Available data for diesel hybrid bus fuel economy in London. The values for l/100 km have been converted from miles per gallon using Litres100 km = (100*4.54609)/(1.609344*mpguk).
\\n\\n
Dr. Pletser’s experience includes 30 years of working with the European Space Agency as a Senior Physicist/Engineer and coordinating their parabolic flight campaigns, and he is the Guinness World Record holder for the most number of aircraft flown (12) in parabolas, personally logging more than 7,300 parabolas.
\\n\\nSeeing the 5,000th book published makes us at the same time proud, happy, humble, and grateful. This is a great opportunity to stop and celebrate what we have done so far, but is also an opportunity to engage even more, grow, and succeed. It wouldn't be possible to get here without the synergy of team members’ hard work and authors and editors who devote time and their expertise into Open Access book publishing with us.
\\n\\nOver these years, we have gone from pioneering the scientific Open Access book publishing field to being the world’s largest Open Access book publisher. Nonetheless, our vision has remained the same: to meet the challenges of making relevant knowledge available to the worldwide community under the Open Access model.
\\n\\nWe are excited about the present, and we look forward to sharing many more successes in the future.
\\n\\nThank you all for being part of the journey. 5,000 times thank you!
\\n\\nNow with 5,000 titles available Open Access, which one will you read next?
\\n\\nRead, share and download for free: https://www.intechopen.com/books
\\n\\n\\n\\n
\\n"}]',published:!0,mainMedia:null},components:[{type:"htmlEditorComponent",content:'
Preparation of Space Experiments edited by international leading expert Dr. Vladimir Pletser, Director of Space Training Operations at Blue Abyss is the 5,000th Open Access book published by IntechOpen and our milestone publication!
\n\n"This book presents some of the current trends in space microgravity research. The eleven chapters introduce various facets of space research in physical sciences, human physiology and technology developed using the microgravity environment not only to improve our fundamental understanding in these domains but also to adapt this new knowledge for application on earth." says the editor. Listen what else Dr. Pletser has to say...
\n\n\n\nDr. Pletser’s experience includes 30 years of working with the European Space Agency as a Senior Physicist/Engineer and coordinating their parabolic flight campaigns, and he is the Guinness World Record holder for the most number of aircraft flown (12) in parabolas, personally logging more than 7,300 parabolas.
\n\nSeeing the 5,000th book published makes us at the same time proud, happy, humble, and grateful. This is a great opportunity to stop and celebrate what we have done so far, but is also an opportunity to engage even more, grow, and succeed. It wouldn't be possible to get here without the synergy of team members’ hard work and authors and editors who devote time and their expertise into Open Access book publishing with us.
\n\nOver these years, we have gone from pioneering the scientific Open Access book publishing field to being the world’s largest Open Access book publisher. Nonetheless, our vision has remained the same: to meet the challenges of making relevant knowledge available to the worldwide community under the Open Access model.
\n\nWe are excited about the present, and we look forward to sharing many more successes in the future.
\n\nThank you all for being part of the journey. 5,000 times thank you!
\n\nNow with 5,000 titles available Open Access, which one will you read next?
\n\nRead, share and download for free: https://www.intechopen.com/books
\n\n\n\n
\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:"9246",leadTitle:null,fullTitle:"Satellites Missions and Technologies for Geosciences",title:"Satellites Missions and Technologies for Geosciences",subtitle:null,reviewType:"peer-reviewed",abstract:"Being a vital modern technology, satellite systems for navigation, telecommunication, and geosciences have developed rapidly in the last 25 years. Modern satellite technologies have become a base of our civilization and support our day-to-day activity in both practice and geosciences. This book is devoted to GNSS-remote sensing for ionosphere research, modeling and mitigation techniques to diminish the ionosphere and multipath impacts on GNSS, and survey of the modern satellite missions and technologies. We hope that the experts’ opinions presented in the book will be interesting for the research community and students in the area of satellites and space missions as well as in engineering and geoscience research.",isbn:"978-1-78985-996-6",printIsbn:"978-1-78985-995-9",pdfIsbn:"978-1-78985-301-8",doi:"10.5772/intechopen.83246",price:119,priceEur:129,priceUsd:155,slug:"satellites-missions-and-technologies-for-geosciences",numberOfPages:182,isOpenForSubmission:!1,isInWos:null,isInBkci:!1,hash:"f23d04613b089dae40f81342c3e7c7f4",bookSignature:"Vladislav Demyanov and Jonathan Becedas",publishedDate:"July 22nd 2020",coverURL:"https://cdn.intechopen.com/books/images_new/9246.jpg",numberOfDownloads:7985,numberOfWosCitations:8,numberOfCrossrefCitations:28,numberOfCrossrefCitationsByBook:0,numberOfDimensionsCitations:46,numberOfDimensionsCitationsByBook:0,hasAltmetrics:1,numberOfTotalCitations:82,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"March 19th 2019",dateEndSecondStepPublish:"September 23rd 2019",dateEndThirdStepPublish:"November 22nd 2019",dateEndFourthStepPublish:"February 10th 2020",dateEndFifthStepPublish:"April 10th 2020",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6,7",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"154597",title:"Prof.",name:"Vladislav",middleName:null,surname:"Demyanov",slug:"vladislav-demyanov",fullName:"Vladislav Demyanov",profilePictureURL:"https://mts.intechopen.com/storage/users/154597/images/system/154597.jpeg",biography:"Professor Vladislav Demyanov graduated from Irkutsk Military Aviation Engineering Institute as an electronic engineer in 1993, received his PhD in radio-wave physics from Irkutsk State University in 2000 and his doctorate of science degree in Engineering from Siberian Federal University (Krasnoyarsk, Russia) in 2011. \nHe has been working for the Institute of Solar and Terrestrial Physics and for Irkutsk State Transport University as a senior researcher and as a Professor. As an expert in his field, he is a member of the Radio-engineering Science Council of Siberian Federal University and a Head of State Examination Commission of Moscow State Aviation University.\nHis research interests are: ionosphere scintillation research, science education, navigation solutions for transport, and space weather impacts on GNSS.",institutionString:null,position:null,outsideEditionCount:null,totalCites:0,totalAuthoredChapters:"2",totalChapterViews:"0",totalEditedBooks:"1",institution:null}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:{id:"213157",title:"Dr.",name:"Jonathan",middleName:null,surname:"Becedas",slug:"jonathan-becedas",fullName:"Jonathan Becedas",profilePictureURL:"https://mts.intechopen.com/storage/users/213157/images/system/213157.jpeg",biography:"Dr. Jonathan Becedas is an Electrical Engineer and Industrial Engineer who graduated with honors. He holds a Master in Research and a PhD in Mechatronics from the University of Castilla-La Mancha (UCLM), Spain. He is the author of nearly 100 fully refereed scientific papers and has participated in over 20 competitive research projects, many of them for NASA, ESA, and the European Commission. He held a position of Researcher and Associate Professor at the University of Castilla-La Mancha (Spain) from 2002 until 2009 and was a Research Associate at the University of Leicester (United Kingdom) from 2009 until 2011. He was Head of the Robotics Department in Ixion Industry and Aerospace from 2011 until 2013. In that year he joined Elecnor Deimos Satellite Systems as Research Manager. He is currently R&D Manager and Head of the Projects Department in Elecnor Deimos Satellite Systems, where he coordinates R&D projects and satellite missions.",institutionString:"Elecnor Deimos Satellite Systems",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"4",totalChapterViews:"0",totalEditedBooks:"0",institution:null},coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"637",title:"Spatial Analysis",slug:"spatial-analysis"}],chapters:[{id:"70189",title:"GNSS High-Rate Data and the Efficiency of Ionospheric Scintillation Indices",doi:"10.5772/intechopen.90078",slug:"gnss-high-rate-data-and-the-efficiency-of-ionospheric-scintillation-indices",totalDownloads:736,totalCrossrefCites:3,totalDimensionsCites:4,hasAltmetrics:0,abstract:"The work discusses the efficiency of different ionospheric scintillation indices. The new index D2fi based on the GNSS carrier phase observable was introduced. We analyze the accuracy of the phase measurements, in particular its dependence on the GNSS equipment thermal noises, multipath and external noises, and presettings of Phase Lock Loop and Code Delay Discriminator. The performance of DROTI, S4, σφ, and D2fi was considered for the case of high-rate data. The “sensitivity” and reliability of each index differs significantly and depends on the time resolution of the carrier phase data. The new index D2fi advantages are that it is easily derived and has a clear dependence on GNSS hardware and software features. D2fi was proven to be a useful tool to detect the small-scale ionospheric disturbances based on high-rate GPS carrier phase measurements.",signatures:"Vladislav V. Demyanov, Maria A. Sergeeva and Anna S. Yasyukevich",downloadPdfUrl:"/chapter/pdf-download/70189",previewPdfUrl:"/chapter/pdf-preview/70189",authors:[{id:"154597",title:"Prof.",name:"Vladislav",surname:"Demyanov",slug:"vladislav-demyanov",fullName:"Vladislav Demyanov"},{id:"299487",title:"Dr.",name:"Maria",surname:"Sergeeva",slug:"maria-sergeeva",fullName:"Maria Sergeeva"},{id:"307343",title:"Dr.",name:"Anna",surname:"Yasyukevich",slug:"anna-yasyukevich",fullName:"Anna Yasyukevich"}],corrections:null},{id:"68567",title:"The Influence of the Lower Ionospheric Disturbances on the Operating Conditions of Navigation Satellite Systems",doi:"10.5772/intechopen.88552",slug:"the-influence-of-the-lower-ionospheric-disturbances-on-the-operating-conditions-of-navigation-satell",totalDownloads:735,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"The study of the impact of ionospheric disturbances on the conditions of functioning of satellite communication and navigation systems and the development of methods to reduce this effect requires the development of methods for evaluating the parameters of ionospheric disturbances and their spatial and temporal distribution. Studies show that electron concentration disturbances, which can have a significant impact on the functioning of transionospheric radio channels, can occur both in the upper and lower ionosphere. At the same time, the methods of studying the dynamics of ionospheric disturbances in the lower ionosphere are not enough developed, and the interrelation of the lower and upper perturbations of the ionosphere is insufficiently studied. The aim of the work is an experimental study of disturbances of the upper and lower ionosphere in order to clarify the mechanisms of their relationship and study the spatiotemporal distribution of mid-latitude disturbances. The results obtained show that the contribution of the electron density disturbances in the D region to the total electron content of the ionosphere can be significant and considerably depends on the type of heliogeophysical processes.",signatures:"Boris Gavrilov, Yuriy Poklad and Iliya Ryakhovskiy",downloadPdfUrl:"/chapter/pdf-download/68567",previewPdfUrl:"/chapter/pdf-preview/68567",authors:[{id:"300632",title:"Prof.",name:"Boris",surname:"Gavrilov",slug:"boris-gavrilov",fullName:"Boris Gavrilov"},{id:"301271",title:"Dr.",name:"Yuriy",surname:"Poklad",slug:"yuriy-poklad",fullName:"Yuriy Poklad"},{id:"301272",title:"Dr.",name:"Ilya",surname:"Ryakhovskiy",slug:"ilya-ryakhovskiy",fullName:"Ilya Ryakhovskiy"}],corrections:null},{id:"70213",title:"Real-Time Monitoring of Ionospheric Irregularities and TEC Perturbations",doi:"10.5772/intechopen.90036",slug:"real-time-monitoring-of-ionospheric-irregularities-and-tec-perturbations",totalDownloads:854,totalCrossrefCites:2,totalDimensionsCites:3,hasAltmetrics:1,abstract:"The ionosphere is a part of the upper atmosphere that is a threat to GNSS and satellite telecommunication systems. In this chapter, we will dive into the GNSS real-time monitoring of ionospheric irregularities and TEC perturbations, with a focus on the detection of small- and medium-scale traveling ionospheric disturbances (TIDs) for natural hazard applications. We will describe the Variometric Approach for Real-Time Ionosphere Observation (VARION) algorithm, which is capable of estimating TEC variations in real time, and it was used to detect tsunami-induced TIDs. In particular, the analytical and physical implications of applying the VARION algorithm both to GNSS dual-frequency MEO (medium Earth orbit) and GEO (geostationary orbit) satellites will be provided, thus highlighting its relevance for natural hazard early warning systems and real-time monitoring of ionospheric irregularities.",signatures:"Giorgio Savastano and Michela Ravanelli",downloadPdfUrl:"/chapter/pdf-download/70213",previewPdfUrl:"/chapter/pdf-preview/70213",authors:[{id:"303941",title:"Dr.",name:"Giorgio",surname:"Savastano",slug:"giorgio-savastano",fullName:"Giorgio Savastano"},{id:"303943",title:"M.Sc.",name:"Michela",surname:"Ravanelli",slug:"michela-ravanelli",fullName:"Michela Ravanelli"}],corrections:null},{id:"72133",title:"GPS Signal Multipath Error Mitigation Technique",doi:"10.5772/intechopen.92295",slug:"gps-signal-multipath-error-mitigation-technique",totalDownloads:619,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"The performance of GPS receiver depends on the accuracy of the range measurements. The predominant errors in range measurements are due to propagation path delays, making the measured range longer than it would be, if the signal has not reflected or refracted while propagating. In this chapter, an algorithm is proposed to mitigate the multipath error on the pseudorange measured from L1 carrier frequency. The error is estimated considering the linear combination of the GPS measurements and carrier frequencies of L band, viz. L1 and L2. This algorithm exploits the random nature of the multipath error and it avoids complex calculations involving sensitive parameter like reflection coefficient of the nearby reflectors. The multipath error is mitigated for standalone GPS receiver located in Indian subcontinent. Implementation of the algorithm shows pseudorange error due to multipath varied from 7 to 52 m, where the signals of low elevation satellites are most affected. GPS receiver position is calculated by considering multipath error corrected pseudoranges of all the visible satellites. This resulted in maximum error reduction of 30 m in receiver position estimates. This mitigation technique will be useful in selecting the site for GPS receiving antenna, where reflection coefficients are difficult to measure.",signatures:"Bharati Bidikar, Babji Prasad Chapa, Mogadala Vinod Kumar and Gottapu Sasibhushana Rao",downloadPdfUrl:"/chapter/pdf-download/72133",previewPdfUrl:"/chapter/pdf-preview/72133",authors:[{id:"227785",title:"Dr.",name:"Bharati",surname:"Bidikar",slug:"bharati-bidikar",fullName:"Bharati Bidikar"},{id:"227794",title:"Prof.",name:"Sashibhushana Rao",surname:"Gottapu",slug:"sashibhushana-rao-gottapu",fullName:"Sashibhushana Rao Gottapu"},{id:"312020",title:"Mr.",name:"Babji Prasad",surname:"Chapa",slug:"babji-prasad-chapa",fullName:"Babji Prasad Chapa"},{id:"320171",title:"Dr.",name:"Mogadala Vinod",surname:"Kumar",slug:"mogadala-vinod-kumar",fullName:"Mogadala Vinod Kumar"}],corrections:null},{id:"70180",title:"The Impact of Space Radiation Environment on Satellites Operation in Near-Earth Space",doi:"10.5772/intechopen.90115",slug:"the-impact-of-space-radiation-environment-on-satellites-operation-in-near-earth-space",totalDownloads:1238,totalCrossrefCites:6,totalDimensionsCites:10,hasAltmetrics:0,abstract:"Energetic