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dc.contributor.authorKumar, Kanhaiya
dc.contributor.authorVenkatraman, Vishwesh
dc.contributor.authorBruheim, Per
dc.date.accessioned2022-12-06T08:12:24Z
dc.date.available2022-12-06T08:12:24Z
dc.date.created2021-03-11T12:56:31Z
dc.date.issued2021
dc.identifier.citationMicrobial Cell Factories. 2021, 20, .en_US
dc.identifier.issn1475-2859
dc.identifier.urihttps://hdl.handle.net/11250/3035978
dc.description.abstractBackground Saccharomyces cerevisiae is a well-known popular model system for basic biological studies and serves as a host organism for the heterologous production of commercially interesting small molecules and proteins. The central metabolism is at the core to provide building blocks and energy to support growth and survival in normal situations as well as during exogenous stresses and forced heterologous protein production. Here, we present a comprehensive study of intracellular central metabolite pool profiling when growing S. cerevisiae on different carbon sources in batch cultivations and at different growth rates in nutrient-limited glucose chemostats. The latest versions of absolute quantitative mass spectrometry-based metabolite profiling methodology were applied to cover glycolytic and pentose phosphate pathway metabolites, tricarboxylic acid cycle (TCA), complete amino acid, and deoxy-/nucleoside phosphate pools. Results Glutamate, glutamine, alanine, and citrate were the four most abundant metabolites for most conditions tested. The amino acid is the dominant metabolite class even though a marked relative reduction compared to the other metabolite classes was observed for nitrogen and phosphate limited chemostats. Interestingly, glycolytic and pentose phosphate pathway (PPP) metabolites display the largest variation among the cultivation conditions while the nucleoside phosphate pools are more stable and vary within a closer concentration window. The overall trends for glucose and nitrogen-limited chemostats were increased metabolite pools with the increasing growth rate. Next, comparing the chosen chemostat reference growth rate (0.12 h−1, approximate one-fourth of maximal unlimited growth rate) illuminates an interesting pattern: almost all pools are lower in nitrogen and phosphate limited conditions compared to glucose limitation, except for the TCA metabolites citrate, isocitrate and α-ketoglutarate. Conclusions This study provides new knowledge-how the central metabolism is adapting to various cultivations conditions and growth rates which is essential for expanding our understanding of cellular metabolism and the development of improved phenotypes in metabolic engineering.en_US
dc.language.isoengen_US
dc.publisherBioMed Centralen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleAdaptation of central metabolite pools to variations in growth rate and cultivation conditions in Saccharomyces cerevisiaeen_US
dc.title.alternativeAdaptation of central metabolite pools to variations in growth rate and cultivation conditions in Saccharomyces cerevisiaeen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber16en_US
dc.source.volume20en_US
dc.source.journalMicrobial Cell Factoriesen_US
dc.identifier.doi10.1186/s12934-021-01557-8
dc.identifier.cristin1897289
dc.relation.projectNorges forskningsråd: 237165en_US
dc.relation.projectNorges forskningsråd: 248885en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal