezes de Oliveira and Tiago Fernandes",downloadPdfUrl:"/chapter/pdf-download/68901",previewPdfUrl:"/chapter/pdf-preview/68901",authors:[{id:"60681",title:"Dr.",name:"Edilamar Menezes",surname:"de Oliveira",slug:"edilamar-menezes-de-oliveira",fullName:"Edilamar Menezes de Oliveira"},{id:"144084",title:"Ph.D.",name:"Tiago",surname:"Fernandes",slug:"tiago-fernandes",fullName:"Tiago Fernandes"},{id:"277999",title:"MSc.",name:"Noemy",surname:"Pereira",slug:"noemy-pereira",fullName:"Noemy Pereira"},{id:"278002",title:"MSc.",name:"Camila",surname:"Gatto",slug:"camila-gatto",fullName:"Camila Gatto"}],corrections:null},{id:"67281",title:"Inflammatory Muscle Diseases",doi:"10.5772/intechopen.86053",slug:"inflammatory-muscle-diseases",totalDownloads:907,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Inflammatory myopathies, also called idiopathic inflammatory myopathy or myositis, are rare conditions characterized by the involvement of various organs in addition to muscle tissue. These changes can lead to severe impairments and adversely impact the quality of life of affected individuals. The diagnosis and treatment of inflammatory myopathies involve the participation of an interdisciplinary team, due to the complexity of the disease and the high variety of possible signs and symptoms. In this chapter we will discuss the epidemiology and characteristics of the main subtypes of inflammatory myopathies, such as polymyositis, dermatomyositis, necrotizing myopathy, overlap myositis, and myositis of inclusion bodies. Next, we will discuss the existence of crosstalk between inflammatory processes in the oral cavity and their consequences on skeletal muscle. As oral inflammation can increase infiltration of macrophages in muscle tissue and this increase is related to the production of proinflammatory cytokines in this tissue, these cytokines can cause muscle weakness. It is important to consider the prevention of chronic inflammatory processes in order to maintain muscle integrity or even prevent the worsening of the clinical condition of patients with inflammatory muscle diseases.",signatures:"Doris Hissako Sumida, Fernando Yamamoto Chiba and Maria Sara de Lima Coutinho Mattera",downloadPdfUrl:"/chapter/pdf-download/67281",previewPdfUrl:"/chapter/pdf-preview/67281",authors:[{id:"283757",title:"Prof.",name:"Doris Hissako",surname:"Sumida",slug:"doris-hissako-sumida",fullName:"Doris Hissako Sumida"},{id:"294070",title:"Dr.",name:"Fernando Yamamoto",surname:"Chiba",slug:"fernando-yamamoto-chiba",fullName:"Fernando Yamamoto Chiba"},{id:"294072",title:"MSc.",name:"Maria Sara De Lima Coutinho",surname:"Mattera",slug:"maria-sara-de-lima-coutinho-mattera",fullName:"Maria Sara De Lima Coutinho Mattera"}],corrections:null},{id:"62090",title:"Leucine and Its Importance for Cell Signalling Pathways in Cancer Cachexia-Induced Muscle Wasting",doi:"10.5772/intechopen.78990",slug:"leucine-and-its-importance-for-cell-signalling-pathways-in-cancer-cachexia-induced-muscle-wasting",totalDownloads:1038,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"The anabolic effects of a supplemented diet with branched-chain amino acids, especially leucine, on skeletal muscle wasting and as a co-adjuvant in cancer treatment have been well-studied. Leucine is a precursor of protein synthesis and acts as a nutritional signal, affecting multiple metabolic processes (e.g., satiety, thermogenesis, energy efficiency, and body composition). Previous studies related to nutritional therapy have mainly focused on myopenia, which is the loss of skeletal muscle mass in some pathologies, including cancer. Leucine plays a role in the maintenance and even increase of lean body mass in healthy individuals as well as the prevention of disease states that culminate in myopenia. Herein, we review the available data addressing the mechanisms by which leucine acts as a cellular signal, thereby stimulating muscle protein synthesis, leading to the inhibition of muscle catabolism, especially in an experimental model of cancer cachexia. We also show differences found in the metabolomic and proteomic analyses, including the use of leucine in maternal diets as a preventative for muscle wasting as supported by our experimental data.",signatures:"Andre Gustavo Oliveira, Bread Cruz, Sarah Christine Pereira de Oliveira, Lais Rosa Viana, Natalia Angelo Da Silva Miyaguti, Luiz Alberto Ferreira Ramos, Rafael Rossi Valentim and Maria Cristina Cintra Gomes-Marcondes",downloadPdfUrl:"/chapter/pdf-download/62090",previewPdfUrl:"/chapter/pdf-preview/62090",authors:[{id:"242462",title:"Prof.",name:"Maria Cristina Cintra",surname:"Gomes-Marcondes",slug:"maria-cristina-cintra-gomes-marcondes",fullName:"Maria Cristina Cintra Gomes-Marcondes"},{id:"243467",title:"Dr.",name:"Lais Rosa",surname:"Viana",slug:"lais-rosa-viana",fullName:"Lais Rosa Viana"},{id:"243468",title:"Dr.",name:"Andre Gustavo",surname:"Oliveira",slug:"andre-gustavo-oliveira",fullName:"Andre Gustavo Oliveira"},{id:"243470",title:"Dr.",name:"Bread",surname:"Cruz",slug:"bread-cruz",fullName:"Bread Cruz"},{id:"243471",title:"Dr.",name:"Rafael",surname:"Rossi Valentim",slug:"rafael-rossi-valentim",fullName:"Rafael Rossi Valentim"},{id:"243472",title:"Dr.",name:"Luiz Alberto",surname:"Ferreira Ramos",slug:"luiz-alberto-ferreira-ramos",fullName:"Luiz Alberto Ferreira Ramos"},{id:"243767",title:"MSc.",name:"Natalia Angelo Da Silva",surname:"Miyaguti",slug:"natalia-angelo-da-silva-miyaguti",fullName:"Natalia Angelo Da Silva Miyaguti"},{id:"243768",title:"B.Sc.",name:"Sarah Christine",surname:"Pereira De Oliveira",slug:"sarah-christine-pereira-de-oliveira",fullName:"Sarah Christine Pereira De Oliveira"}],corrections:null},{id:"62824",title:"Adipose Tissue Remodeling during Cancer Cachexia",doi:"10.5772/intechopen.79979",slug:"adipose-tissue-remodeling-during-cancer-cachexia",totalDownloads:1094,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:1,abstract:"Cancer-induced cachexia (CC), characterized by systemic inflammation, body weight loss, adipose tissue (AT) remodeling, and muscle wasting, is a malignant metabolic syndrome with an undefined etiology. There is a consensus that multiple factors contribute to cancer-induced AT remodeling, and