particles and electromagnetic radiation (EM) from solar events and galactic cosmic rays can bombard and interact with satellites’ exposed surfaces, and sometimes possess enough energy to penetrate their surface. Among other known effects, the scenario can cause accelerated orbit decay due to atmospheric drag, sporadic and unexplainable errors in functions of sensitive parts, degradation of critical properties of structural materials, jeopardy of flight worthiness, transient and terminal health hazard to both onboard passengers and astronauts, and sometimes a catastrophic failure that can abruptly end satellite mission. The understanding of the dynamics of the space radiation environment and associated effects is critically important for satellites design and operation in ionospheric plasma environment, in which satellites are designed to function. In this chapter we review some satellite anomalies associated with the space radiation environment and conclude with mitigation effort that can reduce such impact.",signatures:"Victor U. J. Nwankwo, Nnamdi N. Jibiri and Michael T. Kio",downloadPdfUrl:"/chapter/pdf-download/70180",previewPdfUrl:"/chapter/pdf-preview/70180",authors:[{id:"94563",title:"Dr.",name:"Nnamdi",surname:"Jibiri",slug:"nnamdi-jibiri",fullName:"Nnamdi Jibiri"},{id:"300878",title:"Dr.",name:"Victor",surname:"Nwankwo",slug:"victor-nwankwo",fullName:"Victor Nwankwo"},{id:"310318",title:"Dr.",name:"Michael",surname:"Kio",slug:"michael-kio",fullName:"Michael Kio"}],corrections:null},{id:"69333",title:"Ionospheric Scintillation Modeling Needs and Tricks",doi:"10.5772/intechopen.88313",slug:"ionospheric-scintillation-modeling-needs-and-tricks",totalDownloads:463,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"The wavelength of the radio-wave satellite signal is of the order of the minimal small-scale ionospheric irregularities (i.e., a few centimeters). As the satellite signal passes through the ionosphere, its interaction with the ionospheric irregularity structures causes refraction, reflection, and polarization in the satellite signal. Ionospheric irregularities degrade the trans-ionospheric radio-wave signal quality, between the satellite and the receivers, due to scintillation. The physics-based model often fails to produce global morphology during the extreme solar events, whereas empirical models based on the ionospheric scintillation data demonstrate better quality to forecast the scintillation effects during extreme solar event. It is really tricky to make a scintillation model that is sensitive to low and high solar activities as well as extreme solar events simultaneously. In the presented book chapter, we will discuss/review the needs and tricks of modeling ionospheric scintillation during extreme solar events as well as all weather and latitudinal cases. There are several aspects that influence the scintillation occurrence, its strength, and global distribution. The latitudinal dependence, local weather, solar/geomagnetic activity conditions, and local times are the widely accepted factors that control and influence ionospheric scintillation most. This book chapter discusses all these aspects and also suggests the ways to cast aside those factors that led to the wrong measure of scintillation indices.",signatures:"Shishir Priyadarshi",downloadPdfUrl:"/chapter/pdf-download/69333",previewPdfUrl:"/chapter/pdf-preview/69333",authors:[{id:"301174",title:"Dr.",name:"Shishir",surname:"Priyadarshi",slug:"shishir-priyadarshi",fullName:"Shishir Priyadarshi"}],corrections:null},{id:"70862",title:"Earth Observation Technologies: Low-End-Market Disruptive Innovation",doi:"10.5772/intechopen.90923",slug:"earth-observation-technologies-low-end-market-disruptive-innovation",totalDownloads:817,totalCrossrefCites:3,totalDimensionsCites:3,hasAltmetrics:1,abstract:"After decades of traditional space businesses, the space paradigm is changing. New approaches to more efficient missions in terms of costs, design, and manufacturing processes are fostered. For instance, placing big constellations of micro- and nano-satellites in Low Earth Orbit and Very Low Earth Orbit (LEO and VLEO) enables the space community to obtain a huge amount of data in near real-time with an unprecedented temporal resolution. Beyond technology innovations, other drivers promote innovation in the space sector like the increasing demand for Earth Observation (EO) data by the commercial sector. Perez et al. stated that the EO industry is the second market in terms of operative satellites (661 units), micro- and nano-satellites being the higher share of them (61%). Technological and market drivers encourage the emergence of new start-ups in the space environment like Skybox, OneWeb, Telesat, Planet, and OpenCosmos, among others, with novel business models that change the accessibility, affordability, ownership, and commercialization of space products and services. This chapter shows some results of the H2020 DISCOVERER (DISruptive teChnOlogies for VERy low Earth oRbit platforms) Project and focuses on understanding how micro- and nano-satellites have been disrupting the EO market in front of traditional platforms.",signatures:"Silvia Rodriguez-Donaire, Miquel Sureda, Daniel Garcia-Almiñana, Eloi Sierra, Jose S. Perez, Peter C.E. Roberts, Jonathan Becedas, Georg H. Herdrich, Dhiren Kataria, Ronald Outlaw, Leonardo Ghizoni, Rachel Villain, Alexis Conte, Badia Belkouchi, Kate Smith, Steve Edmondson, Sarah Haigh, Nicholas H. Crisp, Vitor T.A. Oiko, Rachel E. Lyons, Stephen D. Worral, Sabrina Livadiotti, Claire Huyton, Luciana A. Sinpetru, Rosa M. Domínguez, David González, Francesco Romano, Yung-An Chan, Adam Boxberger, Stefanos Fasoulas, Constantin Traub, Victor Jungnell, Kristian Bay, Jonas Morsbøl, Ameli Schwalber and Barbara Heißerer",downloadPdfUrl:"/chapter/pdf-download/70862",previewPdfUrl:"/chapter/pdf-preview/70862",authors:[{id:"213157",title:"Dr.",name:"Jonathan",surname:"Becedas",slug:"jonathan-becedas",fullName:"Jonathan Becedas"},{id:"29453",title:"Dr.",name:"Silvia",surname:"Rodriguez-Donaire",slug:"silvia-rodriguez-donaire",fullName:"Silvia Rodriguez-Donaire"},{id:"43527",title:"Dr.",name:"Daniel",surname:"Garcia-Almiñana",slug:"daniel-garcia-alminana",fullName:"Daniel Garcia-Almiñana"},{id:"213159",title:"MSc.",name:"David",surname:"González",slug:"david-gonzalez",fullName:"David González"},{id:"300754",title:"Dr.",name:"Miquel",surname:"Sureda",slug:"miquel-sureda",fullName:"Miquel Sureda"},{id:"300755",title:"Mr.",name:"Santiago",surname:"Perez",slug:"santiago-perez",fullName:"Santiago Perez"},{id:"301368",title:"M.Sc.",name:"Eloi",surname:"Sierra Salvadó",slug:"eloi-sierra-salvado",fullName:"Eloi Sierra Salvadó"},{id:"307268",title:"Dr.",name:"Peter",surname:"Roberts",slug:"peter-roberts",fullName:"Peter Roberts"},{id:"307269",title:"Dr.",name:"Georg",surname:"Herdrich",slug:"georg-herdrich",fullName:"Georg Herdrich"},{id:"307270",title:"Dr.",name:"Dhiren",surname:"Kataria",slug:"dhiren-kataria",fullName:"Dhiren Kataria"},{id:"307271",title:"Mr.",name:"Leonardo",surname:"Ghizoni",slug:"leonardo-ghizoni",fullName:"Leonardo Ghizoni"},{id:"307272",title:"Mr.",name:"Rachel",surname:"Villain",slug:"rachel-villain",fullName:"Rachel Villain"},{id:"307273",title:"Ms.",name:"Barbara",surname:"Heißerer",slug:"barbara-heisserer",fullName:"Barbara Heißerer"},{id:"307274",title:"Ms.",name:"Ameli",surname:"Schwalber",slug:"ameli-schwalber",fullName:"Ameli Schwalber"},{id:"307275",title:"Mr.",name:"Jonas",surname:"Morsbøl",slug:"jonas-morsbol",fullName:"Jonas Morsbøl"},{id:"307276",title:"Mr.",name:"Kristian",surname:"Bay",slug:"kristian-bay",fullName:"Kristian Bay"},{id:"307277",title:"Mr.",name:"Victor",surname:"Jungnell",slug:"victor-jungnell",fullName:"Victor Jungnell"},{id:"307278",title:"Dr.",name:"Constantin",surname:"Traub",slug:"constantin-traub",fullName:"Constantin Traub"},{id:"307279",title:"Dr.",name:"Stefanos",surname:"Fasoulas",slug:"stefanos-fasoulas",fullName:"Stefanos Fasoulas"},{id:"307281",title:"Dr.",name:"Adam",surname:"Boxberger",slug:"adam-boxberger",fullName:"Adam Boxberger"},{id:"307283",title:"Dr.",name:"Francesco",surname:"Romano",slug:"francesco-romano",fullName:"Francesco Romano"},{id:"307285",title:"Dr.",name:"Nicholas",surname:"Crisp",slug:"nicholas-crisp",fullName:"Nicholas Crisp"},{id:"307286",title:"Dr.",name:"Vitor",surname:"Oiko",slug:"vitor-oiko",fullName:"Vitor Oiko"},{id:"307415",title:"Mr.",name:"Alexis",surname:"Conte",slug:"alexis-conte",fullName:"Alexis Conte"},{id:"307417",title:"Ms.",name:"Badia",surname:"Belkouchi",slug:"badia-belkouchi",fullName:"Badia Belkouchi"},{id:"307419",title:"Dr.",name:"Steve",surname:"Edmondson",slug:"steve-edmondson",fullName:"Steve Edmondson"},{id:"307420",title:"Dr.",name:"Sarah",surname:"Haigh",slug:"sarah-haigh",fullName:"Sarah Haigh"},{id:"307421",title:"Ms.",name:"Kate",surname:"Smith",slug:"kate-smith",fullName:"Kate Smith"},{id:"307422",title:"Ms.",name:"Rachel",surname:"Lyons",slug:"rachel-lyons",fullName:"Rachel Lyons"},{id:"307423",title:"Dr.",name:"Stephen",surname:"Worrall",slug:"stephen-worrall",fullName:"Stephen Worrall"},{id:"307424",title:"Ms.",name:"Sabrina",surname:"Livadiotti",slug:"sabrina-livadiotti",fullName:"Sabrina Livadiotti"},{id:"307425",title:"Ms.",name:"Claire",surname:"Huyton",slug:"claire-huyton",fullName:"Claire Huyton"},{id:"307426",title:"Ms.",name:"Luciana",surname:"Sinpetru",slug:"luciana-sinpetru",fullName:"Luciana Sinpetru"},{id:"307428",title:"Ms.",name:"Rosa María",surname:"Domínguez",slug:"rosa-maria-dominguez",fullName:"Rosa María Domínguez"},{id:"307430",title:"Dr.",name:"Yung-An",surname:"Chan",slug:"yung-an-chan",fullName:"Yung-An Chan"},{id:"307431",title:"Mr.",name:"Ron",surname:"Outlaw",slug:"ron-outlaw",fullName:"Ron Outlaw"}],corrections:null},{id:"72354",title:"A Survey on Small Satellite Technologies and Space Missions for Geodetic Applications",doi:"10.5772/intechopen.92625",slug:"a-survey-on-small-satellite-technologies-and-space-missions-for-geodetic-applications",totalDownloads:906,totalCrossrefCites:3,totalDimensionsCites:6,hasAltmetrics:0,abstract:"Advances in microelectronics, materials, combined with affordable and frequent launch opportunities has led to a revolution which consists of small satellite missions used for technology validation, Earth observation, space exploration. Small satellites are now being developed in large volumes for mega-constellations for Earth observation, Internet of Things (IoT) and low latency communications (internet) thus democratizing space and making new space applications a reality. Advances in small satellite platforms, miniaturization of instruments and the availability of low-cost launches for small satellites, can enable new, geodetic missions which can benefit from the use of constellations of small satellites. 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\r\n\tCytomegalovirus (CMV) is a serious infection virus that is related to the herpes viruses and causes chickenpox and mononucleosis. CMV can develop in people who are immunocompromised and immunodeficient, called opportunistic infections. Opportunistic infections only occur if your immune system is quite weakened. Most adults carry CMV but are unaware of it because the virus cannot produce disease. In people with severely weakened immune systems, CMV can make a person feel as though they have mono. CMV can also cause serious diseases in different parts of the body. CMV spreads from person to person through body fluids, such as blood, saliva, urine, semen, and breast milk. Women who develop an active CMV infection during pregnancy can pass the virus to their neonates, who might then experience symptoms. Human cytomegalovirus (HCMV) infection induces both innate immune responses including Natural Killer cells as well as adaptive humoral and cell-mediated (CD4+ helper, CD8+ cytotoxic and γδ T cell) responses which lead to the resolution of acute primary infection. Therefore, recognition of immunopathology, pathogenesis and immune response against CMV are necessary.
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However, this comes at an environmental cost, for example, over 600 kt of CO2 was emitted by London’s bus fleet in 2015 [1]. It is these carbon emissions and their link to climate change that have provided one of the major drivers in recent years to develop and deploy alternative technologies for bus propulsion [2]. Other emissions associated with diesel vehicles such as NO
Comparison of various technologies for the power and energy densities (based on Ref. [
In order to address the environmental concerns posed by diesel buses, a number of technologies are being investigated and implemented. The most widespread of these are diesel-hybrid buses, which make use of an on-board energy storage system to effectively recycle captured kinetic energy obtained through regenerative braking. Although hybrid buses are capable of significantly reducing fuel consumption, they are still reliant on diesel as the primary fuel source and hence do not address the fundamental problems associated with emission that come from using diesel as a fuel. As such, there has in recent years been an increased focus on the development of zero emissions buses, with two main competing technologies. These are battery electric buses and hydrogen fuel cell (FC), both of which exhibit zero operating emissions, hence eliminates the environmental and health issues associated with diesel buses [11]. Such technology solutions are less mature and result in significant changes to the propulsion system. Although these technologies have been deployed in operational bus fleets, there remain a number of barriers to widespread deployment.
\nLondon has one of the most comprehensive and busiest public transport networks in the world, operated by Transport for London (TfL). There are over 9000 buses in operation [12], which are estimated to account for 21% of the CO2 emissions in London [7], 63% of NO
Timeline of the milestones for the London low emission bus deployment.
Within this chapter, the development of low emission bus propulsion technologies will be discussed, through the evolution of diesel to diesel hybrid buses and onto the development and deployment of battery electric and FC buses. The aim is to outline the benefits of such technologies and the barriers that exist to their widespread implementation from both a technical and economic perspective. Part 2 discusses the implementation of diesel electric hybrid buses and their evolution from diesel buses. Parts 3 and 4 consider battery electric buses and fuel cell buses, respectively, whilst part 5 provides a comparison of these emerging technologies.
\nThe principle difference between diesel hybrid buses and diesel buses is the inclusion of an electrical energy storage system in conjunction with an electrical motor/generator. The primary source of energy is still the diesel engine; however, the inclusion of the electrical system provides a number of advantages such as facilitating regenerative braking and allowing reduced idling time [17]. The utilisation of a hybrid system results in improvements fuel efficiency and emissions, although these come at the price of additional cost and complexity [17].
\nThe integration of the electrical energy system can be utilised through a number of configurations, with the common options being the series, parallel and series-parallel hybrid configurations, as shown in Figure 3. In a series hybrid drivetrain, the mechanical output from the diesel engine is converted into electrical power via a generator when operating at its most efficient loading. This is supplemented with a battery to provide for the electric drive motor requirements. Since the propulsion needs are met by an electric motor, this results in the complete decoupling between the diesel engine and the wheels, meaning that engine control is not dependent on vehicle speed so offering additional flexibility [18]. This is a major advantage of series hybrid drivetrains, where the engine can operate at any point on its speed-torque map, which is impossible for conventional vehicles. Therefore, the engine is capable of constantly operating at near optimum load, which minimises fuel consumption and emission [19].
