Serial adaptive laboratory evolution enhances mixed carbon metabolic capacity of Escherichia coli

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dc.contributor.authorKim, Kangsanko
dc.contributor.authorChoe, Donghuiko
dc.contributor.authorKang, Minjeongko
dc.contributor.authorCho, SangHyeokko
dc.contributor.authorCho, Suhyungko
dc.contributor.authorJeong, Ki Junko
dc.contributor.authorPalsson, Bernhardko
dc.contributor.authorCho, Byung-Kwanko
dc.date.accessioned2024-06-10T06:00:19Z-
dc.date.available2024-06-10T06:00:19Z-
dc.date.created2024-06-10-
dc.date.created2024-06-10-
dc.date.issued2024-05-
dc.identifier.citationMETABOLIC ENGINEERING, v.83, pp.160 - 171-
dc.identifier.issn1096-7176-
dc.identifier.urihttp://hdl.handle.net/10203/319706-
dc.description.abstractMicrobes have inherent capacities for utilizing various carbon sources, however they often exhibit sub-par fitness due to low metabolic efficiency. To test whether a bacterial strain can optimally utilize multiple carbon sources, Escherichia coli was serially evolved in L -lactate and glycerol. This yielded two end -point strains that evolved first in L -lactate then in glycerol, and vice versa. The end -point strains displayed a universal growth advantage on single and a mixture of adaptive carbon sources, enabled by a concerted action of carbon source-specialists and generalist mutants. The combination of just four variants of glpK , ppsA , ydcI , and rph-pyrE , accounted for more than 80% of end -point strain fitness. In addition, machine learning analysis revealed a coordinated activity of transcriptional regulators imparting condition-specific regulation of gene expression. The effectiveness of the serial adaptive laboratory evolution (ALE) scheme in bioproduction applications was assessed under single and mixed-carbon culture conditions, in which serial ALE strain exhibited superior productivity of acetoin compared to ancestral strains. Together, systems-level analysis elucidated the molecular basis of serial evolution, which hold potential utility in bioproduction applications.-
dc.languageEnglish-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleSerial adaptive laboratory evolution enhances mixed carbon metabolic capacity of Escherichia coli-
dc.typeArticle-
dc.identifier.wosid001233253100001-
dc.identifier.scopusid2-s2.0-85190758106-
dc.type.rimsART-
dc.citation.volume83-
dc.citation.beginningpage160-
dc.citation.endingpage171-
dc.citation.publicationnameMETABOLIC ENGINEERING-
dc.identifier.doi10.1016/j.ymben.2024.04.004-
dc.contributor.localauthorJeong, Ki Jun-
dc.contributor.localauthorCho, Byung-Kwan-
dc.contributor.nonIdAuthorChoe, Donghui-
dc.contributor.nonIdAuthorPalsson, Bernhard-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorMixed-carbon-
dc.subject.keywordAuthorSystems biology-
dc.subject.keywordAuthorAdaptive laboratory evolution-
dc.subject.keywordAuthorBioproduction-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusK-12 MG1655-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusMUTATIONS-
dc.subject.keywordPlusGLYCEROL-
dc.subject.keywordPlusMESO-2,3-BUTANEDIOL-
dc.subject.keywordPlusREPRESSION-
dc.subject.keywordPlusBACTERIA-
dc.subject.keywordPlusMUTANTS-
dc.subject.keywordPlusACETOIN-
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CBE-Journal Papers(저널논문)BS-Journal Papers(저널논문)
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