Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/37910

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dc.contributor.authorSargo, Cíntia R .por
dc.contributor.authorCampani, Gilsonpor
dc.contributor.authorSilva, Gabriel G.por
dc.contributor.authorGiordano, Roberto C.por
dc.contributor.authorSilva, Adilson J. dapor
dc.contributor.authorZangirolami, Teresa C.por
dc.contributor.authorCorreia, Daniela M.por
dc.contributor.authorFerreira, Eugénio C.por
dc.contributor.authorRocha, I.por
dc.date.accessioned2015-11-03T10:56:49Z-
dc.date.available2015-11-03T10:56:49Z-
dc.date.issued2015-09-
dc.identifier.citationSargo, C.; Campani Junior, Gilson; Silva, Gabriel G.; Correia, Daniela M.; Giordano, Roberto C.; Ferreira, E. C.; Rocha, I.; Silva, A.; Zangirolami, Teresa C., Salmonella typhimurium and Escherichia coli dissimilarity: Closely related bacteria with distinct metabolic profiles. Biotechnology Progress, 31(5), 1217-1225, 2015por
dc.identifier.issn8756-7938por
dc.identifier.urihttps://hdl.handle.net/1822/37910-
dc.description.abstractLive attenuated strains of Salmonella typhimurium have been extensively investigated as vaccines for a number of infectious diseases. However, there is still little information available concerning aspects of their metabolism. S. typhimurium and Escherichia coli show a high degree of similarity in terms of their genome contents and metabolic networks. However, this work presents experimental evidence showing that significant differences exist in their abilities to direct carbon fluxes to biomass and energy production. It is important to study the metabolism of Salmonella in order to elucidate the formation of acetate and other metabolites involved in optimizing the production of biomass, essential for the development of recombinant vaccines. The metabolism of Salmonella under aerobic conditions was assessed using continuous cultures performed at dilution rates ranging from 0.1 to 0.67 h1, with glucose as main substrate. Acetate assimilation and glucose metabolism under anaerobic conditions were also investigated using batch cultures. Chemostat cultivations showed deviation of carbon towards acetate formation, starting at dilution rates above 0.1 h1. This differed from previous findings for E. coli, where acetate accumulation was only detected at dilution rates exceeding 0.4 h1, and was due to the lower rate of acetate assimilation by S. typhimurium under aerobic conditions. Under anaerobic conditions, both microorganisms mainly produced ethanol, acetate, and formate. A genome-scale metabolic model, reconstructed for Salmonella based on an E. coli model, provided a poor description of the mixed fermentation pattern observed during Salmonella cultures, reinforcing the different patterns of carbon utilization exhibited by these closely related bacteria. This article is protected by copyright. All rights reserved.por
dc.description.sponsorshipSpecial thanks to Amadeus Azevedo for the HPLC analyses and technical assistance. The authors acknowledge the national funding received from CNPq (Conselho Nacional de Desenvolvimento Cientifico e Tecnologico, Brazil), the international cooperation project CAPES-FCT (Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior/Brazil-Fundacao para a Ciencia e a Tecnologia/Portugal-Process 315/11), CAPES (Atracao de Jovens Talentos-Process 064922/2014-01) and to Fundacao para a Ciencia e Tecnologia the strategic funding of UID/BIO/04469/2013 unit.por
dc.language.isoengpor
dc.publisherAmerican Chemical Societypor
dc.rightsopenAccesspor
dc.subjectSalmonella typhimuriumpor
dc.subjectAerobic/anaerobic conditionspor
dc.subjectExtracellular metabolomicspor
dc.subjectaerobicpor
dc.subjectanaerobic conditionspor
dc.titleSalmonella typhimurium and Escherichia coli dissimilarity: closely related bacteria with distinct metabolic profilespor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttp://onlinelibrary.wiley.com/journal/10.1021/(ISSN)1520-6033por
dc.commentsCEB22181por
sdum.publicationstatuspublishedpor
oaire.citationStartPage1217por
oaire.citationEndPage1225por
oaire.citationIssue5por
oaire.citationConferencePlaceUnited States-
oaire.citationTitleBiotechnology progresspor
oaire.citationVolume31por
dc.date.updated2015-11-02T21:37:53Z-
dc.identifier.eissn1520-6033-
dc.identifier.doi10.1002/btpr.2128por
dc.identifier.pmid26097206por
dc.subject.wosScience & Technologypor
sdum.journalBiotechnology progresspor
Aparece nas coleções:CEB - Publicações em Revistas/Séries Internacionais / Publications in International Journals/Series

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