longitudinal studies show that patients lose AT before they start losing muscle mass. In CC, AT remodeling occurs predominantly through adipocyte atrophy, impairment of fatty acid turnover, inflammation, rearrangement of extracellular matrix (ECM), and browning of AT. More recently, some studies have shown that AT is affected early in the course of cachexia. Additionally, studies using experimental models have consistently indicated that the alterations in adipocyte metabolism begin quite early, followed by the downregulation of adipogenic and thermogenic genes. These sets of changes, in addition to metabolites derived from this process, maybe the initial (sterile) trigger of the sequence of events that result in the remodeling and dysfunction of AT in cachexia. Therefore, the present chapter aims to describe state of the art related to the subject of interest by analyzing the primary studies that have addressed the possible interface between inflammation and morphofunctional alterations of AT, in addition to the possible repercussions of this process during the development of CC.",signatures:"Miguel Luiz Batista Júnior and Felipe Henriques",downloadPdfUrl:"/chapter/pdf-download/62824",previewPdfUrl:"/chapter/pdf-preview/62824",authors:[{id:"242418",title:"Dr.",name:"Miguel Luiz",surname:"Batista Júnior",slug:"miguel-luiz-batista-junior",fullName:"Miguel Luiz Batista Júnior"},{id:"297029",title:"Dr.",name:"Felipe",surname:"Henriques",slug:"felipe-henriques",fullName:"Felipe Henriques"}],corrections:null},{id:"70415",title:"Current Approaches in Immunoassay Methods Focus on Skeletal Muscle Proteins",doi:"10.5772/intechopen.90629",slug:"current-approaches-in-immunoassay-methods-focus-on-skeletal-muscle-proteins",totalDownloads:737,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"The skeletal muscle is a complex tissue that represents most of the muscle tissue in mammals and plays a key role in health and in the body’s function. It is a heterogeneous tissue whose contractile and metabolic functions depend on type, size, and quality of a large number of proteins. The multitude of proteins, the relationships that exist between them, and functional changes that occur in different muscle pathologies make their investigation to be challenged. In this chapter, current approaches in proteomic studies, its application, specific technical advice, and recent progress of the most important techniques based on antigen-antibody interactions used for the analysis of muscle proteins involved in different muscle diseases are presented.",signatures:"Gisela Gaina",downloadPdfUrl:"/chapter/pdf-download/70415",previewPdfUrl:"/chapter/pdf-preview/70415",authors:[{id:"242747",title:"Dr.",name:"Gisela",surname:"Gaina",slug:"gisela-gaina",fullName:"Gisela Gaina"}],corrections:null}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"},subseries:null,tags:null},relatedBooks:[{type:"book",id:"6658",title:"Stromal Cells",subtitle:"Structure, Function, and Therapeutic Implications",isOpenForSubmission:!1,hash:"c215f02d4268e4b7cccdaea141ec8647",slug:"stromal-cells-structure-function-and-therapeutic-implications",bookSignature:"Mani T. 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Plant biomass production is strongly correlated with nitrogen (N) availability which, in most farming systems, is dependent on the use of N-fertilizers. These N-fertilizers are obtained, with few exceptions, from the Haber-Bosch industrial process of atmospheric N2 fixation which is energy demanding and responsible for 1.44% of the global emissions of carbon dioxide (CO2) [1]. Contrastingly, most plants of the family Fabaceae (legumes), which comprises 751 genera and 19,500 species [2], can establish symbiotic relationships with rhizobia bacteria capable of fixing atmospheric N2 into ammonia (NH3), through the development of root nodules that host the bacteria (bacteroids). This symbiosis has been explored by humankind since the early beginning of agriculture and it still is an essential part of many traditional agriculture farming systems (e.g., see [3]). In the Mediterranean basin and Europe at large, the rise of modern agriculture, which cannot be decoupled from relatively cheap N-fertilizers, has driven the abandonment of legumes in the farming systems. Still, legume usage in the frame of mixed pastures, and forages, did not decline over time as steeply as grain legumes did [4].
The Montado (in Portugal) or Dehesa (in Spain), is an agro-silvopastoral system, typical of the Southwestern part of the Iberian Peninsula, characterized by a savannah-like landscape, where the main tree species are cork and holm oak (
The biological N-fixation produced by the legume-rhizobia symbiosis may have a profound effect on the Montado/Dehesa ecosystem by increasing the N content of the system and its availability to grasses and other forbs, increasing the overall biomass production and the soil organic matter (SOM) content. The term rhizobia designate diazotrophic bacteria of two different classes of Proteobacteria, encompassing species and strains well beyond those of the genus
Increasing SOM content may help to counteract soil acidification, to the extent that SOM constitutes an important proton buffer, and SOM depletion and low calcium (Ca2+) saturation of the cation-exchange capacity (CEC) of the soil [13] may constitute one of the main reasons for soil acidification in the Montado/Dehesa system. The high concentration of protons in the soil solution leads to the solubilization of heavy metals that may become toxic to the plants, namely, aluminum (Al3+) and Mn2+ (e.g. [14, 15]). The concentration of these toxic elements that plants may endure will vary with species and cultivars but often they have much lower thresholds than their wild counterparts (e.g., [16]). In low pH soils, nodule formation and nodule weight can be reduced by percentages above 90% and 50%, respectively [17]. Rhizobia bacteria can be found in a wide range of proton concentrations, with species (strains) surviving at pH values as low as 4 [18]. Nonetheless, soil acidification might have a profound effect on the survival of the bacterial strains present and thus on the occurrence of matching symbionts [19].