\nSchematic of the three available layouts for the propulsion system of a diesel/electric hybrid drive train.
The parallel hybrid configuration maintains the direct mechanical link between the diesel engine and the wheels, using the battery for regenerative braking and supplementing the peak power demands. The main advantages over the series hybrid are that the additional generator is no longer needed so has higher efficiency as well as reducing the size of the required drive motor. The parallel configuration, however, does not decouple the diesel engine from the wheels and hence operation is directly linked to the vehicle speed hence for low speed city operation the ICE will often operate at a low efficiency [20]. As a result, the parallel configuration is more appropriate for longer distance and higher speed routes. The series-parallel hybrid can operate in either the series or parallel configurations and so can utilise the advantages of both systems; however, the additional complexity and capital cost of the system mean that they are currently not a viable option for transportation applications [19]. The most popular option for city buses is the series configuration due to the simplicity of a single drive system as well as higher efficiency during city driving where buses have a start-stop traffic pattern with generally low speed operation [19].
\nThe benefits offered by the hybridisation of the drive system relate to the increase in fuel economy and reduction in emissions compared to a diesel bus and can be attributed to the following points.
\nOn average buses idles for around 30–44% of urban driving time [21]. By using a hybrid system, the vehicle can turn off the engine to prevent idling and low loads because it can use the electrical energy storage and motor for initial acceleration. This can save 5–8% of fuel consumption [17].
A significant amount of energy is lost and dissipated by heat due to friction during conventional braking. When a hybrid vehicle is braking, the drive motor can work as generator to charge the electrical energy storage system and thus recycle some of the energy used to propel the bus. Typically, 10–20% of the kinetic energy is recovered.
In a conventional bus, the diesel engine needs to be large enough to provide for all of the peak transient power demands. A hybrid vehicle is able to use the electrical system to provide for a portion of these peak demands, and therefore, the engine can be downsized [17, 19].
A diesel engine operates at its lowest efficiency during low load and low speed operation. The electrical system can drive the electric motor to power the bus during low load and start-up to avoid this. It is expected that diesel hybrid technology can achieve reductions of between 24 and 37% CO2 emission [22], 21% to NO
In contrast to these benefits, the hybridisation of the drive system has a number of drawbacks. These predominately amount to the additional capital cost, where a diesel hybrid typically costs £300,000, this is £110,000 more than a conventional diesel bus and constitutes an increase of about 50% [23]. The additional complexity of both the drive system and its control results in additional maintenance time and cost, where a diesel hybrid typically requires 50% more maintenance time than a conventional diesel bus [22].
\nInitially a trial consisting of eight diesel hybrid buses was carried out in 2007 and was found to have very high (96%) customer support [24]. After analysing the trial, the official deployment of diesel hybrid buses began in central London. The number of diesel hybrid buses has steadily increased, where in 2015, more than 1200 diesel hybrid buses were in operation in London, as can be seen in Figure 4, and exceed the target of 1700 in 2016 [12]. This consists of old buses redesigned for hybrid operation and new designs such as the new Routemaster.
\nTotal number and percentage of the TfL bus fleet of diesel-hybrid buses in operation. Data from Ref. [
The impact of the deployment of the low emission bus fleets has already begun to have an impact on emissions in London, as shown in Figure 5. In the last few years, emissions of NO
Expected reduction in CO2 and NO
The performance of the diesel hybrid bus fleet in London is very variable, as might be expected due to differing models and routes. It was claimed that the average Euro V bus achieved a fuel economy of 32.9 l/100 km in London [9]. The reported fuel economy of diesel hybrid buses operating in London is presented in Table 1. As may be expected, the type of bus and bus route significantly affects the fuel economy, where a single decker bus generally exhibits a higher fuel economy than a double-decker bus. It was found that the introduction of diesel hybrid technology improved the fuel economy on nearly all routes; however, there were a couple of discrepancies to this, such as on the E8 bus route where the fuel economy actually decreased. The introduction of the new Routemaster bus appears to provide a slight improvement over previous diesel hybrid buses; however, there appears to be significant discrepancies between the recorded and expected performance. Results released by TfL in 2014 suggest a fuel economy in the range of 38.2–45.6 l/100 km, whereas it is claimed by the manufacturer that a fuel economy of 24.4 l/100 km was recorded on the 159 bus route. Unfortunately, the details for these results are not available and so it is difficult to determine the validity of the results. This discrepancy could be the result of a number of factors such as the route topology, traffic conditions, driving style and passenger conditions.
\nBus type | \nRoute | \nDiesel | \nDiesel hybrid | \nYear | \nReferences |
---|---|---|---|---|---|
Fuel economy (l/100 km) | \nFuel economy (l/100 km) | ||||
Single decker (Euro V) | \n276 | \n44.8 | \n43.5 | \n2010 | \n[26] |
360 | \n36.7 | \n34.9 | |||
371 | \n34.1 | \n26.7 | |||
E8 | \n35.3 | \n42.2 | |||
129 | \n47.1 | \n33.6 | |||
Double decker (Euro V) | \n141 | \n60.1 | \n50.4 | \n2010 | \n[26] |
328 | \n65.7 | \n54.3 | |||
24 | \n49.6 | \n42.2 | |||
482 | \n50.4 | \n34.9 | |||
16 | \n50.4 | \n39.2 | |||
New routemaster (Euro V) | \n11 | \n60.1 | \n38.2 | \n2014 | \n[27] |
24/390 | \n52.3 | \n38.2 | |||
9 | \n72.4 | \n45.6 | |||
148 | \n56.5 | \n40.9 | |||
10 | \n64.2 | \n43.5 | |||
159 | \nNot available | \n24.4 | \n2013 | \n[28] |
Available data for diesel hybrid bus fuel economy in London. The values for l/100 km have been converted from miles per gallon using Litres100 km = (100*4.54609)/(1.609344*mpguk).
In summary, TfL has successfully introduced a large number of diesel hybrid buses into their bus fleet. This has resulted in a decrease in the emissions associated with the bus fleet, with considerable further reductions expected. It provides an example of the successful deployment of diesel hybrid buses into a large operational bus fleet to achieve reductions in emissions and fuel consumption. However, the increased cost and system complexity remain problematic.
\nThe battery electric bus, often described as a pure electric bus, uses an electric motor for propulsion and a battery for energy storage [29]. In most cases the battery is the primary energy source, although for trolley buses power is delivered from overhead cables during operation.
\nThe configuration for electric buses is typically fairly straightforward since it is basically a battery driving an electric motor to propel the vehicle [30], as shown in Figure 6. During braking it is also possible to make use of regenerative braking to recharge the battery during braking. The main battery technologies that have been used in transportation are Ni-MH, Zebra (Na-NiCL2) and lithium batteries [31]. The most promising of these are the lithium batteries, where three main categories exist, these being Li-ion, lithium polymer (LiPo) and Lithium-iron-phosphate (LiFePO4) batteries [32]. Most current buses use lithium-based batteries [33] due to their high power and energy densities and fast charging capabilities, although their high cost is still problematic [32]. A problem faced by all battery technologies is their cycle life; typically, these are short and hence require relatively regular replacement [34]. In addition to a battery pack, some buses utilise supercapacitors in conjunction with a battery as supercapacitors are much more effective in shielding batteries from high current load and thus increase battery life [35]; however, their low energy density means they are unsuitable to be used as the primary energy source, as shown in Figure 1. They do, however, have several key advantages over existing battery technologies, such as very high power densities and discharge rates as well as very long cycle life [34]. There is no simple answer to which battery technology is best, as it will depend on the application. Mahmoud et al. [36] carried out a detailed comparison study of different electric powertrains and concluded that a single technological choice would not satisfy the varied operational demands of transit services because electric buses are highly sensitive to the energy profile and operational demands. Electric buses are zero emission at the point of use and therefore offer great emission savings particularly in terms of local air pollution when compared to ICE or hybrid buses, as well as very high efficiency. However, there are a number of barriers to widespread deployment, the main ones are recharging time, vehicle range, infrastructure and cost [34].
\nBattery electric drive bus basic configuration.
Battery electric buses normally operate in one of two different forms: opportunity and overnight [32]. Opportunity e-buses have a smaller energy storage capacity that offers limited range but can be charged much quicker (5–10 minutes); while overnight e-buses have a much larger energy storage but at the cost of longer charging time (2–4 hour) [36]. These represent two different approaches for electric buses in the urban environment. The opportunity approach aims to minimise the weight of the battery pack by utilising frequent and fast recharging at points along the bus route, such as bus stops or the end of route [32]. This holds the promise of high efficiency and lower projected bus costs but requires a comprehensive recharging network [37]. Route flexibility of the bus is, however, limited, as it is required to follow the assigned bus route to recharge the battery. The overnight method utilises a large energy storage system to extend the range so that the bus can drive the entire route/day without recharging [37]. This holds the promise of greater route flexibility and convenience as well as utilising a centralised recharging infrastructure, but suffers from passenger loss due to increased battery weight as well as battery lifetime issues [38] and battery cost [34]. An alternative approach is offered by the Trolleybus, which has a small battery but receives power from overhead cables along the assigned route. This overcomes problems associated with range and recharging times but is very limited in terms of route flexibility.
\nThe process of recharging a battery electric bus can be completed through plug-in (conductive), wireless (inductive) or catenary (overhead power lines) charging. Plug-in charging requires a direct connection through a power cord [39] and is well-suited to overnight bus charging, but can be used in some instances for opportunity charging. This is popular due to its simplicity and high efficiency [39]. Wireless charging relies on induction between two coils, this is better suited to opportunity buses where recharging can take place along the route without the need for a physical connection [39], such as the PRIMOVE bus where charging is carried out at each end of the route and at five intermediate stops [40]. This form of charging, however, suffers from increased charging times and relatively low efficiency [39]. The trolleybus uses overhead catenary to provide power to the bus [41]. This type of charging exhibits high efficiency but requires an extensive network of overhead cables.
\nTable 2 shows a selection of operating pure electric buses in different locations and utilise a number of battery technologies and operating approaches. In 2015, there were an estimated 150,000 battery electric buses, mostly located in China, with a sixfold increase between 2014 and 2015 [42]. The electric bus market is growing quickly where it had a 6% share of global bus purchases in 2012 but is forecasted to grow to 15% by 2020 [43]. Battery electric bus development has been carried out all over the world with the largest shares in China, Europe and North America [44]. It is clear that some of the buses listed in Table 2 utilise more than one mode of operation to provide for the operational power requirements, such as the complete coach works bus, which uses both overnight and opportunity charging. The differences in operating regimes are reflected in the sizing of the batteries and as a result the range of the buses, where they vary from 5.9 kWh for the trolleybus design to >300 kWh for overnight charging. This will have a significant impact in terms of the bus’s battery costs; however, the charging infrastructure for overnight charging does not need to be as comprehensive as for the alternative methods.
\nManufacturer | \nLength | \nCapacity | \nBattery type | \nBattery capacity | \nType, range | \nDeployment location |
---|---|---|---|---|---|---|
ABB TOSA | \n18 m | \n135 | \nLithium titanate oxide | \n38 kWh | \nTrolley, on-route | \nSwitzerland |
BYD | \n12 m | \n40 | \nBYD Iron Phosphate | \n324 kWh | \nOvernight, 250 km | \nWorldwide |
Complete Coach Works | \n12 m | \n37 | \nLithium-iron Phosphate | \n213 kWh | \nOvernight/opportunity, 145 km | \nUS |
EBusco | \n12 m | \n76 | \nLithium-iron Phosphate | \n242 kWh | \nOvernight, 250 km | \nChina, Finland |
Hengtong EBus | \n12 m | \n70 | \nLithium Titanate | \n60.9 kWh | \nOpportunity, 39 km | \nChina |
New Flyer | \n12 m | \n40 | \nLithium-Ion | \n120 kWh | \nOpportunity, 72 km | \nUS, Canada |
Primove | \n12 m | \n44 | \nLithium-Ion | \n60 kWh | \nWireless, on-route | \nGermany |
Proterra | \n10 m | \n35 | \nLithium Titanate | \n74 kWh | \nOpportunity, 42 km | \nUS |
Siemens | \n8 m | \n40 | \nLithium-iron Phosphate | \n96 kWh | \nTrolley, on-route | \nAustria |
Sinautec | \n12 m | \n41 | \nUltra-Cap and Battery | \n5.9 kWh | \nTrolley, on-route | \nChina |
Selection of operating electric bus models worldwide [40].
London has been working on overnight e-bus demonstrations since 2012 and is also investigating the potential of opportunity e-bus technologies. From the overnight e-bus perspective, TfL has collaborated with BYD, which is one of the largest electric bus manufacturer in China, to test the potential of battery electric buses in London, starting from 2012 [45]. The first two battery electric buses were handed over to TfL in 2013 and then entered daily service on two central London routes, numbers 507 and 521, which were the first battery electric buses in London. These single-decker 12-metre BYD buses utilise Lithium-Iron-phosphate batteries and have demonstrated a range in excess of 250 km on a single charge in real world urban driving conditions [46]. The 507 and 521 bus routes are relatively short commuter service routes and were chosen so that the bus can start operating in the morning peak alongside the diesel bus fleet and return to the depot to recharge during the day before resuming service for the evening peak [34, 47]. The battery takes 4–5 hours to recharge when fully discharged and has been designed for a cycle life of more than 4000 cycles, meaning a 10-year battery lifetime under normal operating conditions [48]. The trail fleet was extended to six buses in the summer of 2014. The trail buses in London not only provide a zero emission environmental benefit but also have shown promising result in terms of both technical and economic performance, and hence TfL has taken further steps towards adopting this new clean technology in the capital. The development timeline and future plans for London electric buses are plotted in Figure 7.
\nNumber of electric buses in London.
The latest data in 2016 showed that there are currently 22 battery electric buses operating in London including 17 single-decker battery electric buses and five double-decker battery electric buses. This is a world first for double-decker battery electric buses, as shown in Figure 8, and entered service in May 2016. These are 10.2 m buses with a capacity of 81 passengers and a claimed range of 303 km. The battery is a Lithium-Iron-Phosphate battery with a capacity of 320 kWh [49]. They utilise a combination of both overnight and opportunity e-bus technology and will operate on route 69 in Central London. They will use a high powered wireless inductive charging system to top up their battery system at the beginning and end of this route to keep the bus operating throughout the entire day [50]. The recent double-decker electric buses have used wireless charging technology as part of innovative charging technology development. However, this is still far from a mature technology and requires a massive recharging infrastructure network [51]. The electric buses in London have shown promising performance on short commuter routes; however, pure e-buses are still best suited for shorter routes with operational flexibility and scope to recharge them in inter-peak periods due to the limit of present battery capacity and recharging technology [52].
\nThe first electric double-decker bus in the world (photo from Business Green, 2016).
In 2015, BYD and Alexander Dennis (ADL) announced a partnership to provide 51 further single-decker buses to route operator Go-Ahead with an expected delivery in late 2016 [53]. BYD will provide the batteries and electric chassis technology, and ADL will provide the bus body-building technology [54]. The cost of each bus is expected to be £350,000 [55].
