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dc.creatorSalar García, María J.es
dc.creatorBernal, Vicentees
dc.creatorPastor, José M.es
dc.creatorSalvador de Lara, Manueles
dc.creatorArgandoña Bertrán, Montserrates
dc.creatorNieto Gutiérrez, Joaquín Josées
dc.creatorVargas Macías, Carmenes
dc.date.accessioned2017-05-17T11:44:39Z
dc.date.available2017-05-17T11:44:39Z
dc.date.issued2017
dc.identifier.citationSalar García, M.J., Bernal, V., Pastor, J.M., Salvador de Lara, M., Argandoña Bertrán, M., Nieto Rodríguez, J.J. y Vargas Macías, C. (2017). Understanding the interplay of carbon and nitrogen supply for ectoines production and metabolic overflow in high density cultures of Chromohalobacter salexigens. Microbial Cell Factories, 16 (1), 1-12.
dc.identifier.issn1475-2859es
dc.identifier.urihttp://hdl.handle.net/11441/59966
dc.description.abstractBackground The halophilic bacterium Chromohalobacter salexigens has been proposed as promising cell factory for the production of the compatible solutes ectoine and hydroxyectoine. This bacterium has evolved metabolic adaptations to efficiently grow under high salt concentrations by accumulating ectoines as compatible solutes. However, metabolic overflow, which is a major drawback for the efficient conversion of biological feedstocks, occurs as a result of metabolic unbalances during growth and ectoines production. Optimal production of ectoines is conditioned by the interplay of carbon and nitrogen metabolisms. In this work, we set out to determine how nitrogen supply affects the production of ectoines. Results Chromohalobacter salexigens was challenged to grow in media with unbalanced carbon/nitrogen ratio. In C. salexigens, overflow metabolism and ectoines production are a function of medium composition. At low ammonium conditions, the growth rate decreased importantly, up to 80%. Shifts in overflow metabolism were observed when changing the C/N ratio in the culture medium. 13C-NMR analysis of ectoines labelling revealed a high metabolic rigidity, with almost constant flux ratios in all conditions assayed. Unbalanced C/N ratio led to pyruvate accumulation, especially upon N-limitation. Analysis of an ect − mutant demonstrated the link between metabolic overflow and ectoine biosynthesis. Under non ectoine synthesizing conditions, glucose uptake and metabolic overflow decreased importantly. Finally, in fed-batch cultures, biomass yield was affected by the feeding scheme chosen. High growth (up to 42.4 g L−1) and volumetric ectoine yields (up to 4.21 g L−1) were obtained by minimizing metabolite overflow and nutrient accumulation in high density cultures in a low nitrogen fed-batch culture. Moreover, the yield coefficient calculated for the transformation of glucose into biomass was 30% higher in fed-batch than in the batch culture, demonstrating that the metabolic efficiency of C. salexigens can be improved by careful design of culture feeding schemes. Conclusions Metabolic shifts observed at low ammonium concentrations were explained by a shift in the energy required for nitrogen assimilation. Carbon-limited fed-batch cultures with reduced ammonium supply were the best conditions for cultivation of C. salexigens, supporting high density growth and maintaining high ectoines production.es
dc.description.sponsorshipEspaña, Ministerio de Ciencia e Innovación BIO2011-29233-C02-01es
dc.description.sponsorshipEspaña, Ministerio de Economía y Competitividad BIO2014-54411-C2-1-Res
dc.formatapplication/pdfes
dc.language.isoenges
dc.publisherBioMed Centrales
dc.relation.ispartofMicrobial Cell Factories, 16 (1), 1-12.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectC. salexigenses
dc.subjectEctoineses
dc.subjectCarbon overflowes
dc.subjectHalophilismes
dc.subjectFed-batches
dc.subjectNitrogen assimilationes
dc.titleUnderstanding the interplay of carbon and nitrogen supply for ectoines production and metabolic overflow in high density cultures of Chromohalobacter salexigenses
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Microbiología y Parasitologíaes
dc.relation.projectIDBIO2011-29233-C02-01es
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO/BIO2014-54411-C2-1-Res
dc.relation.publisherversionhttp://dx.doi.org/10.1186/s12934-017-0643-7.es
dc.identifier.doi10.1186/s12934-017-0643-7es
dc.journaltitleMicrobial Cell Factorieses
dc.publication.volumen16es
dc.publication.issue1es
dc.publication.initialPage1es
dc.publication.endPage12es
dc.contributor.funderMinisterio de Ciencia e Innovación (MICIN). España
dc.contributor.funderMinisterio de Economía y Competitividad (MINECO). España

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