Proton [H+] concentration in soil solution and the interaction with other elements, namely Al3+ and Mn2+, affect plant growth. Aluminum [Al3+] has no known biological function (e.g., [20]) but it can impair plant growth when in relatively high concentrations in the soil solution. The major factor affecting Al3+ concentration in soil solution is proton concentration and the presence of other ions that react with the dissolving/precipitating surfaces [15], namely, SOM (e.g., [21]). pH values above 4.5–5.5 are considered as leading to the precipitation of Al3+which in relatively high concentrations affects root elongation and root hair formation likely due to the binding to the pectic matrix of the cell walls, substituting Ca, and hence cell wall thickening and rigidity (e.g., [22, 23]). The aerial part of the plant is also affected by Al3+ via induced nutrient deficiencies of magnesium (Mg), Ca and P, phytohormones imbalances and drought stress [22], but transport to the shoots, with some exceptions, is usually limited [24]. Plant Al-tolerance is characterized by the production of root exudates, organic acids and mucilage capable to chelate Al3+, and by a lower CEC of the surface cell walls [22]. Pasture/forage legumes have different tolerance to different Al3+ concentrations. For example, the genus
Phosphorus [P] is an important element in molecules participating in the intracellular buffering system (the conjugate acid-base pair H2PO4−–HPO42−), in the energy metabolism of the cells (e.g., ATP, adenosine triphosphate), in the formation of nucleic acids, among others. In acidic soils, low available P in soil solution is mainly due to its retention as adsorbed P on the surface of soil particles of Al- and Fe oxides [37]. Some plant species can exudate to the rhizosphere important amounts of carboxylates that are capable to mobilize Al- and Fe-oxide-sorbed P and also organic P. The organic P is then hydrolyzed by phosphatases, which are exudate to the rhizosphere. The inorganic P uptake by the plant occurs through a high-affinity inorganic P transporter in the plasma membrane of the root cells, belonging to the PHT1 gene family [38]. This strategy of P-mobilization is accompanied by the mobilization of other nutrients such as Mn [29]. Another strategy most plants follow is the promotion of symbiosis with arbuscular mycorrhizal (AM) fungi capable of scavenging phosphorus (available P) [39]; this strategy will be discussed further ahead. The relative importance of each of these strategies of P uptake, for each plant species/cultivar, and the interactions with the environment, may have an impact on the availability of other nutrients, namely, Mn and their uptake. Plants must possess adequate levels of phosphorus (P) otherwise the N-fixation rate by the microsymbiont will be conditioned by P-availability. For example, the molybdenum-dependent nitrogenase requires for each mol of N2 reduction, 16 mol of ATP [40]. Nodulating plants allocate a substantial part of the P uptake to the nodules in soils with low available P [41] and P fertilization may have an important effect on biologically-fixated N (e.g. [42]).
Iron [Fe2+] is essential for biological N-fixation, for example, due to its role in the FeMo cofactor of nitrogenase [43] and the prosthetic group of the leghemoglobin. Fe content and availability to plants in acidic soils are usually high, but plant Fe-deficiency can occur in sandy soils with high concentrations of Mn2+ in soil solution [44]. Legumes, like all dicots, mobilize Fe through the acidification of the rhizosphere; the mobilized Fe3+is then reduced to Fe2+ by plasma membrane reductases and the uptake happens through plasma membrane iron-regulated transporters (IRT1), in what is known as the strategy I of iron uptake [45]. Mn and Fe antagonistic relationship has been observed in many studies with legumes and non-legumes (e.g. [46]). Izaguirre-Mayoral and Sinclair [34] observed that: (i) a higher Mn concentration in the leaves of two soybean cultivars when in the presence of low Fe and high Mn concentrations in the culture solution and; (ii) a lower concentration of Fe in the leaves with increasing Mn concentrations in the culture solutions with high Fe concentration. In acidic soils, the Mn-induced accumulation of Fe in the roots may affect nodulation and nitrogenase activity.
Calcium [Ca2+] is an essential nutrient in plant cells, namely, by its structural role in the cell walls and membranes, and the signaling role in the cytosol [47]. Calcium also plays many roles in the nodulation process of legumes, viz., in the root hair deformation and entrapment of rhizobia soon after nod factor release by the rhizobia [48]. The uptake of Ca2+ is mediated by plasma membrane transporters, the Ca channels [47]. These Ca channels may be permeable to Mn [28]. Nitrogenase activity can be reduced in acidic soils, particularly, if Ca concentration is low and at the early stages of plant development in common bean (
Magnesium [Mg2+], besides its role in the chlorophyll molecule, and in a multitude of enzymes, also plays an essential role in ATP; ATP, to become biologically active requires binding with Mg (e.g., [51]). Several studies show a negative effect of K on Mg concentration in the shoot tissues (for reviews see, e.g., [52, 53]. This interaction of K x Mg may be of significance because, in the acidic soils of the Montado/Dehesa, K availability might be high, and low Mg concentration in the plant shoots may have a significant effect on plant growth and nutritional value as feed. The Mg2+ transporter(s) responsible for uptake into the root cells is(are) poorly known (e.g., [52]), although there is evidence of Mg2+ transport through Ca-channels [47]. Reduced translocation of Mg from the roots to the shoots, in presence of high K+ concentration, might be the cause [53]. According to an analysis performed by Rietra et al. [52] on 94 peer-reviewed papers and 117 interactions (synergistic, antagonistic or zero-interactions) on crop yields, no interactions were found between Mg and Mn.
Molybdenum [Mo] is essential for some enzymes found in plants, involved in nitrogen metabolism and phytohormones synthesis [54]. Mo, as seen for Fe, is essential for biological N-fixation due to its role in the FeMo cofactor of nitrogenase [43]. A molybdate transporter type 1 (MTR1), that is a molybdate-specific transporter, has been identified in
In the Montado/Dehesa, biomass accretion happens from fall through winter and spring. The length of the growing period will vary as there is no consistent rainfall pattern from year to year. The daily minimum soil temperatures in the Winter months are often well below 5°C at 2 cm depth (e.g., [57]). In mid-Winter, as the growth rate of legumes increases in responding to favorable temperature and water availability so increases the potential for biological N-fixation. Biomass accretion of the annual species of the understorey ends in late May or early June after soil-available water has been used and the air temperatures are still relatively mild.
