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

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dc.contributor.authorLu, Mingshouko
dc.contributor.authorLee, Soojinko
dc.contributor.authorKim, Borimko
dc.contributor.authorPark, Changhunko
dc.contributor.authorOh, Minkyuko
dc.contributor.authorPark, Kyungmoonko
dc.contributor.authorLee, Sang Yupko
dc.contributor.authorLee, Jinwonko
dc.date.accessioned2013-03-13T01:08:38Z-
dc.date.available2013-03-13T01:08:38Z-
dc.date.created2012-08-20-
dc.date.created2012-08-20-
dc.date.created2012-08-20-
dc.date.issued2012-05-
dc.identifier.citationJOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, v.22, no.5, pp.659 - 667-
dc.identifier.issn1017-7825-
dc.identifier.urihttp://hdl.handle.net/10203/104069-
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. coil 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 coil 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.languageEnglish-
dc.publisherKOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY-
dc.titleIdentification of Factors Regulating Escherichia coli 2,3-Butanediol Production by Continuous Culture and Metabolic Flux Analysis-
dc.typeArticle-
dc.identifier.wosid000304683100013-
dc.identifier.scopusid2-s2.0-84862096503-
dc.type.rimsART-
dc.citation.volume22-
dc.citation.issue5-
dc.citation.beginningpage659-
dc.citation.endingpage667-
dc.citation.publicationnameJOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY-
dc.identifier.doi10.4014/jmb.1112.12018-
dc.contributor.localauthorLee, Sang Yup-
dc.contributor.nonIdAuthorLu, Mingshou-
dc.contributor.nonIdAuthorLee, Soojin-
dc.contributor.nonIdAuthorKim, Borim-
dc.contributor.nonIdAuthorPark, Changhun-
dc.contributor.nonIdAuthorOh, Minkyu-
dc.contributor.nonIdAuthorPark, Kyungmoon-
dc.contributor.nonIdAuthorLee, Jinwon-
dc.type.journalArticleArticle-
dc.subject.keywordAuthor2,3-Butanediol fermentation-
dc.subject.keywordAuthorcontinuous culture-
dc.subject.keywordAuthorpH influence-
dc.subject.keywordAuthormetabolic flux analysis-
dc.subject.keywordAuthorintracellular metabolic measurements-
dc.subject.keywordPlus1,3-PROPANEDIOL-
dc.subject.keywordPlusDISTRIBUTIONS-
dc.subject.keywordPlusFERMENTATION-
dc.subject.keywordPlusENTEROBACTER-
dc.subject.keywordPlusKLEBSIELLA-
dc.subject.keywordPlusACETOIN-
dc.subject.keywordPlusSTATE-
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