\nIn summary, the recent development and deployment of battery electric buses in London have shown that electric buses are technically feasible. It can be seen that electric buses will also have an important role to play in the coming ULEZ implementation in 2020. However, more time is needed to evaluate the actual performance and address the key challenges facing electric buses such as limitations of battery technology that restricts range.
\nHydrogen fuel cells (FCs) are considered a clean energy source with the main benefits over ICEs of zero harmful emissions during operation and high efficiency [56]. Although many types of FCs exist, this paper will only consider the application of FCs in transportation, considering the operating temperature, start-up time and technology maturity, Proton Exchange Membrane Fuel Cell (PEMFC) offer most promising solution [57]. Significant research into solid oxide fuel cells (SOFCs) in transportation has been carried out [58–60], although these have yet to been applied in real world bus applications. A PEM FC uses hydrogen as the fuel, which, through an electrochemical reaction with oxygen (usually from air) generates electricity with water as the only by-product from the chemical process [61]. By replacing the internal combustion engine in conventional buses, FCs can be used as the primary energy source to power a bus with electrical energy, therefore, achieving zero operating emissions. An additional advantage over ICE’s comes from the higher efficiencies exhibited by FCs [62, 63]. However, there are a number of barriers that need to be overcome before widespread deployment can be achieved. These are primarily cost and infrastructure [64, 65]. FC powered buses cost approximately five times more than a conventional diesel bus with the similar power output [66], where they typically cost in excess of £1,000,000 [67], due primarily to the expensive FC stack and the small scale of production [68]. In addition, the widespread deployment of FC buses would require a significant investment in hydrogen refuelling infrastructure [64]. The implementation of FC buses has shown that the technology is a promising solution for zero emissions buses if these barriers can be overcome.
\nFigure 9 shows the configuration usually used in FC vehicles. The basic drive train utilises a FC to power the propulsion motor; however, FCs are not well suited to providing for the transient power demands associated with city driving buses [69–73]. As such, most FC buses utilise a form of energy storage in a series configuration to both address this and also to utilise regenerative braking [74]. An additional benefit of such an approach is that the size of the expensive fuel cell stack can be reduced [75]. The energy storage implemented is usually either electrochemical battery technology such as Li-ion or NiCd batteries or electrostatic supercapacitors (sometimes referred to as ultracapacitors). The choice between these depends on the particular design and requirements of the system, with batteries offering reasonable power and energy densities although they have a relatively short cycle life and supercapacitors offering poor energy densities but excellent power densities, as shown in Figure 1. Additionally, supercapacitors have very long lifetimes of up to 40 years [31].
\nSimplified architectures of FC drivetrain.
In a series configuration, there are three main modes of operation that can be utilised to provide for the buses power demands, as shown in Figure 10. Although these are the main modes of operation, the way these modes are utilised will depend on the control strategy implemented [76].
\nModes of operation for a series hybrid FC drive train [
Mode 1: The SC discharges to supplement the FC to provide for high transient power demands. This type of operation is expected to occur under heavy loads such as during acceleration or going uphill.
Mode 2: The FC will both power the load and use excess power to charge the SC. This is expected to occur under low loads, when the FC power output is higher than the required load.
Mode 3: The power from the FC and generated power from regenerative brake will both be used to charge the SC. This is only expected to occur when the drive motor is operating as a generator in the regenerative brake mode.
There have been a number of projects aimed at utilising FC technology for bus propulsion applications. Table 3 lists many of the projects currently in operation along with the FC size and energy storage used. The projects are split into two main categories depending on the relative size of the FC and energy storage systems. The majority of the current projects are FC dominant, whereby the FC is expected to provide for the majority of the propulsion needs. Alternatively there a few examples of battery dominant hybrids, where the battery is the main source of power with the FC used as a supplementary power source. It was announced in 2017 that the JIVE project is to implement 142 buses across nine European cities with 56 new FC buses in the UK, which will be the first large scale validation project of FC bus fleets [78].
\nProject | \nFleet | \nYear | \nLocation | \nLength (m) | \nFC size (kW) | \nBattery type | \nBattery size (kWh) | \nDrive type |
---|---|---|---|---|---|---|---|---|
JHFC | \n2 | \n2006 | \nTokoname, Japan | \n10.5 | \n180 | \nNickel Metal Hydride | \nNot available | \nFC dominant hybrid |
University of Delaware | \n2 | \n2007 | \nDewark, US | \n6.7 | \n40 | \nNiCad | \n60 | \nBattery dominant hybrid |
TriHyBu | \n1 | \n2009 | \nNeratovice, Czech Republic | \n12 | \n48 | \nLithium Ion | \n26 | \nBattery dominant hybrid |
BurbankBus | \n1 | \n2010 | \nBurbank, US | \n10.7 | \n32 | \nLithium Titanate | \n54 | \nBattery dominant hybrid |
HySUT | \n2 | \n2010 | \nTokyo, Japan | \n10.5 | \n180 | \nNickel Metal Hydride | \nNot available | \nFC dominant hybrid |
NFCBP | \n1 | \n2010 | \nSan Francisco, US | \n12.2 | \n32 | \nLithium Ion | \nNot available3 | \nFC APU Compound |
Toyota FCHV | \n1 | \n2010 | \nToyota City, Japan | \n10.5 | \n180 | \nNickel Metal Hydride | \nNot available | \nFC dominant hybrid |
NFCBP | \n4 | \n2010 | \nHartford, US | \n12.2 | \n120 | \nLithium Ion | \n17.43 | \nFC dominant hybrid |
CHIC | \n8 | \n2010 | \nLondon, UK | \n12 | \n75 | \nSupercapacitor | \n0.5 | \nFC dominant hybrid |
CHIC | \n3 | \n2011 | \nMilan, Italy | \n11.9 | \n120 | \nLithium Ion | \n26 | \nFC dominant hybrid |
SunLine1 | \n6 | \n2011 | \nThousand Palms, US | \n12.2 | \n150 | \nNanophosphate Li-ion | \n11 | \nFC dominant hybrid |
NFCBP | \n12 | \n2011 | \nMulti-city, US | \n12.2 | \n120 | \nLithium Ion | \n17.4 | \nFC dominant hybrid |
CHIC | \n4 | \n2011 | \nCologne, Germany | \n18.4 | \n150 | \nNiMeH and Supercapacitor | \n23 and 0.6 | \nFC dominant hybrid |
CHIC | \n5 | \n2011 | \nAargau, Switzerland | \n11.9 | \n120 | \nLithium Ion4 | \n26.94 | \nFC dominant hybrid |
CHIC | \n5 | \n2012 | \nOslo, Norway | \n13 | \n150 | \nLithium Ion | \n17.5 | \nFC dominant hybrid |
NIP, CHIC | \n6 | \n2012 | \nHamburg, Germany | \n12 | \n120 | \nLithium Ion | \n26 | \nFC dominant hybrid |
CHIC | \n5 | \n2013 | \nBolzano, Italy | \n11.9 | \n120 | \nLithium Ion | \n26 | \nFC dominant hybrid |
HyTransit, HighVLO City | \n14 | \n2014 | \nAberdeen, UK | \n12.2 | \n150 | \nNot available | \nNot available | \nFC dominant hybrid |
HighVLO City | \n5 | \n2014 | \nBrussels, Belgium | \n12.2 | \n150 | \nNot available | \nNot available | \nFC dominant hybrid |
NFCBP2 | \n1 | \n2014 | \nAustin, US | \n10.7 | \n30 | \nLithium Titanate | \n54 | \nBattery dominant hybrid |
NFCBP2 | \n1 | \n2014 | \nBirmingham, US | \n9.8 | \n75 | \nLithium Titanate | \n54 | \nBattery dominant hybrid |
London has been involved with the testing and deployment of FC buses, Figure 11 shows the evolution of FC bus implementation in London. Initially, this was through the EU funded Clean Urban Transport for Europe (CUTE) project, which aimed at introducing hydrogen FC buses into European cities, where a test run of three buses were operated on the RV1 bus route between 2004 and 2006, this was increased to five buses from 2007 to 2009 [83]. London is now part of Clean Hydrogen in European Cities (CHICs) project with the first deployment in full service of the next generation of FC bus in 2011 and is expected to continue until 2019. There are currently eight Hydrogen buses operating in Central London as part of the CHIC project, fully covering the RV1 bus route, which is 9.7 km in length [83]. It is expected that by 2017 a further two buses developed as part of the 3Emotion project will be deployed through Van Hool [84]. The buses operate for 16–18 hours/day, before returning to the depot for refuelling at the central depot, which takes <10 minutes [85]. The workshop, which is responsible for routine maintenances and hydrogen management, was specifically designed and built for hydrogen FC buses [86]. The hydrogen has been transported in liquid form to the depot and converted into gaseous form to refuel buses [83], it is then stored on site in gaseous form at 500 bar [86].
\nLondon FC hydrogen bus development timeline (bus photos from Citaro, TfL, Van Hool, 2016).
The buses themselves have developed throughout this project, where the first generation was powered only by a FC. These utilised a 250 kW fuel cell [82] and achieved a hydrogen economy of 18.4–29.1 kg H2/100 km [87]. The buses deployed as part of the CHIC project utilised a series hybrid configuration, with a 75 kW PEM FC from Ballard and a 0.5 kWh Bluways supercapacitor energy storage system [88]. This introduction of the hybrid system significantly reduced the hydrogen economy to <10 kg H2/100 km [87] and is one of the most significant results of the CHIC project in London. Figure 12 shows that the fuel economy of the buses operated as part of the CHIC project showed considerable improvements over those in the CUTE project. It can also be seen that the London buses performed better than the CHIC target, exceeding it by nearly 50%. For all of the London FC buses, the hydrogen is stored as a compressed gas at 350 bar, with the gas cylinders stored on the roof of the bus [82].
\nAverage fuel consumption of FC buses in CHIC project (figure from FCH JU, 2016) [
Between 2011 and 2016, the FC buses in operation in London have covered over 1.1 million kilometres [89], and a number of the FC buses have achieved the milestone of 20,000 hours of operation [90]. This reflects the improvement of availability seen over the course of the deployment of CHIC’s London fleet. Figure 13 shows the availability from January 2012 until May 2015. The monthly availability of London FC buses has also significantly increased after the availability upgrade program carried out in 2014. The availability is expected to improve to over 85% by the end of the CHIC project as operators gain more operational and problem-solving experience.
\nAvailability of London FC buses in CHIC project (figure from FCH JU, 2016) [
Apart from the technical and economic improvements, the London trail buses have also proven that the technology became more viable because of the full working schedule, direct diesel replacement, centralised infrastructure and high public acceptance [86]. The trial test of FC-powered buses projects has provided promising performance as a long-term solution to zero emission transportation.
\nThis part aims at to provide a comparison of the current state of low emission and zero emission bus systems. Diesel hybrid buses have been developed and deployed as a means of achieving emissions reductions, where a number of advantages in terms of efficiency, emissions and fuel consumption can be seen over diesel buses. There are, however, a number of problems associated with their widespread deployment. The first of these is the cost and is due to the additional components necessary for the electrical system. Second, the inclusion of the electrical system necessitates a significantly more complicated configuration [19]. Third, although diesel hybrid buses can offer significant improvements in terms of CO2 and NO
Zero emission option | \nOpportunity E-bus | \nOvernight E-bus | \nTrolley E-bus | \nFuel cell bus |
---|---|---|---|---|
Daily range | \n4 | \n3 | \n1 | \n2 |
Route flexibility | \n3 | \n1 | \n4 | \n1 |
Refuelling time | \n2 | \n3 | \nNot available | \n1 |
Infrastructure | \n3 | \n2 | \n4 | \n1 |
Fuel availability | \n1 | \n1 | \n1 | \n4 |
Clean source | \n1 | \n1 | \n1 | \n4 |
Cost | \n3 | \n1 | \n2 | \n4 |
High level comparison of operational performance of zero emission bus concepts.
Notes: 1, best; 4, worst.
Throughout this chapter, the main technologies being implemented to meet the low emissions requirements have been presented. The most promising for these in terms of zero emissions are electric and FC buses; however, it is clear that there are still significant barriers to their widespread implementation. Following on from the challenges identified in the comparison section a number of challenges for future developments have been identified.
\nFor electric buses, it is clear that further improvements to battery technology are required in terms of their energy densities and lifetime as well as the development of an effective charging infrastructure. The challenges are somewhat dependant on whether the bus is intended to use the overnight or opportunity charging schemes. For overnight charging, the charging infrastructure can be centralised; however, this necessitates very large power requirements for the charging infrastructure, additionally the range of the buses needs to be addressed through battery developments. The opportunity charging schemes a comprehensive and distributed charging network. In most cases, this requires the development of high efficiency and power wireless charging technologies.
\nThe future development of FC buses requires development in a broader range of areas. This includes further work on individual components such as the FC stack and hydrogen storage. The FC stack is still the most expensive component of the FC bus. The further development of the control strategies for hybridised buses held significant promise in reducing the size of the required FC stack and improving the fuel economy. Hydrogen storage is a key area for future research for bus applications, where technologies such as solid state storage offer potential to improve the storage density of hydrogen. For widespread implementation, the development of the hydrogen infrastructure is vital. This includes the production of hydrogen, particularly from clean sources, the distribution of hydrogen or on-site production and purification.
\nWe wish to thank the Engineering and Physical Sciences Research Council (EPSRC) who have funded the HyFCap (Reducing the cost and prolonging the durability of hydrogen fuel cell systems by in-situ hydrogen purification and technology hybridisation) (grant number: EP/K021192/1) jointly carried out by University College London and University of Sheffield.
\nRecombinant DNA technology involves genetic engineering; cutting DNA molecules from distinct biological species and then ligating them to a vector for expression [1, 2]. The technology helps to express the desired protein in large quantity rather than extracting from bulk amounts of tissues and animal fluids. Proteins are synthesized and modified depending on their functions in an organism. As an initial step, DNA encodes protein through transcription from mRNA synthesis. Then, mRNA is converted into protein. Transcription and translation occur simultaneously in prokaryotic organisms. The conversion of mRNA to protein begins before the synthesis of the mature mRNA transcript [3]. Protein expression involves the synthesis, modification, and regulation of a particular protein in a living organism. However, bacterial systems lack human protein modifications but overexpress recombinant proteins in bulk amounts [4]. Recombinant protein expression is useful to understand the structure and function of proteins. A network of protein complex functions can be distinguished by the characterization of individual proteins function as well as interactions through recombinant protein techniques. Protein–protein and protein-ligand interactions may be highlighted by expressing interacting domains and by introducing key mutations to reveal key domains and residues, respectively. Considering the size and complexity of proteins, protein production is very efficient with vector templates using K12 bacterial systems [2, 4].
Recombinant protein production in bacterial systems is fast, easy, and highly efficient [5]. The general strategy for recombinant protein production involves transforming the cell with a DNA vector containing the open reading frame of the gene, then after subcloning to the expression system, the protein is induced in the cells. After incubating the induced cells, harvested cells are lysed for further separation. The selection of the purification system depends on the type of protein, the affinity tag of the plasmid, the isoelectric point (pI) of the protein of interest, the molecular mass of the protein, the targeted yield, and the degree of functional activity. The lysed cells are purified through column chromatography with a proper resin(s) and a convenient buffer system [6, 7]. But in practice, several steps may cause problems. These include inadequate growth of the selected bacterial host cell, the formation of inclusion bodies, protein aggregation, structural alteration, recombinant protein nonspecific interaction with cellular proteins, problems in colon systems used in purification [6, 8]. Further, as eukaryotic proteins expressed in E. coli may not perform post-translation modifications of other organism proteins, loss of function is observed. In addition, some of the proteins expressed are exposed to hard-denaturing agents or may cause collapses in structure and this often results in insolubility problems. Overexpression of recombinant proteins in bacterial systems leads to the formation of inclusion bodies. Re-folding of these proteins into their bioactive forms is cumbersome and requires a variety of agents and processes [1, 9].
