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Identification of Factors Regulating Escherichia coli 2,3-Butanediol Production by Continuous Culture and Metabolic Flux Analysis

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dc.contributor.authorLu, Mingshou-
dc.contributor.authorLee, Soojin-
dc.contributor.authorKim, Borim-
dc.contributor.authorPark, Changhun-
dc.contributor.authorOh, Minkyu-
dc.contributor.authorPark, Kyungmoon-
dc.contributor.authorLee, Sang Yup-
dc.contributor.authorLee, Jinwon-
dc.date.accessioned2021-12-02T04:43:16Z-
dc.date.available2021-12-02T04:43:16Z-
dc.date.created2021-11-29-
dc.date.issued2012-05-
dc.identifier.issn1017-7825-
dc.identifier.urihttps://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/18963-
dc.description.abstract2,3-Butanediol (2,3-BDO) is an organic compound with a wide range of industrial applications. Although Escherichia call is often used for the production of organic compounds, the wild-type E. coli does not contain two essential genes in the 2,3-BDO biosynthesis pathway, and cannot ferment 2,3-BDO. Therefore, a 2,3-BDO biosynthesis mutant strain of Escherichia coli was constructed and cultured. To determine the optimum culture factors for 2,3-BDO production, experiments were conducted under different culture environments ranging from strongly acidic to neutral pH. The extracellular metabolite profiles were obtained using high-performance liquid chromatography (HPLC), and the intracellular metabolite profiles were analyzed by ultra-performance liquid chromatography and quadruple time-of-flight mass spectrometry (UPLC/Q-TOF-MS). Metabolic flux analysis (MFA) was used to integrate these profiles. The metabolite profiles showed that 2,3-BDO production favors an acidic environment (pH 5), whereas cell mass favors a neutral environment. Furthermore, when the pH of the culture fell below 5, both the cell growth and 2,3-BDO production were inhibited.-
dc.language영어-
dc.language.isoen-
dc.publisherKOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY-
dc.subject1,3-PROPANEDIOL-
dc.subjectDISTRIBUTIONS-
dc.subjectFERMENTATION-
dc.subjectENTEROBACTER-
dc.subjectKLEBSIELLA-
dc.subjectACETOIN-
dc.subjectSTATE-
dc.titleIdentification of Factors Regulating Escherichia coli 2,3-Butanediol Production by Continuous Culture and Metabolic Flux Analysis-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, Kyungmoon-
dc.identifier.doi10.4014/jmb.1112.12018-
dc.identifier.scopusid2-s2.0-84862096503-
dc.identifier.wosid000304683100013-
dc.identifier.bibliographicCitationJOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, v.22, no.5, pp.659 - 667-
dc.relation.isPartOfJOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY-
dc.citation.titleJOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY-
dc.citation.volume22-
dc.citation.number5-
dc.citation.startPage659-
dc.citation.endPage667-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001662569-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.subject.keywordPlus1,3-PROPANEDIOL-
dc.subject.keywordPlusDISTRIBUTIONS-
dc.subject.keywordPlusFERMENTATION-
dc.subject.keywordPlusENTEROBACTER-
dc.subject.keywordPlusKLEBSIELLA-
dc.subject.keywordPlusACETOIN-
dc.subject.keywordPlusSTATE-
dc.subject.keywordAuthor2,3-Butanediol fermentation-
dc.subject.keywordAuthorcontinuous culture-
dc.subject.keywordAuthorpH influence-
dc.subject.keywordAuthormetabolic flux analysis-
dc.subject.keywordAuthorintracellular metabolic measurements-
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