The tolerance of rhizobia to low temperatures varies, with different minimum temperatures for growth as low as 5°C, and survival −10°C [58]. Gibson [59] studied the effect of time and temperature in nodule formation of four subterranean clovers (
Extended periods of low or no precipitation during the growing season are very common in the Montado/Dehesa region and can affect symbiosis. Unsaturated soil conditions, and soil texture (especially in clayey soils), conditioning the diameter and continuity of saturated soil pores, affect rhizobia motility [62]. Thus, in the presence of a low concentration of rhizobia per gram of soil, the initiation of symbiosis may be dependent on transient saturated conditions after rainfall. N-fixation of nodulated legumes may be severely impaired by drought, well before photosynthesis is reduced, and the mechanisms for this response are species-specific and not fully understood; O2 limitation, C availability and N feedback mechanisms have been proposed as playing an important role in the regulation of nitrogenase activity during drought periods [63]. A better understanding of these mechanisms would allow faster and smarter breeding for drought-tolerant legume species. On the other hand, the Montado/Dehesa systems are located in peneplains, and waterlogging is a common problem in some areas. Waterlogging has a profound effect on aeration and the redox conditions of the soil that can impose high Mn2+ availability over time [14]. The nodules, in saturated soils, will be deprived of free O2, essential for the oxidation of the carbohydrates to produce the energy needed for the nitrogenase activity; also the diffusion of CO2 and H2, gases that can inhibit nitrogenase activity, will be hindered [61]. Roberts et al. [64] discuss the model/role of a gas diffusion barrier in the nodules, capable to maintain a microaerobic state, ca. 20 nM O2, under normal atmospheric conditions, that assure nitrogenase activity at suboptimal rates; changes of the O2 partial pressure of the atmosphere lead to short term changes of the gas diffusion barrier permeability and the rapid inhibition of the nitrogenase activity (transient and fully recoverable), or long term changes, leading to changes in the cellular and subcellular morphology, including the formation of lenticels and secondary aerenchyma on the surface of the nodules. Depending on the severity of the hypoxic conditions and the exposure time, the adaptation of the legume, regarding the number of nodules and nitrogenase activity, may not be sufficient and, depending on the species/cultivars, the recovery and survival might be compromised. Pampana et al. [65] observed that 5 days of waterlogging during the flowering period were sufficient to reduce the number of pods and seeds of white lupin plants almost three-fold, as well as seed weight and shoot and root dry matter. On the other range of the spectrum, Pugh et al. [66] observed that white clover (
Legumes, besides symbioses with rhizobia bacteria, can establish symbioses with AM fungi in mutualistic relationships where the fungi increase the plant uptake of water and nutrients, in particular phosphorus, and receive photosynthates in exchange [39]. Most plants are co-colonized by multiple AM fungi species and endemic AM fungi, well adapted to the soil conditions, will compete with inoculated AM fungi for mycorrhization of the roots [39]. These symbioses may be important for N-fixation if in the presence of low concentrations of plant-available P. The mycorrhizal component may account for much of the P uptake of legumes and the direct uptake can be residual. Nazeri et al. [33] showed that mycorrhizal plants of
To increase the soil productivity in the Montado/Dehesa ecosystem, the correction of the soil reaction by liming is expensive but, where economically viable, it is effective, either with calcitic or dolomitic limes (e.g., [13]). However, the economic and social benefits of liming must be balanced with the ecological impact of this practice. From an ecological point of view, liming contributes to the emissions of greenhouse gases (GHG) from mining, transporting and incorporating the lime into the soil. Additionally, liming causes a marked stratification of the soil profile pH and the effects on the forest stand and acidophilic endemic species, in the long term, are unknown. On the other hand, liming potentially yield higher carbon sequestration (SOM), the improvement of several topsoil properties, higher feed production and quality (protein content), just to name a few. Unfortunately, although there are many metric approaches to quantify these variables there is no reliable model to assist in the decision to correct the soil reaction through liming in the Montado/Dehesa.
Alternatively, and although in a wider time frame, the benefits of liming can be achieved through higher SOM content (increasing CEC and the soil buffering capacity) and the management of soil fertility and plant nutritional deficiencies. Endemic legumes species, with cultivars selected for the traits of interest, can increase the N content of the system and N availability to other forbs and grasses, and, along with the correction of plant nutrient deficiencies, enhance biomass production and SOM content. Seeding with no-till systems would allow the preservation of the SOM content, without the exacerbation of microbial activity. It would also allow a sequential introduction of the cultivars of interest, beginning with those species/cultivars that can tolerate the soil conditions and boost soil organic matter (cultivars selected aiming acid soils reclamation and tolerant to the low light conditions of the understorey), creating favorable conditions for the survival of the rhizobia of interest (already present or inoculated) and the preservation of AM fungi, in what can be defined as the first step in a
Pastures sowed with mixtures of legumes in the Montado/Dehesa, in soils with pH in water between 4.9 and 5.94, increased the biomass production by more than three-fold, as well as the SOM content, and the protein content of grasses and non-legume forbs [69]. However, the positive effects observed in this study decreased continually from the first year onwards, suggesting the inadequacy of the cultivars sowed. From a stepwise legume-enrichment perspective, lupins may play an important role in the first steps of legume enrichment. The Mediterranean basin is the place of origin of important annual lupin species, with an important genetic pool for plant breeders. For example, in 2009, the number of accessions (landrace and wild types) distributed among different institutions totalled 1804 in Portugal and 5057 in Spain [70]. Lupins are tolerant to acidic soils, with low available P, and can cope with very high concentrations of Mn in the shoot tissues (e.g. [71]). Thus, at least conceptually, well-adapted cultivars of lupins, with good biomass accretion, mixed with other highly tolerant hardy cultivars of other genera could be sowed, increasing SOM and nutrient availability, and establishing/increasing the microsymbionts population, and their ability to survive. In this respect, lupins do not possess very high specificity to their rhizobia microsymbiont, being able to establish symbiosis with several species of
The potential for biological N-fixation with legumes in the Montado/Dehesa systems is lower than in more northern regions in Europe due to the erratic rainfall patterns and the relatively low temperature during part of the growing season, and the poor and strongly acid soils. Increasing the potential N-fixation through liming is expensive and, in these sensitive biodiverse systems, with unknown consequences in the long term.
Legumes bred for tolerance to acid soils and associated metal toxicity, for drought and waterlogging, and for the low light conditions in Winter, could provide biodiversity and the potential to increase N-fixation in the multi-diverse environment, both spatial and temporal, of the Montado/Dehesa. A
The avenues of research that are needed may prove beneficial beyond the natural borders of the Montado/Dehesa, by identifying legume cultivars and rhizobia strains tolerant to strongly acidic soil conditions useful in other regions of the world.
The author declares no conflict of interest.
This work is funded by National Funds through FCT - Foundation for Science and Technology under the Project UIDB/05183/2020.
Optical chromatography (OC) is an increasingly adapted technique for label-free sorting and analysis of bioparticles including cells, bacteria, fungi [1, 2, 3, 4]. It exploits a lightly focused Gaussian laser beam within a microfluidic channel to create opposing optical scattering and fluidic drag forces. One can leverage these controllable forces to realize selective fractionation of bioparticles in a heterogeneous mixture based on size, morphology or chemical composition (i.e., refractive index variation) [5, 6]. OC technique was first implemented in size-based fractionation of inorganic materials such as polystyrene beads. Later, researchers employed this technique for size-based fractionation and sorting of organic particles including human blood constituents including erythrocytes, monocytes, granulocytes, and lymphocytes [2, 5]. Subsequently, differentiation of micronscale bioparticles with subtle differences [4, 7], including those with size differences as small as 70 nm [8], are shown. In addition to size-based separation, OC technique also offers refractive index-based fractionation capability, allowing separation of bioparticles with minuscule differences in chemical composition, such as
In a recent publication, we introduced a novel plasmonic nanopore device that eliminates the shortcomings of the conventional OC technique [11]. Here, we review this hybrid Optofluidic PlasmonIC (OPtIC) device merging light focusing and fluidic flow through a tiny (4 μm × 4 μm footprint) plasmonic microlens housing an integrated nanopore channel. Based on a subwavelength-thick (∼ 200 nm) suspended device structure, our optofluidic approach opens the door to practical, scalable, and high-throughput on-chip particle sorting.
