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Increased 2,3-butanediol production by changing codon usages in Escherichia coli

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dc.contributor.authorPark, Seo-Young-
dc.contributor.authorKim, Borim-
dc.contributor.authorLee, Soojin-
dc.contributor.authorOh, Minkyu-
dc.contributor.authorWon, Jong-In-
dc.contributor.authorLee, Jinwon-
dc.date.accessioned2021-11-11T02:42:54Z-
dc.date.available2021-11-11T02:42:54Z-
dc.date.created2021-10-25-
dc.date.issued2014-09-
dc.identifier.issn0885-4513-
dc.identifier.urihttps://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/16610-
dc.description.abstractThe natural microorganism Escherichia coli without modification is not suitable for the efficient production of 2,3-butanediol (2,3-BD) on an industrial scale because of its poor metabolic performance. Metabolic capacities of E. coli have been improved to produce 2,3-BD efficiently, the performance of which is possible for producing such a product. Codon optimization with the ribosome-binding site for the efficient production of target genes (budA and budC) was achieved by molecular engineering, which allowed the metabolic engineering to proceed to the next level. As a result, comparing the productivity in 26H, where the amount of p18COR was 1.04g/L and that of p18WTR was 0.41g/L, represents an approximate 60.6% increase in the productivity of the p18WTR with codon optimization. In other words, p18COR was 2.54-fold greater than p18WTR in the production of 2,3-BD. (C) 2014 International Union of Biochemistry and Molecular Biology, Inc.-
dc.language영어-
dc.language.isoen-
dc.publisherWILEY-BLACKWELL-
dc.subjectALPHA-CYCLODEXTRIN GLYCOSYLTRANSFERASE-
dc.subjectPROTEIN-SYNTHESIS-
dc.subjectMESO-2,3-BUTANEDIOL-
dc.subjectOPTIMIZATION-
dc.subjectSTATE-
dc.subjectRNA-
dc.titleIncreased 2,3-butanediol production by changing codon usages in Escherichia coli-
dc.typeArticle-
dc.contributor.affiliatedAuthorWon, Jong-In-
dc.identifier.doi10.1002/bab.1216-
dc.identifier.scopusid2-s2.0-84923868558-
dc.identifier.wosid000344174600006-
dc.identifier.bibliographicCitationBIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, v.61, no.5, pp.535 - 540-
dc.relation.isPartOfBIOTECHNOLOGY AND APPLIED BIOCHEMISTRY-
dc.citation.titleBIOTECHNOLOGY AND APPLIED BIOCHEMISTRY-
dc.citation.volume61-
dc.citation.number5-
dc.citation.startPage535-
dc.citation.endPage540-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.subject.keywordPlusALPHA-CYCLODEXTRIN GLYCOSYLTRANSFERASE-
dc.subject.keywordPlusPROTEIN-SYNTHESIS-
dc.subject.keywordPlusMESO-2,3-BUTANEDIOL-
dc.subject.keywordPlusOPTIMIZATION-
dc.subject.keywordPlusSTATE-
dc.subject.keywordPlusRNA-
dc.subject.keywordAuthorEscherichia coli-
dc.subject.keywordAuthorcodon optimization-
dc.subject.keywordAuthorribosome-binding site-
dc.subject.keywordAuthor2-
dc.subject.keywordAuthor3-butanediol-
dc.subject.keywordAuthoracetolactate decarboxylase-
dc.subject.keywordAuthoracetoin reductase-
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