First of all, the choice of the host cells to produce intact protein in the synthesis mechanism forms the mainline of the whole system. Microorganisms used in recombinant protein expression systems include bacteria and yeast. Each host has strengths and weaknesses. The organism to be selected varies depending on the particular protein, working conditions, desired yield. For example, if the desired protein has post-translational modifications, choosing a prokaryotic expression system would not be proper [10]. BL21 (DE3) and its derivatives are by far the most commonly used strains for recombinant protein synthesis. In addition, its genetics are characterized in more detail than any other microorganisms. Recent studies suggest that BL21 (DE3) gene-level research made this bacterium more important for the production of heterologous proteins. This host cell provides maximum efficiency in protein expression through inexpensive substrates, capable of rapid and high-yield growth. A modified form includes a pLysS plasmid that encodes T7 lysozyme. This lowers the background protein expression of recombinant protein but does not perturb IPTG induction. The plasmid is especially useful in toxic cases and provides an option for protein over-expression. Yeast is an alternative recombinant protein production host and provides eukaryotic post-translational modifications with high yield. Yeast growth temperature (30°C) is lower than that of bacteria (37°C) but the growth rate is much slower. Further, the transformation of plasmids to yeast is relatively difficult and the selection of transformed cells and growth conditions require special conditions [10, 11].
The expression plasmids consist of the replication origin, promoter, and multiple cloning sites. The most important issue to consider when choosing an appropriate vector is the copy number property. Because the number of copies is controlled by the replication. It is not always true to assume that the high amount of plasmid is proportional to the yield of recombinant protein expression. Because the high copy is inversely proportional to the rate of bacterial growth. In addition, this condition creates plasmid instability and creates a metabolic load. As a result protein production yield decreases [12, 13].
Prokaryotes have to adapt to the environment by responding quickly to environmental changes. E. coli cells cannot use lactose directly as a source of carbon. But they use glucose, a component of lactose. For the bacterial cell to metabolize lactose, it is necessary to take lactose into the cell and break it down into a glucose monomer. For this, it is necessary to synthesize three different enzymes in the cell [6, 14]. As with E. coli, bacteria combine genes related to the same metabolic pathways to form clusters called operons. Transcription of the genes that make up the operon start from a single promoter. The resulting transcription product consists of an mRNA molecule containing information from multiple genes. Preserved DNA sequences in the promoter region help connect the enzyme to the DNA molecule. Induction is difficult in the presence of easily metabolized carbon sources. If lactose and glucose are present in the environment, expression from the lac promoter is not fully induced until all glucose is used up. In the absence of glucose, the promoter expresses the three enzymes to break down the lactose to obtain glucose. This property is used to induce prokaryotic expression vectors through IPTG (isopropyl 1-thio-β-d-galactopyranoside); a lactose analog that binds lac repressor [14, 15]. In the commercial vectors, IPTG starts the transcription of the lac operon and eventually induces protein expression where the gene of interest is controlled by the
A resistance marker is added to the plasmid to prevent the growth of cells that do not carry plasmids. This can be achieved by using a selection marker. For example, ampicillin resistance is conferred by the
The addition of affinity tags to the plasmid (such as His Tag, glutathione-S-transferase, and cellulose-binding domain) is employed to separate a particular protein from the heterogeneous protein mixture during purification, forming disulfide bonds, increasing the solubility of the recombinant proteins and transferring them to the periplasm region. Affinity tags have a great role in separating the desired protein from cell lysate in recombinant protein purification. Affinity tags are divided into small peptide tags (amino acids) and large polypeptide tags (fusion partners) [17]. Small peptide tags are less likely to interfere when fused to the protein. In some cases, this may have negative consequences on the tertiary conformation and biological activity of the fused chimeric protein. Vectors are available that allow tags to be placed optionally at the N-terminal or C-terminal end. It is more advantageous to position a signal peptide at the N-terminal end for better secretion of the recombinant protein. At this point, it is important to know which end of the protein is embedded in the folding pattern by examining the three-dimensional structure of a particular protein, and it is necessary to place the label on the solvent-exposed end. Examples of small peptide tags are poly-His, c-Myc, and FLAG [18]. His-tagged proteins can be purified by affinity chromatography in resins containing positively charged metal ion nickel. In addition, at the end of purification, with commercial antibodies, labeled recombinant protein can be detected by western blot [17, 18, 19, 20, 21]. On the other hand, it increases the solubility of the recombinant protein produced by the addition of a non-peptide fusion partner (large polypeptide label). The most commonly used fusion labels include Thioredoxin (Trx), Ubiquitin, SUMO, Maltose binding protein (MBP), Glutathione S-transferase (GST) [17, 22]. The reason why fusion partners show properties that increase the solubility of the protein is still not fully explained. Though, MBP label has been shown to carry a small chaperone activity. The GST label has been shown to have the weakest solubility-enhancing effect among fusion partners. Trx has the most solubility-enhancing properties, but due to its size, it may cause adverse effects. In recent years, studies have shown that “Calcium-Binding Protein Fh8” tag derived from a parasite called “Fasciola hepatica” recombinantly added to proteins increases protein solubility [6, 17, 20, 21]. Studies are underway for better solubility enhancing effect of recombinant protein tags.
Even if the effective parameters are provided in the production of recombinant protein, it may not be determined exactly whether the desired protein will be eluted excessively and in active soluble form. Therefore, there are additional strategies for optimizing protein expression [7].
If the desired protein cannot be detected using sensitive techniques or is detected at a low expression rate, the problem is usually caused by a toxic effect of the heterologous protein in the cell. As a result of protein toxicity in the host cell, cells cannot proliferate at a sufficient level and show a low growth rate [7, 23]. The first measure to solve this problem should be followed before proliferating cells are induced. If the growth rate of the recombinant cell is slower than that of the strain with empty vectors, it is related to either gene toxicity or the basal expression of toxic mRNA and protein. Control of basal production is associated with the operon system.
Luria Bertani (LB), the most commonly used growth medium environment for E. coli culture, is an ideal environment for high-nutrient cell growth. When recombinant protein production cannot be replicated with the recommended mechanisms, production efficiency can be increased by increasing the volume of the targeted protein. A successful result can be achieved with adequate ventilation with rigorous shaking of the growth medium. Although LB has a high protein content, cell proliferation is partially reduced. This is due to the low carbohydrate content of LB. As a solution to this situation, increasing peptone and yeast extract provides higher cell proliferation with the addition of MgSO4, which contributes to the sonic intensity of the environment. In addition, the amount of acid released as a result of increased glucose metabolism over time exceeds the buffering capacity of LB. In case of acidification of the growth medium, 50 mM phosphate salts can be added to the environment and buffered [7, 11]. In the broth culture, as the number of cells per unit media increases, oxygen limitation occurs and changes the metabolic capacity of the cell. This prevents optimal growth and the easiest way to increase the amount of oxygen in the growth medium is to increase the speed of the shaking containers. The optimum shaking speed range is 300–400 rpm. Several anti-foaming agents can be added to the broth culture to prevent the negative effect of the foams formed by strong shaking on oxygen circulation [24].
The inclusion bodies formed in E. coli are denatured protein molecules that do not display biological activity. Dissolving, refolding, and purification protocols should be applied, respectively, to make inclusion objects functionally active and soluble. In the transfer of a foreign gene to E. coli, control of gene expression is lost. The nascent polypeptide expression depends on several factors such as osmosis, folding pattern, and pH. If expression increases, the number of unspecific hydrophobic interactions in the polypeptide chain increases. This causes instability and clustering in poly peptization. The resulting protein aggregation is called “inclusion bodies.” The main reason for the formation of clustering is due to the deterioration of the balance between protein aggregation and protein resolution [1, 25]. Therefore, a soluble recombinant protein can be obtained through strategies that eliminate the factors causing the formation of inclusion bodies. As mentioned in the “Affinity tags” section, one way to prevent the solubility problem that may occur in the expressed protein is; combining the desired protein with a fusion partner (large polypeptide tag) that acts as a solubilizer [17].
To obtain the biologically active three-dimensional structure of recombinant proteins, it is important to establish the right disulfide bonds. The formation of improper disulfide bonds causes the protein to fold incorrectly and the formation of inclusion bodies. Disulfide change reactions catalyzed by many enzymes in the Dsb family, where cysteine oxidation occurs in E. coli periplasm, form disulfide bonds in the polypeptide chain [26]. In the cytoplasm, the formation of disulfide bonds is rare because the remnants of cysteine are catalytic regions for many enzymes in the cytoplasm. The wrong disulfide bonds in these regions can cause protein inactivation, clustering, and incorrect folding. However, some strains of E. coli have conditions that trigger the formation of a disulfide bond [5].
Molecular chaperones form the heart of protein synthesis and help nascent polypeptides fold into their active structures. Some specific types of chaperones, such as ClpB, can cleave unfolded polypeptides contained in inclusion bodies. However, high levels of recombinant protein production may result in increased molecular traffic in the cytoplasm, resulting in uncontrolled protein folding control. One strategy used to solve this problem is to arrest protein expression by removing the inducer after a centrifugation step and adding a fresh medium containing chloramphenicol, the protein expression inhibitor. Thus, it allows the recruitment of molecular chaperones to enable the folding of newly synthesized recombinant polypeptides [27, 28]. One of the systems used commercially for protein folding is chaperone plasmids. This system consists of plasmids that allow overexpression of different chaperones or their combinations. Examples of these are GroES-GroEL, DNAK/DNAJ/GrpE [27]. When proteins are released from inclusion bodies, denatured with urea, and subsequently folded
Slowing the production rate of the recombinant protein reduces cellular protein concentration and protein trafficking, allowing the synthesized polypeptides to fold more smoothly. The most common method of reducing the rate of protein synthesis is to lower the incubation temperature [29]. Decreased temperature prevents the formation of aggregation due to its reduction of hydrophobic interactions. Recombinant protein synthesis occurs in the temperature range of 15–25°C. However, when working at the lower temperature range, this causes slower growth and therefore lower protein synthesis. This obstacle can be overcome with commercial products. The ArticExpress™ (Agilent Technologies) competent cells improve recombinant protein expression at low temperatures through co-expressing ortholog genes of E. coli GroEL and GroES from Oleispira Antarctica, namely Cpn60 and co-chaperone Cpn10. These chaperones work together to fold a substrate protein, and usually carry re-folding activity at 4–12°C temperature range, increasing recombinant protein yield and solubility at lower temperatures [30].
Selection of the purification methods generally uses distinct characteristics of the proteins. The distinct properties of recombinant proteins may include chemical, biological, and physical features due to differences in spatial structure and amino acid sequences. Usually, to benefit from these differences, multiple steps are required in the optimal purification process but it should be noted that each step may cause loss of product stability and/or yield, therefore the lowest number of steps are recommended overall for maximum yield. So, method selection determines the ratio of better yield to the better-purified product. Key factors that can affect the purification selection steps include the solubility of the lysate, sample size, and physicochemical properties of the target protein. The first step for purification is to analyze the protein characteristics and match them with literature reports-protocols. For example, a useful parameter in the purification process is amino acid composition. pKa and pI values can be calculated using the amino acid composition. Determination of the values helps to select column type, buffer, pH, or resin type. Once optimization of the purification is established, the method may be employed for a protein with similar sequences or motifs at least for orthologs or isoforms [31]. The characteristic features of proteins that are mainly used for purification type selection are solubility, size, charge, and specific binding affinity [32]. By using these properties, numerous techniques may be employed in protein purification. Solubility parameter can be used with “salting out” through the knowledge of proteins mostly being less soluble in high salt concentrations. And hence, this strategy can be used to separate the protein of interest. Further, dialysis can be used after salting out to remove the salt molecules [33]. Another technique that uses size difference is gel-filtration or size exclusion chromatography (SEC). A column with porous beads resin is used for this and as the sample goes through the column, beads help to separate molecules. The beads are usually 0.1 mm in diameter, so bigger molecules cannot permeate the pores but small molecules penetrate into the pores and are trapped there for a while until the molecules exit again and return to solvent. This action retards small molecules but bigger molecules travel rapidly through a void volume with buffer flow. Small molecules shielding and bigger molecules faster flow separate molecules from each other in fractions depending on their sizes. And as the molecules exit the column, bigger molecules elute first and then, smaller molecules come after.
If the net charge is criteria to be used as a separating feature, ion-exchange chromatography can be used. If the target protein is positively charged as a cationic protein, then, a negatively charged carboxymethyl-cellulose (CM-cellulose) pre-packed column/resin can be used. But if the protein is negatively charged as in anionic proteins, then positively charged diethylaminoethyl-cellulose (DEAE-cellulose) pre-packed columns/resin can be used [33]. It is also known that proteins can have high affinities for certain chemical groups. Affinity chromatography can use this feature to purify proteins and its effect is the best on proteins with affinities to highly specific molecules.
Distinct separation techniques, that is, ion exchange and gel filtration may be employed at high-pressure liquid chromatography (HPLC) with proper column selection. This technique differs from the others because the applied pressure is significantly higher and it does not rely on gravity for sample flow. However, high-pressure limits the purification of higher molecular weight proteins as the pressure denatures protein structure. For higher-molecular-weight proteins FPLC (fast-pressure liquid chromatography) is preferred to prevent pressure-dependent denaturation. FPLC is the preferred technique for protein chemists since any target protein can be separated from cellular lysate readily. And the technique provides a wide range of column options. The flexibility of this technique provides the purification of stable proteins with a high yield. Lower pressure provides advantages as well. Clogging due to lysate content and backpressure problems are less likely encountered compared to that of HPLC. The techniques may also be used with tagged proteins. Histidine tag is one of the most common ones that are used with recombinant proteins and it has a high affinity of metal ions like Ni2+ [17]. To screen if the purification steps are working, gel electrophoresis can be used. In-gel electrophoresis, proteins are separated by their mass as they go through the gel and the smaller ones move faster. As they get separated by their masses, proteins can be visualized in the gel and the gel show protein of interest among others. Another feature to separate proteins is their isoelectric point. This point represents the pH level where the protein has zero net charges. The technique that uses this property to separate proteins is called isoelectric focusing. When proteins go through a pH gradient gel, they will stop at the point where they have no net charge and get separated from the proteins with distinct isoelectric points. To get more specific results, isoelectric focusing can be coupled with SDS-PAGE (sodium dodecyl sulfate-polyacrylamide gel electrophoresis) in a technique called two-dimensional electrophoresis. In this technique, first isoelectric focusing is done as the sample goes through the gel horizontally and after proteins stop at their respective pH levels, vertical electrophoresis starts. So, the sample is separated according to the isoelectric points horizontally and by their masses vertically. The two-dimensional separation technique is employed to distinguish differences in two different states. Actually, distinct spots may be characterized by MALDI-TOF mass spectrometry.