In Figure 1a, an OPtIC device that consists of a periodic nanohole array (NHA) defined in a suspended multilayer membrane is shown. The mechanically robust membrane consists of a free-standing 100 nm thick silicon nitride (Si3N4) substrate coated with 100 nm thick gold (Au) and a 5 nm thick titanium (Ti) adhesion layer. The total thickness of the microlens is
OPtIC nanopore device enabling selective sorting of bioparticles: (a) top view of OPtIC microlens consisting of a 9 × 9 NHA with enlarged central aperture. (b) Nanofluidic flow pattern across the OPtIC device with 1.3 μm/s flow rate at the focal point. (c) Conceptual illustration of the selective separation mechanism for nano-bioparticles through counter acting forces at the focal point. Copyright 2020 nature publishing group adapted with permission [
Figure 1b depicts the cross-sectional view of nanofluidic flow pattern across the OPtIC device calculated using steady-state finite-element method (FEM) simulations (COMSOL Multiphysics). The overall size of the computational domain in Figure 1b is 50 μm × 50 μm × 40 μm. The inlet fluidic flow is directed towards the central aperture, where flow velocity is largest along the optical (
A close-up cross-sectional view of the OPtIC device is given in Figure 1c, where the fluidic flow is in the -
Figure 1c depicts that large particles with diameters above a threshold are driven against the fluid flow (i.e. in the +
Optical radiation force acting on nano-bioparticles can be divided into scattering
where
where
with
The central nanopore opening plays a key role in precise alignment of fluidic flow along the optical axis and determining the threshold rejection diameter. On the electromagnetic part, it also controls the focusing characteristics of the OPtIC microlens. Hence, it should be ensured that the focusing behavior does not deteriorate for an admissible
Monochromatic light focusing behavior with varying central nanopore dimensions: (a) focusing behavior of OPtIC microlens for
The dashed horizontal lines in Figure 2a, corresponding to focal point, indicate that the focal length (
The light focusing mechanism of OPtIC microlens relies on the periodic arrangement of smaller nanoholes around the central one. The EOT effect occurs when the Bragg condition is met, i.e.,
An important observation in Figure 2a is the checkerboard-like pattern just above the OPtIC microlens surface, which arises from plasmonic Talbot effect, that is diffractive self-imaging of smaller-diameter nanoholes [13, 26]. On the other hand, intensity right over the central aperture is significantly enhanced for
Light focusing behavior due to in-phase interactions: Near-field phase maps of the hot intensity spots around the OPtIC nanopore device are presented for varying
Light intensity around the central nanopore opening increases with increasing
In the preceding section, we showed that the OPtIC nanopore device can focus collimated monochromatic light at
Broadband light focusing: (a) simulated light focusing behavior of the optimized OPtIC microlens with
Optical intensity variation along the focal plane (dashed lines in Figure 4a) is shown in Figure 4b. Focal point has a FWHM of 1.08 μm, 1.12 μm, 1.24 μm and 1.28 μm at
Using the Rayleigh-Sommerfeld (R-S) formula [13, 28, 29], the focal length of the finite-size NHA microlens can be calculated:
where
As conventional wisdom suggests, surface plasmon generation is accompanied by electromagnetic heating, which evokes heat-induced fluid dynamics. The local temperature elevation in the vicinity of the OPtIC microlens induces a buoyance-driven convective fluid flow (Archimedes force) against the reverse main flow stream, resulting in a thermo-plasmonic drag force that drives particles away from the microlens surface [30, 31]. A comprehensive review of this physical mechanism – thermo-induced fluid motion - can be found elsewhere [32, 33]. In this work, thermo-plasmonic drag forces are calculated using Multiphysics FEM simulations, which incorporate electromagnetic (EM) wave, heat transfer and Navier–Stokes equations. Here, we solve the EM wave Equation [34].
where
where
and Stoke’s equation
where
Steady-state 2D temperature spatial distributions in the
Thermo-plasmonic heating and Rayleigh–Bénard flow: (a) temperature distribution on the OPtIC nanopore device surface under illumination (633 nm wavelength and 20 mW total power). (b) Temperature distribution and heat-induced fluidic flow pattern on a perpendicular plane crossing the optical axis. The arrows represent the velocity vector
OPtIC nanopore device enables both size- and refractive-index based separation of nano-bioparticles by utilizing a delicate balance of counteracting forces, i.e.,
Label-free selective sorting of nanoparticles:
Size-based separation is not adequate when similar size bioparticles of different origins need to be separated. As indicated in Eq. (1), the optical radiation force acting on particles is a function of both particle radius and refractive index. In this respect, particles comparable dimensions can be separated based on their refractive indices [4, 7]. In general, refractive index is intimately linked to the internal structure and chemical makeup of the nano-bioparticles [e.g., exosomes, viruses]. A recent research study has shown that implementation of optical chromatography based on refractive index differences yield successful differentiation of cells with single gene modifications [3]. We calculated forces (
It is known that exosomes (nanovesicles composed mostly of water enclosed by a thin phospholipid membrane) have lower refractive indices
The threshold
A major limitation of conventional OC is the difficulty of aligning fluidic flow against a lightly focused Gaussian beam in a precise manner [6]. Our OPtIC nanopore device employs a self-collimation mechanism effortlessly aligning fluidic flow along the optical axis of the microlens. This self-collimation capability, lining-up particles against the scattering force, is demonstrated in Figure 7. We calculated radial components of the optical gradient (
Self-collimating radial forces along the optical axis: The radial components of
As shown in Figure 7, nanoparticles in the focal are mainly retained along the optical axis by the optical gradient force
In this chapter, we reviewed a facile optofluidic nanopore platform for the purposes of optical chromatography of nano-bioparticles based on their size and/or refractive index (chemical composition). Consisting of a finite-size periodic plasmonic nanohole array on a suspended membrane, this OPtIC nanopore device with an enlarged central aperture facilitates precise alignment of optical scattering, thermo-plasmonic drag, and fluidic drag forces against each other for the purposes of OC. Its self-collimation mechanism eliminates the need for sophisticated and bulky optic components (e.g., lasers, microscope objectives, multi-axis stages, etc.) that are commonly used in conventional OC techniques. Furthermore, our plasmonic microlens opens the door to use of incoherent light source, such as LEDs, for the purposes of OC by readily focusing collimated broadband light into a tight spot. This lensing mechanism provides a robust separation capability that is insensitive to structural variations of the central nanopore. We demonstrated size-based selective sorting of nano-bioparticles, such as exosomes, with a tunable threshold diameter using incident light power or fluidic flow rate. In addition, refractive-index based separation of identical size nano-bioparticles are shown. Similar to size-based separation, the refractive-index (material composition) based separation mechanism is readily tunable through incident light power and fluidic flow rate.
A. A. Yanik acknowledges support from National Science Foundation [ECCS-1611290], Gordon and Betty Moore Foundation [GBMF #5263.06], and National Science Foundation CAREER Award [ECCS- 1847733]. X. Zhu was supported by a University of California Chancellor’s Dissertation Year Fellowship. We acknowledge Dr. Tom Yuzvinsky for assistance with device fabrication and the W.M. Keck Center for Nanoscale Optofluidics for use of the FEI Quanta 3D.
The authors declare no conflict of interest.
"Open access contributes to scientific excellence and integrity. It opens up research results to wider analysis. It allows research results to be reused for new discoveries. And it enables the multi-disciplinary research that is needed to solve global 21st century problems. Open access connects science with society. It allows the public to engage with research. To go behind the headlines. And look at the scientific evidence. And it enables policy makers to draw on innovative solutions to societal challenges".
\n\nCarlos Moedas, the European Commissioner for Research Science and Innovation at the STM Annual Frankfurt Conference, October 2016.
",metaTitle:"About Open Access",metaDescription:"Open access contributes to scientific excellence and integrity. It opens up research results to wider analysis. It allows research results to be reused for new discoveries. And it enables the multi-disciplinary research that is needed to solve global 21st century problems. Open access connects science with society. It allows the public to engage with research. To go behind the headlines. And look at the scientific evidence. And it enables policy makers to draw on innovative solutions to societal challenges.\n\nCarlos Moedas, the European Commissioner for Research Science and Innovation at the STM Annual Frankfurt Conference, October 2016.",metaKeywords:null,canonicalURL:"about-open-access",contentRaw:'[{"type":"htmlEditorComponent","content":"The Open Access publishing movement started in the early 2000s when academic leaders from around the world participated in the formation of the Budapest Initiative. They developed recommendations for an Open Access publishing process, “which has worked for the past decade to provide the public with unrestricted, free access to scholarly research—much of which is publicly funded. Making the research publicly available to everyone—free of charge and without most copyright and licensing restrictions—will accelerate scientific research efforts and allow authors to reach a larger number of readers” (reference: http://www.budapestopenaccessinitiative.org)
\\n\\nIntechOpen’s co-founders, both scientists themselves, created the company while undertaking research in robotics at Vienna University. Their goal was to spread research freely “for scientists, by scientists’ to the rest of the world via the Open Access publishing model. The company soon became a signatory of the Budapest Initiative, which currently has more than 1000 supporting organizations worldwide, ranging from universities to funders.
\\n\\nAt IntechOpen today, we are still as committed to working with organizations and people who care about scientific discovery, to putting the academic needs of the scientific community first, and to providing an Open Access environment where scientists can maximize their contribution to scientific advancement. By opening up access to the world’s scientific research articles and book chapters, we aim to facilitate greater opportunity for collaboration, scientific discovery and progress. We subscribe wholeheartedly to the Open Access definition:
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\\n\\nLicense
\\n\\nBook chapters published in edited volumes are distributed under the Creative Commons Attribution 3.0 Unported License (CC BY 3.0). IntechOpen upholds a very flexible Copyright Policy. There is no copyright transfer to the publisher and Authors retain exclusive copyright to their work. All Monographs/Compacts are distributed under the Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0). Read more
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\\n\\nAll scientific works are Peer Reviewed prior to publishing. Read more
\\n\\nOA Publishing Fees
\\n\\nThe Open Access publishing model employed by IntechOpen eliminates subscription charges and pay-per-view fees, enabling readers to access research at no cost. In order to sustain operations and keep our publications freely accessible we levy an Open Access Publishing Fee for manuscripts, which helps us cover the costs of editorial work and the production of books. Read more
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\\n\\nIntechOpen is committed to ensuring the long-term preservation and the availability of all scholarly research we publish. We employ a variety of means to enable us to deliver on our commitments to the scientific community. Apart from preservation by the Croatian National Library (for publications prior to April 18, 2018) and the British Library (for publications after April 18, 2018), our entire catalogue is preserved in the CLOCKSS archive.
\\n\\nOpen Science is transparent and accessible knowledge that is shared and developed through collaborative networks.
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The Open Access publishing movement started in the early 2000s when academic leaders from around the world participated in the formation of the Budapest Initiative. They developed recommendations for an Open Access publishing process, “which has worked for the past decade to provide the public with unrestricted, free access to scholarly research—much of which is publicly funded. Making the research publicly available to everyone—free of charge and without most copyright and licensing restrictions—will accelerate scientific research efforts and allow authors to reach a larger number of readers” (reference: http://www.budapestopenaccessinitiative.org)
\n\nIntechOpen’s co-founders, both scientists themselves, created the company while undertaking research in robotics at Vienna University. Their goal was to spread research freely “for scientists, by scientists’ to the rest of the world via the Open Access publishing model. The company soon became a signatory of the Budapest Initiative, which currently has more than 1000 supporting organizations worldwide, ranging from universities to funders.
\n\nAt IntechOpen today, we are still as committed to working with organizations and people who care about scientific discovery, to putting the academic needs of the scientific community first, and to providing an Open Access environment where scientists can maximize their contribution to scientific advancement. By opening up access to the world’s scientific research articles and book chapters, we aim to facilitate greater opportunity for collaboration, scientific discovery and progress. We subscribe wholeheartedly to the Open Access definition:
\n\n“By “open access” to [peer-reviewed research literature], we mean its free availability on the public internet, permitting any users to read, download, copy, distribute, print, search, or link to the full texts of these articles, crawl them for indexing, pass them as data to software, or use them for any other lawful purpose, without financial, legal, or technical barriers other than those inseparable from gaining access to the internet itself. The only constraint on reproduction and distribution, and the only role for copyright in this domain, should be to give authors control over the integrity of their work and the right to be properly acknowledged and cited” (reference: http://www.budapestopenaccessinitiative.org)
\n\nOAI-PMH
\n\nAs a firm believer in the wider dissemination of knowledge, IntechOpen supports the Open Access Initiative Protocol for Metadata Harvesting (OAI-PMH Version 2.0). Read more
\n\nLicense
\n\nBook chapters published in edited volumes are distributed under the Creative Commons Attribution 3.0 Unported License (CC BY 3.0). IntechOpen upholds a very flexible Copyright Policy. There is no copyright transfer to the publisher and Authors retain exclusive copyright to their work. All Monographs/Compacts are distributed under the Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0). Read more
\n\nPeer Review Policies
\n\nAll scientific works are Peer Reviewed prior to publishing. Read more
\n\nOA Publishing Fees
\n\nThe Open Access publishing model employed by IntechOpen eliminates subscription charges and pay-per-view fees, enabling readers to access research at no cost. In order to sustain operations and keep our publications freely accessible we levy an Open Access Publishing Fee for manuscripts, which helps us cover the costs of editorial work and the production of books. Read more
\n\nDigital Archiving Policy
\n\nIntechOpen is committed to ensuring the long-term preservation and the availability of all scholarly research we publish. We employ a variety of means to enable us to deliver on our commitments to the scientific community. Apart from preservation by the Croatian National Library (for publications prior to April 18, 2018) and the British Library (for publications after April 18, 2018), our entire catalogue is preserved in the CLOCKSS archive.
\n\nOpen Science is transparent and accessible knowledge that is shared and developed through collaborative networks.