The structure and function of a protein are essential to characterize the linkage associated between common motifs and biochemical activity [34]. These features are normally determined by NMR or X-ray crystallography techniques [35]. NMR determines dynamic structure but the technique is limited to protein molecular mass. However, an instant picture of the protein structure with a relatively higher mass can be taken by X-ray crystallography. After elucidation of information from these structure determination techniques, scientists concluded that similar sequences show similar structural patterns [36]. Then, different databases which can display protein 2 and 3-dimensional structures have been developed. Determination of protein structure is important for not only understanding the function but also important for protein experiments, such as protein purification. Proteins have alpha helixes, turns, and beta sheets as secondary structures. Beta sheet structures and the outer surface of alpha helixes of proteins can accumulate within the cellular medium or stick to each other and other proteins during aggregation.
Protein structure can be determined by bioinformatic tools such as Swiss Modeling or I-Tasser. Swiss model and I-Tasser are Protein Data Bank (PDB) dependent protein homology modeling databases. They use the known templates from PDB. Swiss Modeling is quicker than I-Tasser, however, I-Tasser produces better and more stable results. Swiss Modeling uses known sequences on the internet and generates data by comparing known structures. Both Swiss Modeling and I-Tasser have the advantage of understanding the main structure of the protein. Protein structure screening is a key factor to understanding interactions of proteins within themselves and with the environment. 3D modeled protein structures can be screened with commercially available tools like YASARA and Discovery Studio Tool. In these tools, not only protein structure is screened, but also domains of proteins can be separated, deleted and water molecules can be removed. UCSF Chimera and Autodock Tools also can be used for screening. After modeling, structures may be downloaded as PDB format and can be visualized by several programs: Discovery Studio, Autodock Vina, UCSF Chimera, etc. Interactions within the protein and secondary-tertiary structures can be obtained from these tools. All these tools work with a PDB file. There are other tools for protein structure determination and can be found at https://www.click2drug.org/. This website provides database links for distinct applications.
Protein databases play a crucial role in bioinformatics and help to find information related to their research. In this way, all biological information becomes accessible through data mining tools saving time and resources. The first step in the study of a new protein is searching databases. Without the prior knowledge from such searches, previously known protein information could be missed, or an experiment could be repeated unnecessarily. There are hundreds of useful databases that can be used in protein research. However, in this study, the pI and 3D structure of the peptide were obtained using the Swiss database and Expasy Database. The purpose of the Swiss Database is to make protein structure modeling accessible. Therefore, with this database, the 3D shape of the protein provided us with information to understand the structure of the peptide and its interactions. Additionally, Expasy Database provides information about proteomics, post-translational modification prediction, primary, secondary, and tertiary structure analysis, sequence alignment, and pI of the protein [37]. The pI of the peptide provides the pH range where that peptide has a negative charge and prepares the buffer solution accordingly. Consequently, databases have key roles in biological research, and enormous data for protein structures, functions, and sequences can be generated by these available databases. These data offer essential information about our protein research as well. Figure 1 provides the predicted structure for our research. SB#14 model indicates that the protein is formed from β-sheet structures.
Predicted structure of Sb#14. Sb#14 is a recombinant synthetic monoclonal antibody 14 used to detect spike protein of COVID-19 and used for immunodetection of the virus. SB#14 is modeled by the Swiss model to design purification steps for the TUSEB project.
Protein solubility is one of the most important protein properties and it can be defined as the protein concentration in a saturated solution that is in equilibrium with a solid phase [38]. Not only some extrinsic factors, including pH, ionic strength, temperature, and some solvent additives, can affect the protein solubility but also several intrinsic factors influence protein solubility. Moreover, the amino acids on the protein surface are the primary intrinsic factors that impact protein solubility [39]. Several studies have revealed the relationship between protein solubility and sequence-derived characteristics. Wilkinson and Harrison et al. provided a simple approach for predicting protein solubility from the sequence, which was further refined by Davis et al. [40]. The average charge, which is derived by the relative quantities of Asp, Glu, Lys, and Arg residues, and the concentration of turn-forming residues are the two parameters used in their solubility model (Asn, Gly, Pro, and Ser). In addition, Christendat et al. have demonstrated that insoluble proteins had more hydrophobic stretches (more than 20 amino acids), less glutamine (Q 4%), fewer negatively charged residues (DE 17%), and a higher percentage of aromatic amino acids (FYW >7.5%) than soluble proteins [41]. The affinity tag (His/GST) in recombinant protein purified by affinity chromatography allows the protein to be purified. However, affinity tag has been observed to alter the biological activity of the protein. Because a minor difference affects protein solubility, the choice of affinity tag at the N- or C-terminus is important when expressing a protein domain. Klock and colleagues investigated a nested collection of 2143N- and C-terminal truncations from 96 targets and found significant variance in both solubility and aggregation processes by changing just a few amino acids in a protein length [42]. Therefore, it is essential to analyze which end of the protein is hidden. Furthermore, if the three-dimensional structure is known, the tag should be kept in a solvent-accessible end. In this way, the solubility of the protein can be increased. Insoluble proteins can aggregate during the expression process. That is why the different parameters should be optimized. On the other hand, during downstream purification steps, protein aggregation can occur. In these cases, developing a suitable and optimized purification procedure for each protein is critical. Sb#14 hydrophobic nature (Figure 1) leads to solubility problems as well as aggregation. The protein sticks to larger proteins and this led to difficulties in purification.
Imidazole is one of the most widely used organic compounds in protein affinity purification processes. It is used as a competitive agent to elute the histidine-tagged proteins. High concentrated imidazole that includes protein samples should be eliminated after eluting from the nickel column by dialysis [43]. In spite of all precautions, his tagged Sb#14 sticks to other proteins and has low solubility, therefore, SEC is used for protein purification rather than affinity purification. As mentioned, SEC separates proteins according to the molecular weight of the molecule. SEC performed with Superdex 75 size-exclusion column 10/30 (GE Healthcare, Princeton, NJ, USA). Moreover, SEC (15 cm length with r, 3 cm column) used in this study separates aggregates readily. Lower molecular weight of Sb#14 provides an advantage in the purification process, recalling that larger proteins elute first. This custom SEC column was unique as the resin resolution is high while the column length is relatively lower. The choice of resin and column size helped to resolve Sb#14 from bacterial lysate in a single purification step. The peptide (MW: 12.468 g/mol, pI: 8.91) is small and prone to aggregate. Therefore, the single-step purification blocks the self-cleavage of protein domains.
The stability of the protein in various buffer compositions and pH levels with and without ligands should be determined. There are some useful websites for fold recognition that can be used to predict the protein fold (PSI-BLAST and SEARCH). Some proteins are misfolded and require the addition of a cofactor, or ligand to restore proper folding and increase stability. For instance, beta-sheets are more prone to form amyloid-like aggregates if there are other binding partners that support protein stabilization and folding [44]. If the protein has a large number of beta-sheets, aggregation may be observed. This can be explained by the tendency of sticking together at Sb#14 and leading to the formation of insoluble aggregates. Tris–HCl buffer is used to stabilize Sb# 14.
To reduce aggregation, reducing agents such as dithiothreitol (DTT) may be used and added to the buffer. DTT is called Cleland’s reagent and is used for protein reduction. However, a high concentration of DTT can reduce the nickel ion in the resin of the column. That is why the determination of the optimal concentration of DTT is essential. β-ME (Beta-mercaptoethanol) cleaves protein disulfide bonds (cystine), and TCEP (Tris phosphine hydrochloride) can also be used as reducing agents, considering longer half-life β-ME. DTT reacts easily with nickel ions whereas β-ME reacts easily with cobalt, copper ions, and other phosphate buffers [44]. A precaution is required to obtain optimal conditions.
Each protein has a pI, where the protein’s net charge is zero. Protein does not migrate at that point, and aggregation occurs [45]. On one hand, acidic proteins are likely to crystallize 0–2.5 pH units above their isoelectric point. On the other hand, basic proteins are more likely to crystallize 1.5–3 pH units below their pI. Hence, different pH values affect the protein’s stability and solubility [46]. The pI of the peptide is important for us to know the pH range where that peptide has a negative charge and to prepare the buffer solution accordingly. That is why the pH of the buffer component is one of the most critical parameters. Sb #14 has a pI value of 8.91. This value set the pH parameter (pH:7.91) of the buffer used in the purification process.
pI represents the pH level of a molecule where the net charge is zero. Amino acid composition of the protein can be used to calculate an estimated value with the help of databases [47]. If the pI is lower than the pH of a solution, protein will have a negative charge but if it is the opposite then the protein will have a positive charge. This feature can be used for purification purposes since it is a specific physicochemical parameter to distinguish between amphoteric molecules [39]. Also, it can be used to understand how solution pH can affect the protein stability in the pH range. So, buffers are used to keep proteins stable. To create an environment for protein to be stable, generally, the buffer is selected to have a pH level around the pI of the protein. If this difference between the pI of protein and pH of the solution gets larger then protein gets a greater net charge too. With this greater net charge, ionic compounds will be able to bind residues [48]. To avoid this unspecific interaction, the buffer’s pH range should be selected accordingly to the protein’s pI. And this knowledge of pH values with their effects on the proteins can be useful in the purification process. In tagged protein purification, affinity chromatography is a commonly used technique. The pH levels also affect this technique since affinity resins have their pH ranges to provide more stable links for not only the ligand and the bead but also for the tag and the ligand. While making decisions about the purification protocol, the affinity resins’ and the tags’ working pH ranges should be kept in mind to create a better environment and more stable interaction. Also choosing affinity resins and tags that have a wider range of pH that they can work may be useful for the purification of proteins.
Proteins are special structures that work with covalent and non-covalent interactions. They have cellular wide roles, including signaling, structural and metabolic processes. Their special structural features and 3D architecture determine their roles and interactions. These forms of proteins are determined by the amino acid sequences [49]. Proteins are not synthesized in their functional form. When their translation process is finished, the primary protein structure is formed. After that, they form alpha helixes and beta sheets by hydrogen bonds. Alpha helixes and beta sheets interact with each other with weak interactions and disulfide bonds and tertiary structure is formed. In some instances, the quaternary structure may be formed when tertiary structures interact and eventually in all cases functional protein forms [55]. However, in some cases, proteins can accumulate and form aggregates which may cause failure in protein purification experiments. Mostly, beta-sheets tend to interact with each other and accumulate. This event can be exampled by amyloid aggregates in Alzheimer’s disease. Recombinant protein aggregates resulted in the prevention of exposure of tags in tagged protein that causes failure in purification. Also, solubility prevents aggregate formation in proteins [50]. Protein aggregation can be prevented by adding salt to the proteins. Salt ions interact with the charged protein surface areas and prevent non-specific interactions, aggregation, and lower protein–protein interaction. However, a precaution is a must when preparing protein for binding experiments. Please note that high ionic concentration blocks ligand/protein binding experiments. As shown in Figure 2, Sb #14 is prone to aggregation and the process may be prevented/decreased through proper conditions.
Ionic strength is important for the separation of proteins from each other that can be aggregated. The strength of ions resists accumulation by preventing protein-protein interaction.
Urea dissolves the aggregated protein solutions. The efficiency of the process is increased by taking the necessary purification steps [1, 51]. Among these processes, protein dissolving and refolding steps constitute the most important steps for optimal protein activity and higher recovery. The protein precipitate is generally separated from other cellular components by low-speed centrifugation after cell lysis. Because protein aggregates are denser than cellular components, the lysate proteins are precipitated by centrifugation and then dissolved using detergents such as urea, guanidine-HCl, high concentrations of chaotropic denaturants, sodium N-lauroyl sarcosine, SDS, N-acetyl trimethyl ammonium chloride [52]. Further, additional reducing agents such as DTT, cysteine, Triton X-100, β-ME are used to dissolve inclusion bodies. These agents retain cysteine residues, minimizing the formation of false and unnatural disulfide bonds in the protein solution. Metal-containing oxidation of cysteine is prevented by using chelating agents such as EDTA in dissolution buffers [44, 52]. By removing the soluble protein content, removing the chaotropic reagents, and diluting them directly into the renaturation buffer, the recombinant proteins are folded back into their native form [44]. Protein collapse is a higher-order reaction while protein folding is a lower-order reaction. Therefore, the aggregation rate is higher than the folding rate. Due to the kinetic competition that occurs, the increase in protein concentration decreases the folding efficiency of the protein. For accurate and efficient folding kinetics, the preferred protein concentration is used in the range of 10–50 μg.ml−1 [1, 53]. As explained in the section of ‘Disulfide bond formation’, recombinant proteins with multiple disulfide bonds in their structure tend to be in a correct folding process in the presence of both oxidizing and reducing agents for the formation of these bonds. The simplest way for oxidation is to oxidize the protein with air in the presence of a metal catalyst. Another common oxidation option is the addition of thiol agents containing compounds such as glutathione, cysteine, cysteamine to the protein mixture. The most commonly used thiol reagents are reduced/oxidized glutathione (GSH-GSSH), cysteine/cystine, DTT/GSSH, cysteamine compounds [1, 36]. There are also low-molecular-weight additives that help refolding process. There are studies on the use of additives such as acetone, DMSO, short-chain alcohols, PEG in the bioactive protein process. In addition, it has been observed that L-arginine/HCl reduces aggregation on protein. The 0.4–1 M arginine used in the studies also increases the protein folding efficiency by reducing the aggregation in the recombinant protein solution. This feature of arginine has been attributed to the interaction of the guanidino structure in its structure with tryptophan residues in proteins [44, 52, 53, 54, 55]. Sb #14 was also treated with DTT but when overexpressed, the protein has solubility problems. The structure is highly prone to aggregation and solubility may be increased upon co-expressing chaperones/Heat Shock Proteins or yeast systems seem proper for preventing aggregation. Yet, this may not solve the problem but mutational studies may provide more soluble and stable structures.
Protein purification depends on several factors: resin type, solvent, ionic strength, pH, protein structural tendency to aggregation, buffer systems, protein structure, ligand if any, column dimension. For each factor, problems may be encountered. To eliminate these problems and decide on protein purification protocol, protein structural properties must be examined initially. Tandem purification steps may also increase the purification yield. However, self-cleavage of certain proteins or oxidation that may distort the protein function leads to problems. Therefore, several distinct protocols may be tested before purifying the targeted protein with high efficiency and functionality. Sb#14 structure mainly consists of β-sheets and overexpressing this petit protein lead aggregation. Solubility is another problem in the cellular milieu as Sb#14 hydrophobic nature interacts with other proteins in the lysate. Therefore, proper solvent selection (phosphate buffer) and adjusting the pH (1 unit lower than pI, 7.91) provide soluble protein. Further, we take advantage of the protein’s lower molecular weight and employed a convenient resin (Superdex 75-separates 3000–70,000 molecular weights, most of the lysate elutes before Sb#14) and custom size column (15 cm length with r: 3 cm-lower pressure yet increase resolution). The purification was performed with high yield by AKTA go FPLC system. Additionally, co-expressing heat shock proteins with this type of protein may help in folding and dissolving aggregates. All these conditions must be tested for individual proteins for optimum purification yield.
Prof. Dr. Yusuf TUTAR acknowledges grant from TUSEB (Project # 8970-220-CV-01) and infrastructure grant from the University of Health Sciences-Turkey (Project #2017-041). Sb#14 is from Addgene (#153522).