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\n\nWe aim at improving the quality and availability of scholarly communication by promoting and practicing:
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Cells encode “receptors” containing Ub-/Ubl-binding domains that interpret and translate each modification into appropriate cellular responses. Among the different Ubls, NEDD8, which is the ubiquitin’s closest relative, retains many of the structural determinants that enable ubiquitin the ability to target proteins to degradation. Nevertheless, the direct involvement of NEDD8 conjugation to proteasome recruitment has been proved only in a few cases. To date, well-defined major NEDD8 substrates are primarily members of the cullin family, and cullin neddylation does not appear to mark these proteins for degradation. Various studies have demonstrated that selectivity between ubiquitin and NEDD8 is guaranteed by small but substantial differences. Nevertheless, several issues still need to be addressed, mainly concerning which interaction surfaces mediate NEDD8 function and what domains recognize them. Recently, two novel domains identified in KHNYN and N4BP1 proteins have shed new light on this research area. Here, I discuss some recent reports that contributed to shed light on the mechanisms underlining the discrimination between ubiquitin and NEDD8. Understanding the details of these molecular mechanisms represents a prominent facet for the identification of new therapeutic targets.",book:{id:"8301",slug:"ubiquitin-proteasome-system-current-insights-into-mechanism-cellular-regulation-and-disease",title:"Ubiquitin Proteasome System",fullTitle:"Ubiquitin Proteasome System - Current Insights into Mechanism Cellular Regulation and Disease"},signatures:"Elena Santonico",authors:[{id:"271923",title:"Dr.",name:"Elena",middleName:null,surname:"Santonico",slug:"elena-santonico",fullName:"Elena Santonico"}]},{id:"28199",doi:"10.5772/31082",title:"F0F1 ATP Synthase: A Fascinating Challenge for Proteomics",slug:"f0f1-atp-synthase-a-fascinating-challenge-for-proteomics",totalDownloads:5574,totalCrossrefCites:2,totalDimensionsCites:8,abstract:null,book:{id:"780",slug:"proteomics-human-diseases-and-protein-functions",title:"Proteomics",fullTitle:"Proteomics - Human Diseases and Protein Functions"},signatures:"Federica Dabbeni-Sala, Amit Kumar Rai and Giovanna Lippe",authors:[{id:"85523",title:"Prof.",name:"Giovanna",middleName:null,surname:"Lippe",slug:"giovanna-lippe",fullName:"Giovanna Lippe"},{id:"149272",title:"Dr.",name:"Federica",middleName:null,surname:"Dabbeni-Sala",slug:"federica-dabbeni-sala",fullName:"Federica Dabbeni-Sala"},{id:"149273",title:"Dr.",name:"Amit",middleName:null,surname:"Kumar Rai",slug:"amit-kumar-rai",fullName:"Amit Kumar Rai"}]},{id:"65025",doi:"10.5772/intechopen.82883",title:"E3 Ubiquitin Ligases in Cancer and Their Pharmacological Targeting",slug:"e3-ubiquitin-ligases-in-cancer-and-their-pharmacological-targeting",totalDownloads:1693,totalCrossrefCites:2,totalDimensionsCites:8,abstract:"Ubiquitination plays many critical roles in protein function and regulation. Consequently, mutation and aberrant expression of E3 ubiquitin ligases can drive cancer progression. Identifying key ligase-substrate relationships is crucial to understanding the molecular basis and pathways behind cancer and toward identifying novel targets for cancer therapeutics. Here, we review the importance of E3 ligases in the regulating the hallmarks of cancer, discuss some of the key and novel E3 ubiquitin ligases that drive tumor formation and angiogenesis, and review the clinical development of inhibitors that antagonize their function. We conclude with perspectives on the field and future directions toward understanding ubiquitination and cancer progression.",book:{id:"8301",slug:"ubiquitin-proteasome-system-current-insights-into-mechanism-cellular-regulation-and-disease",title:"Ubiquitin Proteasome System",fullTitle:"Ubiquitin Proteasome System - Current Insights into Mechanism Cellular Regulation and Disease"},signatures:"Joseph Y. Ong and Jorge Z. Torres",authors:[{id:"186645",title:"Dr.",name:"Jorge",middleName:null,surname:"Torres",slug:"jorge-torres",fullName:"Jorge Torres"},{id:"264944",title:"Mr.",name:"Joseph",middleName:null,surname:"Ong",slug:"joseph-ong",fullName:"Joseph Ong"}]},{id:"28201",doi:"10.5772/31113",title:"Identification of the Novel Plasminogen Receptor, Plg-RKT",slug:"identification-of-the-novel-plasminogen-receptor-plg-rkt",totalDownloads:2452,totalCrossrefCites:1,totalDimensionsCites:5,abstract:null,book:{id:"780",slug:"proteomics-human-diseases-and-protein-functions",title:"Proteomics",fullTitle:"Proteomics - Human Diseases and Protein Functions"},signatures:"Lindsey A. Miles, Nicholas M. Andronicos, Emily I. Chen, Nagyung Baik, Hongdong Bai, Caitlin M. Parmer, Shahrzad Lighvani, Samir Nangia, William B. Kiosses, Mark P. Kamps, John R. Yates III and Robert J. Parmer",authors:[{id:"85634",title:"Dr.",name:"Lindsey A.",middleName:null,surname:"Miles",slug:"lindsey-a.-miles",fullName:"Lindsey A. 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Yates, III"},{id:"85781",title:"Dr.",name:"Robert J.",middleName:null,surname:"Parmer",slug:"robert-j.-parmer",fullName:"Robert J. Parmer"},{id:"123594",title:"Dr.",name:"Samir",middleName:null,surname:"Nangia",slug:"samir-nangia",fullName:"Samir Nangia"},{id:"123595",title:"Dr.",name:"Shahrzad",middleName:null,surname:"Lighvani",slug:"shahrzad-lighvani",fullName:"Shahrzad Lighvani"}]}],mostDownloadedChaptersLast30Days:[{id:"70577",title:"Proteoforms: General Concepts and Methodological Process for Identification",slug:"proteoforms-general-concepts-and-methodological-process-for-identification",totalDownloads:939,totalCrossrefCites:1,totalDimensionsCites:1,abstract:"The term proteoform is used to denote all the molecular forms in which the protein product of a single gene can be found. The most frequent processes that lead to transcript modification and the biological implications of these changes observed in the final protein product will be discussed. Proteoforms arising from genetic variations, alternatively spliced RNA transcripts and post-translational modifications will be commented. This chapter will present an evolution of the techniques used to identify the proteoforms and the importance of this identification for understanding of biological processes. This chapter highlights the fundamental concepts in the field of top-down mass spectrometry (TDMS), and provides numerous examples for the use of knowledge obtained from the identification of proteoforms. The identification of mutant proteins is one of the emerging areas of proteogenomics and has the potential to recognize novel disease biomarkers and may point to useful targets for identification of therapeutic approaches.",book:{id:"9352",slug:"proteoforms-concept-and-applications-in-medical-sciences",title:"Proteoforms",fullTitle:"Proteoforms - Concept and Applications in Medical Sciences"},signatures:"Jucélia da Silva Araújo and Olga