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After finishing his P. hD degree in 1992, he served in the Industry as a Scientific Officer and continued his academic career as a visiting scholar for a number of educational institutions. In 1996 he joined National University of Science & Technology Pakistan (NUST) as an Associate Professor; NUST is one of the top few universities in Pakistan. In 1999 he joined an International Company Lineo Inc, Canada as Manager Compiler Group, where he headed the group for developing Compiler Tool Chain and Porting of Operating Systems for the BLACKfin processor. The processor development was a joint venture by Intel and Analog Devices. In 2002 Lineo Inc., was taken over by another company, so he joined Aalborg University Denmark as an Assistant Professor.\nProfessor Akbar has truly a multi-disciplined career and he continued his legacy and making progress in many areas of his interests both in teaching and research. 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He is an academic staff member of the Department of Reproduction and Artificial Insemination, Selçuk University, Turkey. He manages several studies on sperms and embryos and is an editorial board member for several international journals. His studies include sperm cryobiology, in vitro fertilization, and embryo production in animals.",institutionString:"Selçuk University, Faculty of Veterinary Medicine",institution:null},{id:"90846",title:"Prof.",name:"Yusuf",middleName:null,surname:"Bozkurt",slug:"yusuf-bozkurt",fullName:"Yusuf Bozkurt",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/90846/images/system/90846.jpg",biography:"Yusuf Bozkurt has a BSc, MSc, and Ph.D. from Ankara University, Turkey. He is currently a Professor of Biotechnology of Reproduction in the field of Aquaculture, İskenderun Technical University, Turkey. His research interests include reproductive biology and biotechnology with an emphasis on cryo-conservation. He is on the editorial board of several international peer-reviewed journals and has published many papers. Additionally, he has participated in many international and national congresses, seminars, and workshops with oral and poster presentations. He is an active member of many local and international organizations.",institutionString:"İskenderun Technical University",institution:{name:"İskenderun Technical University",country:{name:"Turkey"}}},{id:"61139",title:"Dr.",name:"Sergey",middleName:null,surname:"Tkachev",slug:"sergey-tkachev",fullName:"Sergey Tkachev",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/61139/images/system/61139.png",biography:"Dr. Sergey Tkachev is a senior research scientist at the Institute of Fundamental Medicine and Biology, Kazan Federal University, Russia, and at the Institute of Chemical Biology and Fundamental Medicine SB RAS, Novosibirsk, Russia. He received his Ph.D. in Molecular Biology with his thesis “Genetic variability of the tick-borne encephalitis virus in natural foci of Novosibirsk city and its suburbs.” His primary field is molecular virology with research emphasis on vector-borne viruses, especially tick-borne encephalitis virus, Kemerovo virus and Omsk hemorrhagic fever virus, rabies virus, molecular genetics, biology, and epidemiology of virus pathogens.",institutionString:"Russian Academy of Sciences",institution:{name:"Russian Academy of Sciences",country:{name:"Russia"}}},{id:"310962",title:"Dr.",name:"Amlan",middleName:"Kumar",surname:"Patra",slug:"amlan-patra",fullName:"Amlan Patra",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/310962/images/system/310962.jpg",biography:"Amlan K. Patra, FRSB, obtained a Ph.D. in Animal Nutrition from Indian Veterinary Research Institute, India, in 2002. He is currently an associate professor at West Bengal University of Animal and Fishery Sciences. He has more than twenty years of research and teaching experience. He held previous positions at the American Institute for Goat Research, The Ohio State University, Columbus, USA, and Free University of Berlin, Germany. His research focuses on animal nutrition, particularly ruminants and poultry nutrition, gastrointestinal electrophysiology, meta-analysis and modeling in nutrition, and livestock–environment interaction. He has authored around 175 articles in journals, book chapters, and proceedings. Dr. Patra serves on the editorial boards of several reputed journals.",institutionString:null,institution:{name:"West Bengal University of Animal and Fishery Sciences",country:{name:"India"}}},{id:"53998",title:"Prof.",name:"László",middleName:null,surname:"Babinszky",slug:"laszlo-babinszky",fullName:"László Babinszky",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/53998/images/system/53998.png",biography:"László Babinszky is Professor Emeritus, Department of Animal Nutrition Physiology, University of Debrecen, Hungary. He has also worked in the Department of Animal Nutrition, University of Wageningen, Netherlands; the Institute for Livestock Feeding and Nutrition (IVVO), Lelystad, Netherlands; the Agricultural University of Vienna (BOKU); the Institute for Animal Breeding and Nutrition, Austria; and the Oscar Kellner Research Institute for Animal Nutrition, Rostock, Germany. In 1992, Dr. Babinszky obtained a Ph.D. in Animal Nutrition from the University of Wageningen. His main research areas are swine and poultry nutrition. He has authored more than 300 publications (papers, book chapters) and edited four books and fourteen international conference proceedings.",institutionString:"University of Debrecen",institution:{name:"University of Debrecen",country:{name:"Hungary"}}},{id:"201830",title:"Dr.",name:"Fernando",middleName:"Sanchez",surname:"Davila",slug:"fernando-davila",fullName:"Fernando Davila",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/201830/images/5017_n.jpg",biography:"I am a professor at UANL since 1988. My research lines are the development of reproductive techniques in small ruminants. We also conducted research on sexual and social behavior in males.\nI am Mexican and study my professional career as an engineer in agriculture and animal science at UANL. Then take a masters degree in science in Germany (Animal breeding). Take a doctorate in animal science at the UANL.",institutionString:null,institution:{name:"Universidad Autónoma de Nuevo León",country:{name:"Mexico"}}},{id:"309250",title:"Dr.",name:"Miguel",middleName:null,surname:"Quaresma",slug:"miguel-quaresma",fullName:"Miguel Quaresma",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/309250/images/9059_n.jpg",biography:"Miguel Nuno Pinheiro Quaresma was born on May 26, 1974 in Dili, Timor Island. He is married with two children: a boy and a girl, and he is a resident in Vila Real, Portugal. He graduated in Veterinary Medicine in August 1998 and obtained his Ph.D. degree in Veterinary Sciences -Clinical Area in February 2015, both from the University of Trás-os-Montes e Alto Douro. He is currently enrolled in the Alternative Residency of the European College of Animal Reproduction. He works as a Senior Clinician at the Veterinary Teaching Hospital of UTAD (HVUTAD) with a role in clinical activity in the area of livestock and equine species as well as to support teaching and research in related areas. He teaches as an Invited Professor in Reproduction Medicine I and II of the Master\\'s in Veterinary Medicine degree at UTAD. Currently, he holds the position of Chairman of the Portuguese Buiatrics Association. He is a member of the Consultive Group on Production Animals of the OMV. He has 19 publications in indexed international journals (ISIS), as well as over 60 publications and oral presentations in both Portuguese and international journals and congresses.",institutionString:"University of Trás-os-Montes and Alto Douro",institution:{name:"University of Trás-os-Montes and Alto Douro",country:{name:"Portugal"}}},{id:"38652",title:"Prof.",name:"Rita",middleName:null,surname:"Payan-Carreira",slug:"rita-payan-carreira",fullName:"Rita Payan-Carreira",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRiFPQA0/Profile_Picture_1614601496313",biography:"Rita Payan Carreira earned her Veterinary Degree from the Faculty of Veterinary Medicine in Lisbon, Portugal, in 1985. She obtained her Ph.D. in Veterinary Sciences from the University of Trás-os-Montes e Alto Douro, Portugal. After almost 32 years of teaching at the University of Trás-os-Montes and Alto Douro, she recently moved to the University of Évora, Department of Veterinary Medicine, where she teaches in the field of Animal Reproduction and Clinics. Her primary research areas include the molecular markers of the endometrial cycle and the embryo–maternal interaction, including oxidative stress and the reproductive physiology and disorders of sexual development, besides the molecular determinants of male and female fertility. She often supervises students preparing their master's or doctoral theses. She is also a frequent referee for various journals.",institutionString:null,institution:{name:"University of Évora",country:{name:"Portugal"}}},{id:"283019",title:"Dr.",name:"Oudessa",middleName:null,surname:"Kerro Dego",slug:"oudessa-kerro-dego",fullName:"Oudessa Kerro Dego",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/283019/images/system/283019.png",biography:"Dr. Kerro Dego is a veterinary microbiologist with training in veterinary medicine, microbiology, and anatomic pathology. Dr. Kerro Dego is an assistant professor of dairy health in the department of animal science, the University of Tennessee, Institute of Agriculture, Knoxville, Tennessee. He received his D.V.M. (1997), M.S. (2002), and Ph.D. (2008) degrees in Veterinary Medicine, Animal Pathology and Veterinary Microbiology from College of Veterinary Medicine, Addis Ababa University, Ethiopia; College of Veterinary Medicine, Utrecht University, the Netherlands and Western College of Veterinary Medicine, University of Saskatchewan, Canada respectively. He did his Postdoctoral training in microbial pathogenesis (2009 - 2015) in the Department of Animal Science, the University of Tennessee, Institute of Agriculture, Knoxville, Tennessee. Dr. Kerro Dego’s research focuses on the prevention and control of infectious diseases of farm animals, particularly mastitis, improving dairy food safety, and mitigation of antimicrobial resistance. Dr. Kerro Dego has extensive experience in studying the pathogenesis of bacterial infections, identification of virulence factors, and vaccine development and efficacy testing against major bacterial mastitis pathogens. Dr. Kerro Dego conducted numerous controlled experimental and field vaccine efficacy studies, vaccination, and evaluation of immunological responses in several species of animals, including rodents (mice) and large animals (bovine and ovine).",institutionString:"University of Tennessee at Knoxville",institution:{name:"University of Tennessee at Knoxville",country:{name:"United States of America"}}},{id:"251314",title:"Dr.",name:"Juan Carlos",middleName:null,surname:"Gardón",slug:"juan-carlos-gardon",fullName:"Juan Carlos Gardón",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/251314/images/system/251314.jpeg",biography:"Juan Carlos Gardón Poggi received University degree from the Faculty of Agrarian Science in Argentina, in 1983. Also he received Masters Degree and PhD from Córdoba University, Spain. He is currently a Professor at the Catholic University of Valencia San Vicente Mártir, at the Department of Medicine and Animal Surgery. He teaches diverse courses in the field of Animal Reproduction and he is the Director of the Veterinary Farm. He also participates in academic postgraduate activities at the Veterinary Faculty of Murcia University, Spain. His research areas include animal physiology, physiology and biotechnology of reproduction either in males or females, the study of gametes under in vitro conditions and the use of ultrasound as a complement to physiological studies and development of applied biotechnologies. Routinely, he supervises students preparing their doctoral, master thesis or final degree projects.",institutionString:"Catholic University of Valencia San Vicente Mártir, Spain",institution:null},{id:"125292",title:"Dr.",name:"Katy",middleName:null,surname:"Satué Ambrojo",slug:"katy-satue-ambrojo",fullName:"Katy Satué Ambrojo",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/125292/images/system/125292.jpeg",biography:"Katy Satué Ambrojo received her Veterinary Medicine degree, Master degree in Equine Technology and doctorate in Veterinary Medicine from the Faculty of Veterinary, CEU-Cardenal Herrera University in Valencia, Spain. She is a Full Professor at the Department of Medicine and Animal Surgery at the same University. She developed her research activity in the field of Endocrinology, Hematology, Biochemistry and Immunology of horses. She is a scientific reviewer of several international journals : American Journal of Obstetrics and Gynecology, Comparative Clinical Pathology, Veterinary Clinical Pathology, Journal of Equine Veterinary Science, Reproduction in Domestic Animals, Research Veterinary Science, Brazilian Journal of Medical and Biological Research, Livestock Production Science and Theriogenology. Since 2014, she has been the Head of the Clinical Analysis Laboratory of the Hospital Clínico Veterinario from the Faculty of Veterinary, CEU-Cardenal Herrera University.",institutionString:"CEU-Cardenal Herrera University",institution:{name:"CEU Cardinal Herrera University",country:{name:"Spain"}}},{id:"309529",title:"Dr.",name:"Albert",middleName:null,surname:"Rizvanov",slug:"albert-rizvanov",fullName:"Albert Rizvanov",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/309529/images/9189_n.jpg",biography:'Albert A. Rizvanov is a Professor and Director of the Center for Precision and Regenerative Medicine at the Institute of Fundamental Medicine and Biology, Kazan Federal University (KFU), Russia. He is the Head of the Center of Excellence “Regenerative Medicine” and Vice-Director of Strategic Academic Unit \\"Translational 7P Medicine\\". Albert completed his Ph.D. at the University of Nevada, Reno, USA and Dr.Sci. at KFU. He is a corresponding member of the Tatarstan Academy of Sciences, Russian Federation. Albert is an author of more than 300 peer-reviewed journal articles and 22 patents. He has supervised 11 Ph.D. and 2 Dr.Sci. dissertations. Albert is the Head of the Dissertation Committee on Biochemistry, Microbiology, and Genetics at KFU.\nORCID https://orcid.org/0000-0002-9427-5739\nWebsite https://kpfu.ru/Albert.Rizvanov?p_lang=2',institutionString:"Kazan Federal University",institution:{name:"Kazan Federal University",country:{name:"Russia"}}},{id:"210551",title:"Dr.",name:"Arbab",middleName:null,surname:"Sikandar",slug:"arbab-sikandar",fullName:"Arbab Sikandar",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/210551/images/system/210551.jpg",biography:"Dr. Arbab Sikandar, PhD, M. Phil, DVM was born on April 05, 1981. He is currently working at the College of Veterinary & Animal Sciences as an Assistant Professor. He previously worked as a lecturer at the same University. \nHe is a Member/Secretory of Ethics committee (No. CVAS-9377 dated 18-04-18), Member of the QEC committee CVAS, Jhang (Regr/Gen/69/873, dated 26-10-2017), Member, Board of studies of Department of Basic Sciences (No. CVAS. 2851 Dated. 12-04-13, and No. CVAS, 9024 dated 20/11/17), Member of Academic Committee, CVAS, Jhang (No. CVAS/2004, Dated, 25-08-12), Member of the technical committee (No. CVAS/ 4085, dated 20,03, 2010 till 2016).\n\nDr. Arbab Sikandar contributed in five days hands-on-training on Histopathology at the Department of Pathology, UVAS from 12-16 June 2017. He received a Certificate of appreciation for contributions for Popularization of Science and Technology in the Society on 17-11-15. He was the resource person in the lecture series- ‘scientific writing’ at the Department of Anatomy and Histology, UVAS, Lahore on 29th October 2015. He won a full fellowship as a principal candidate for the year 2015 in the field of Agriculture, EICA, Egypt with ref. to the Notification No. 12(11) ACS/Egypt/2014 from 10 July 2015 to 25th September 2015.; he received a grant of Rs. 55000/- as research incentives from Director, Advanced Studies and Research, UVAS, Lahore upon publications of research papers in IF Journals (DR/215, dated 19-5-2014.. He obtained his PhD by winning a HEC Pakistan indigenous Scholarship, ‘Ph.D. fellowship for 5000 scholars – Phase II’ (2av1-147), 17-6/HEC/HRD/IS-II/12, November 15, 2012. \n\nDr. Sikandar is a member of numerous societies: Registered Veterinary Medical Practitioner (life member) and Registered Veterinary Medical Faculty of Pakistan Veterinary Medical Council. The Registration code of PVMC is RVMP/4298 and RVMF/ 0102.; Life member of the University of Veterinary and Animal Sciences, Lahore, Alumni Association with S# 664, dated: 6-4-12. ; Member 'Vets Care Organization Pakistan” with Reference No. VCO-605-149, dated 05-04-06. :Member 'Vet Crescent” (Society of Animal Health and Production), UVAS, Lahore.",institutionString:"University of Veterinary & Animal Science",institution:{name:"University of Veterinary and Animal Sciences",country:{name:"Pakistan"}}},{id:"311663",title:"Dr.",name:"Prasanna",middleName:null,surname:"Pal",slug:"prasanna-pal",fullName:"Prasanna Pal",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/311663/images/13261_n.jpg",biography:null,institutionString:null,institution:{name:"National Dairy Research Institute",country:{name:"India"}}},{id:"202192",title:"Dr.",name:"Catrin",middleName:null,surname:"Rutland",slug:"catrin-rutland",fullName:"Catrin Rutland",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/202192/images/system/202192.png",biography:"Catrin Rutland is an Associate Professor of Anatomy and Developmental Genetics at the University of Nottingham, UK. She obtained a BSc from the University of Derby, England, a master’s degree from Technische Universität München, Germany, and a Ph.D. from the University of Nottingham. She undertook a post-doctoral research fellowship in the School of Medicine before accepting tenure in Veterinary Medicine and Science. Dr. Rutland also obtained an MMedSci (Medical Education) and a Postgraduate Certificate in Higher Education (PGCHE). She is the author of more than sixty peer-reviewed journal articles, twelve books/book chapters, and more than 100 research abstracts in cardiovascular biology and oncology. She is a board member of the European Association of Veterinary Anatomists, Fellow of the Anatomical Society, and Senior Fellow of the Higher Education Academy. Dr. Rutland has also written popular science books for the public. https://orcid.org/0000-0002-2009-4898. www.nottingham.ac.uk/vet/people/catrin.rutland",institutionString:null,institution:{name:"University of Nottingham",country:{name:"United Kingdom"}}},{id:"283315",title:"Prof.",name:"Samir",middleName:null,surname:"El-Gendy",slug:"samir-el-gendy",fullName:"Samir El-Gendy",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRduYQAS/Profile_Picture_1606215849748",biography:"Samir El-Gendy is a Professor of anatomy and embryology at the faculty of veterinary medicine, Alexandria University, Egypt. Samir obtained his PhD in veterinary science in 2007 from the faculty of veterinary medicine, Alexandria University and has been a professor since 2017. Samir is an author on 24 articles at Scopus and 12 articles within local journals and 2 books/book chapters. His research focuses on applied anatomy, imaging techniques and computed tomography. Samir worked as a member of different local projects on E-learning and he is a board member of the African Association of Veterinary Anatomists and of anatomy societies and as an associated author at local and international journals. Orcid: https://orcid.org/0000-0002-6180-389X",institutionString:null,institution:{name:"Alexandria University",country:{name:"Egypt"}}},{id:"246149",title:"Dr.",name:"Valentina",middleName:null,surname:"Kubale",slug:"valentina-kubale",fullName:"Valentina Kubale",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/246149/images/system/246149.jpg",biography:"Valentina Kubale is Associate Professor of Veterinary Medicine at the Veterinary Faculty, University of Ljubljana, Slovenia. Since graduating from the Veterinary faculty she obtained her PhD in 2007, performed collaboration with the Department of Pharmacology, University of Copenhagen, Denmark. She continued as a post-doctoral fellow at the University of Copenhagen with a Lundbeck foundation fellowship. She is the editor of three books and author/coauthor of 23 articles in peer-reviewed scientific journals, 16 book chapters, and 68 communications at scientific congresses. Since 2008 she has been the Editor Assistant for the Slovenian Veterinary Research journal. She is a member of Slovenian Biochemical Society, The Endocrine Society, European Association of Veterinary Anatomists and Society for Laboratory Animals, where she is board member.",institutionString:"University of Ljubljana",institution:{name:"University of Ljubljana",country:{name:"Slovenia"}}},{id:"258334",title:"Dr.",name:"Carlos Eduardo",middleName:null,surname:"Fonseca-Alves",slug:"carlos-eduardo-fonseca-alves",fullName:"Carlos Eduardo Fonseca-Alves",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/258334/images/system/258334.jpg",biography:"Dr. Fonseca-Alves earned his DVM from Federal University of Goias – UFG in 2008. He completed an internship in small animal internal medicine at UPIS university in 2011, earned his MSc in 2013 and PhD in 2015 both in Veterinary Medicine at Sao Paulo State University – UNESP. Dr. Fonseca-Alves currently serves as an Assistant Professor at Paulista University – UNIP teaching small animal internal medicine.",institutionString:null,institution:{name:"Universidade Paulista",country:{name:"Brazil"}}},{id:"245306",title:"Dr.",name:"María Luz",middleName:null,surname:"Garcia Pardo",slug:"maria-luz-garcia-pardo",fullName:"María Luz Garcia Pardo",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/245306/images/system/245306.png",biography:"María de la Luz García Pardo is an agricultural engineer from Universitat Politècnica de València, Spain. She has a Ph.D. in Animal Genetics. Currently, she is a lecturer at the Agrofood Technology Department of Miguel Hernández University, Spain. Her research is focused on genetics and reproduction in rabbits. The major goal of her research is the genetics of litter size through novel methods such as selection by the environmental sensibility of litter size, with forays into the field of animal welfare by analysing the impact on the susceptibility to diseases and stress of the does. Details of her publications can be found at https://orcid.org/0000-0001-9504-8290.",institutionString:null,institution:{name:"Miguel Hernandez University",country:{name:"Spain"}}},{id:"350704",title:"M.Sc.",name:"Camila",middleName:"Silva Costa",surname:"Ferreira",slug:"camila-ferreira",fullName:"Camila Ferreira",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/350704/images/17280_n.jpg",biography:"Graduated in Veterinary Medicine at the Fluminense Federal University, specialist in Equine Reproduction at the Brazilian Veterinary Institute (IBVET) and Master in Clinical Veterinary Medicine and Animal Reproduction at the Fluminense Federal University. She has experience in analyzing zootechnical indices in dairy cattle and organizing events related to Veterinary Medicine through extension grants. I have experience in the field of diagnostic imaging and animal reproduction in veterinary medicine through monitoring and scientific initiation scholarships. I worked at the Equus Central Reproduction Equine located in Santo Antônio de Jesus – BA in the 2016/2017 breeding season. I am currently a doctoral student with a scholarship from CAPES of the Postgraduate Program in Veterinary Medicine (Pathology and Clinical Sciences) at the Federal Rural University of Rio de Janeiro (UFRRJ) with a research project with an emphasis on equine endometritis.",institutionString:null,institution:null},{id:"41319",title:"Prof.",name:"Lung-Kwang",middleName:null,surname:"Pan",slug:"lung-kwang-pan",fullName:"Lung-Kwang Pan",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/41319/images/84_n.jpg",biography:null,institutionString:null,institution:null},{id:"201721",title:"Dr.",name:"Beatrice",middleName:null,surname:"Funiciello",slug:"beatrice-funiciello",fullName:"Beatrice Funiciello",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/201721/images/11089_n.jpg",biography:"Graduated from the University of Milan in 2011, my post-graduate education included CertAVP modules mainly on equines (dermatology and internal medicine) and a few on small animal (dermatology and anaesthesia) at the University of Liverpool. After a general CertAVP (2015) I gained the designated Certificate in Veterinary Dermatology (2017) after taking the synoptic examination and then applied for the RCVS ADvanced Practitioner status. After that, I completed the Postgraduate Diploma in Veterinary Professional Studies at the University of Liverpool (2018). My main area of work is cross-species veterinary dermatology.",institutionString:null,institution:null},{id:"291226",title:"Dr.",name:"Monica",middleName:null,surname:"Cassel",slug:"monica-cassel",fullName:"Monica Cassel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/291226/images/8232_n.jpg",biography:'Degree in Biological Sciences at the Federal University of Mato Grosso with scholarship for Scientific Initiation by FAPEMAT (2008/1) and CNPq (2008/2-2009/2): Project \\"Histological evidence of reproductive activity in lizards of the Manso region, Chapada dos Guimarães, Mato Grosso, Brazil\\". Master\\\'s degree in Ecology and Biodiversity Conservation at Federal University of Mato Grosso with a scholarship by CAPES/REUNI program: Project \\"Reproductive biology of Melanorivulus punctatus\\". PhD\\\'s degree in Science (Cell and Tissue Biology Area) \n at University of Sao Paulo with scholarship granted by FAPESP; Project \\"Development of morphofunctional changes in ovary of Astyanax altiparanae Garutti & Britski, 2000 (Teleostei, Characidae)\\". She has experience in Reproduction of vertebrates and Morphology, with emphasis in Cellular Biology and Histology. She is currently a teacher in the medium / technical level courses at IFMT-Alta Floresta, as well as in the Bachelor\\\'s degree in Animal Science and in the Bachelor\\\'s degree in Business.',institutionString:null,institution:null},{id:"442807",title:"Dr.",name:"Busani",middleName:null,surname:"Moyo",slug:"busani-moyo",fullName:"Busani Moyo",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Gwanda State University",country:{name:"Zimbabwe"}}},{id:"423023",title:"Dr.",name:"Yosra",middleName:null,surname:"Soltan",slug:"yosra-soltan",fullName:"Yosra Soltan",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Alexandria University",country:{name:"Egypt"}}},{id:"349788",title:"Dr.",name:"Florencia Nery",middleName:null,surname:"Sompie",slug:"florencia-nery-sompie",fullName:"Florencia Nery Sompie",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Sam Ratulangi University",country:{name:"Indonesia"}}},{id:"208123",title:"Dr.",name:"Mari-Carmen",middleName:null,surname:"Uribe",slug:"mari-carmen-uribe",fullName:"Mari-Carmen Uribe",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"National Autonomous University of Mexico",country:{name:"Mexico"}}},{id:"345713",title:"Dr.",name:"Csaba",middleName:null,surname:"Szabó",slug:"csaba-szabo",fullName:"Csaba Szabó",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Debrecen",country:{name:"Hungary"}}},{id:"345719",title:"Mrs.",name:"Márta",middleName:null,surname:"Horváth",slug:"marta-horvath",fullName:"Márta Horváth",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Debrecen",country:{name:"Hungary"}}},{id:"420151",title:"Prof.",name:"Novirman",middleName:null,surname:"Jamarun",slug:"novirman-jamarun",fullName:"Novirman Jamarun",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Andalas University",country:{name:"Indonesia"}}}]}},subseries:{item:{id:"11",type:"subseries",title:"Cell Physiology",keywords:"Neurodevelopment and Neurodevelopmental Disease, Free Radicals, Tumor Metastasis, Antioxidants, Essential Fatty Acids, Melatonin, Lipid Peroxidation Products and Aging Physiology",scope:"\r\n\tThe integration of tissues and organs throughout the mammalian body, as well as the expression, structure, and function of molecular and cellular components, is essential for modern physiology. The following concerns will be addressed in this Cell Physiology subject, which will consider all organ systems (e.g., brain, heart, lung, liver; gut, kidney, eye) and their interactions: (1) Neurodevelopment and Neurodevelopmental Disease (2) Free Radicals (3) Tumor Metastasis (4) Antioxidants (5) Essential Fatty Acids (6) Melatonin and (7) Lipid Peroxidation Products and Aging Physiology.
",coverUrl:"https://cdn.intechopen.com/series_topics/covers/11.jpg",hasOnlineFirst:!0,hasPublishedBooks:!0,annualVolume:11407,editor:{id:"133493",title:"Prof.",name:"Angel",middleName:null,surname:"Catala",slug:"angel-catala",fullName:"Angel Catala",profilePictureURL:"https://mts.intechopen.com/storage/users/133493/images/3091_n.jpg",biography:"Prof. Dr. Angel Catalá \r\nShort Biography Angel Catalá was born in Rodeo (San Juan, Argentina). He studied \r\nchemistry at the Universidad Nacional de La Plata, Argentina, where received aPh.D. degree in chemistry (Biological Branch) in 1965. From\r\n1964 to 1974, he worked as Assistant in Biochemistry at the School of MedicineUniversidad Nacional de La Plata, Argentina. From 1974 to 1976, he was a Fellowof the National Institutes of Health (NIH) at the University of Connecticut, Health Center, USA. From 1985 to 2004, he served as a Full Professor oBiochemistry at the Universidad Nacional de La Plata, Argentina. He is Member ofthe National Research Council (CONICET), Argentina, and Argentine Society foBiochemistry and Molecular Biology (SAIB). His laboratory has been interested for manyears in the lipid peroxidation of biological membranes from various tissues and different species. Professor Catalá has directed twelve doctoral theses, publishedover 100 papers in peer reviewed journals, several chapters in books andtwelve edited books. Angel Catalá received awards at the 40th InternationaConference Biochemistry of Lipids 1999: Dijon (France). W inner of the Bimbo PanAmerican Nutrition, Food Science and Technology Award 2006 and 2012, South AmericaHuman Nutrition, Professional Category. 2006 award in pharmacology, Bernardo\r\nHoussay, in recognition of his meritorious works of research. Angel Catalá belongto the Editorial Board of Journal of lipids, International Review of Biophysical ChemistryFrontiers in Membrane Physiology and Biophysics, World Journal oExperimental Medicine and Biochemistry Research International, W orld Journal oBiological Chemistry, Oxidative Medicine and Cellular Longevity, Diabetes and thePancreas, International Journal of Chronic Diseases & Therapy, International Journal oNutrition, Co-Editor of The Open Biology Journal.",institutionString:null,institution:{name:"National University of La Plata",institutionURL:null,country:{name:"Argentina"}}},editorTwo:null,editorThree:null,series:{id:"10",title:"Physiology",doi:"10.5772/intechopen.72796",issn:"2631-8261"},editorialBoard:[{id:"186048",title:"Prof.",name:"Ines",middleName:null,surname:"Drenjančević",slug:"ines-drenjancevic",fullName:"Ines Drenjančević",profilePictureURL:"https://mts.intechopen.com/storage/users/186048/images/5818_n.jpg",institutionString:null,institution:{name:"University of Osijek",institutionURL:null,country:{name:"Croatia"}}},{id:"187859",title:"Prof.",name:"Kusal",middleName:"K.",surname:"Das",slug:"kusal-das",fullName:"Kusal Das",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSBDeQAO/Profile_Picture_1623411145568",institutionString:"BLDE (Deemed to be University), India",institution:null},{id:"79615",title:"Dr.",name:"Robson",middleName:null,surname:"Faria",slug:"robson-faria",fullName:"Robson Faria",profilePictureURL:"https://mts.intechopen.com/storage/users/79615/images/system/79615.png",institutionString:null,institution:{name:"Oswaldo Cruz Foundation",institutionURL:null,country:{name:"Brazil"}}},{id:"84459",title:"Prof.",name:"Valerie",middleName:null,surname:"Chappe",slug:"valerie-chappe",fullName:"Valerie Chappe",profilePictureURL:"https://mts.intechopen.com/storage/users/84459/images/system/84459.jpg",institutionString:null,institution:{name:"Dalhousie University",institutionURL:null,country:{name:"Canada"}}}]},onlineFirstChapters:{paginationCount:20,paginationItems:[{id:"80964",title:"Upper Airway Expansion in Disabled Children",doi:"10.5772/intechopen.102830",signatures:"David Andrade, Joana Andrade, Maria-João Palha, Cristina Areias, Paula Macedo, Ana Norton, Miguel Palha, Lurdes Morais, Dóris Rocha Ruiz and Sônia Groisman",slug:"upper-airway-expansion-in-disabled-children",totalDownloads:35,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Oral Health Care - An Important Issue of the Modern Society",coverURL:"https://cdn.intechopen.com/books/images_new/10827.jpg",subseries:{id:"1",title:"Oral Health"}}},{id:"80839",title:"Herbs and Oral Health",doi:"10.5772/intechopen.103715",signatures:"Zuhair S. 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