Lima Tavares Machado",authors:[{id:"30130",title:"Dr.",name:"Olga Lima Tavares",middleName:null,surname:"Machado",slug:"olga-lima-tavares-machado",fullName:"Olga Lima Tavares Machado"},{id:"310148",title:"Dr.",name:"Jucelia",middleName:null,surname:"Da Silva Araujo",slug:"jucelia-da-silva-araujo",fullName:"Jucelia Da Silva Araujo"}]},{id:"65025",title:"E3 Ubiquitin Ligases in Cancer and Their Pharmacological Targeting",slug:"e3-ubiquitin-ligases-in-cancer-and-their-pharmacological-targeting",totalDownloads:1693,totalCrossrefCites:2,totalDimensionsCites:8,abstract:"Ubiquitination plays many critical roles in protein function and regulation. Consequently, mutation and aberrant expression of E3 ubiquitin ligases can drive cancer progression. Identifying key ligase-substrate relationships is crucial to understanding the molecular basis and pathways behind cancer and toward identifying novel targets for cancer therapeutics. Here, we review the importance of E3 ligases in the regulating the hallmarks of cancer, discuss some of the key and novel E3 ubiquitin ligases that drive tumor formation and angiogenesis, and review the clinical development of inhibitors that antagonize their function. We conclude with perspectives on the field and future directions toward understanding ubiquitination and cancer progression.",book:{id:"8301",slug:"ubiquitin-proteasome-system-current-insights-into-mechanism-cellular-regulation-and-disease",title:"Ubiquitin Proteasome System",fullTitle:"Ubiquitin Proteasome System - Current Insights into Mechanism Cellular Regulation and Disease"},signatures:"Joseph Y. Ong and Jorge Z. Torres",authors:[{id:"186645",title:"Dr.",name:"Jorge",middleName:null,surname:"Torres",slug:"jorge-torres",fullName:"Jorge Torres"},{id:"264944",title:"Mr.",name:"Joseph",middleName:null,surname:"Ong",slug:"joseph-ong",fullName:"Joseph Ong"}]},{id:"65109",title:"Ubiquitin Signaling in Regulation of the Start of the Cell Cycle",slug:"ubiquitin-signaling-in-regulation-of-the-start-of-the-cell-cycle",totalDownloads:1595,totalCrossrefCites:2,totalDimensionsCites:3,abstract:"The small protein ubiquitin plays a vital role in virtually all aspects of cellular life. Among the diverse signaling outcomes associated with ubiquitination, the most well-established is the targeted degradation of substrates via the proteasome. During cell growth and proliferation, ubiquitin plays an outsized role in promoting progression through the cell cycle. In particular, ubiquitin-mediated degradation is critically important at transition points where it provides directionality and irreversibility to the cell cycle, which is essential for maintaining genome integrity. Specifically, the boundary between G1 and S-phase is tightly regulated by the ubiquitin proteasome system. Notably, the G1/S boundary represents a major barrier to cell proliferation and is universally dysfunctional in cancer cells, allowing for the unbridled proliferation observed in malignancy. Numerous E3 ubiquitin ligases, which facilitate the ubiquitination of specific substrates, have been shown to control G1/S. In this chapter, we will discuss components in the ubiquitin proteasome system that are implicated in G1/S control, how these enzymes are interconnected, gaps in our current knowledge, and the potential role of these pathways in the cancer cycle and disease proliferation.",book:{id:"8301",slug:"ubiquitin-proteasome-system-current-insights-into-mechanism-cellular-regulation-and-disease",title:"Ubiquitin Proteasome System",fullTitle:"Ubiquitin Proteasome System - Current Insights into Mechanism Cellular Regulation and Disease"},signatures:"Michael James Emanuele and Taylor Paige Enrico",authors:[{id:"264977",title:"Dr.",name:"Michael",middleName:null,surname:"Emanuele",slug:"michael-emanuele",fullName:"Michael Emanuele"},{id:"282200",title:"Ms.",name:"Taylor",middleName:null,surname:"Enrico",slug:"taylor-enrico",fullName:"Taylor Enrico"}]},{id:"60432",title:"Protein-Based Detection Methods for Genetically Modified Crops",slug:"protein-based-detection-methods-for-genetically-modified-crops",totalDownloads:1463,totalCrossrefCites:3,totalDimensionsCites:4,abstract:"The generation of genetically modified (GM) crops is rapidly expanding each and every year around the world. The well-being and quality assessment of these harvests are vital issues with respect to buyers’ interests. This drove the administrative specialists to execute an arrangement of extremely strict strategies for the endorsement to develop and use GMOs and to produce an interest in scientific techniques equipped for identifying GM crops. The GM crops have been added to the effective fuse of various attributes by presenting transgenes, for example, Bacillus thuringiensis (Bt) insecticidal qualities, in various crop species. GM crops give critical financial, natural, well-being and social advantages to both small and large agriculturists. The detection strategies incorporate either DNA-based or protein-based measures. Different immunoassays or catalyst connected immunosorbent tests are delicate and more affordable; however, they need experienced technicians. A very simple method, that is, immunochromatographic (ICS) test, is set up in the world, which is modest, compact and simple to utilize. The ICS is a semiquantitative method for indicative screening and semi-measurement of new remote proteins presented through hereditary change of plants. 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He is currently a principal researcher in data analytics and optimisation at TECNALIA (Spain), a visiting fellow at the Basque Center for Applied Mathematics (BCAM) and a part-time lecturer at the University of the Basque Country (UPV/EHU). His research interests gravitate on the use of descriptive, prescriptive and predictive algorithms for data mining and optimization in a diverse range of application fields such as Energy, Transport, Telecommunications, Health and Industry, among others. In these fields he has published more than 240 articles, co-supervised 8 Ph.D. theses, edited 6 books, coauthored 7 patents and participated/led more than 40 research projects. 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He is currently a full professor in\nthe Department of Automation and Applied Informatics at the\nsame university. Dr. Voloşencu is the author of ten books, seven\nbook chapters, and more than 160 papers published in journals\nand conference proceedings. He has also edited twelve books and\nhas twenty-seven patents to his name. He is a manager of research grants, editor in\nchief and member of international journal editorial boards, a former plenary speaker, a member of scientific committees, and chair at international conferences. His\nresearch is in the fields of control systems, control of electric drives, fuzzy control\nsystems, neural network applications, fault detection and diagnosis, sensor network\napplications, monitoring of distributed parameter systems, and power ultrasound\napplications. 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