Production of D-ribose by metabolically engineered Escherichia coli = 대사공학적으로 조작된 대장균으로부터 라이보스 생산

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dc.contributor.authorH C Park-
dc.contributor.authorY J Kim-
dc.contributor.authorC W Lee-
dc.contributor.authorY T Rho-
dc.contributor.authorJ Kang-
dc.contributor.authorDae-Hee Lee-
dc.contributor.authorY J Seong-
dc.contributor.authorY C Park-
dc.contributor.authorD Lee-
dc.contributor.authorS G Kim-
dc.date.accessioned2017-08-29-
dc.date.available2017-08-29-
dc.date.issued2017-
dc.identifier.issn0032-9592-
dc.identifier.uri10.1016/j.procbio.2016.10.001ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/16986-
dc.description.abstractEscherichia coli was metabolically engineered for the production of D-ribose, a functional five-carbon sugar, from xylose. For the accumulation of D-ribose, two genes of transketolase catalyzing the conversion of D-ribose-5-phosphate to sedoheptulose-7-phosphate in pentose phosphate pathway were disrupted to create a transketolase-deficient E. coli SGK013. In batch fermentation, E. coli SGK013 grew by utilizing glucose and then started to produce D-ribose from xylose after glucose depletion. E. coli SGK013 produced 0.75g/L of D-ribose, which was identical to the standard D-ribose as confirmed by HPLC and LC/MS analyses. To improve D-ribose production, the ptsG gene encoding the glucose-specific IICB component was disrupted additionally, resulting in the construction of E. coli SGK015. The carbon catabolite repression-negative E. coli SGK015 utilized xylose and glucose simultaneously and produced up to 3.75g/L of D-ribose, which is a 5-fold improvement compared to that of E. coli SGK013.-
dc.publisherElsevier-
dc.titleProduction of D-ribose by metabolically engineered Escherichia coli = 대사공학적으로 조작된 대장균으로부터 라이보스 생산-
dc.title.alternativeProduction of D-ribose by metabolically engineered Escherichia coli-
dc.typeArticle-
dc.citation.titleProcess Biochemistry-
dc.citation.number0-
dc.citation.endPage77-
dc.citation.startPage73-
dc.citation.volume52-
dc.contributor.affiliatedAuthorDae-Hee Lee-
dc.contributor.alternativeName박해철-
dc.contributor.alternativeName김윤정-
dc.contributor.alternativeName이창완-
dc.contributor.alternativeName노용택-
dc.contributor.alternativeName강정우-
dc.contributor.alternativeName이대희-
dc.contributor.alternativeName성영제-
dc.contributor.alternativeName박용철-
dc.contributor.alternativeName이대상-
dc.contributor.alternativeName김성건-
dc.identifier.bibliographicCitationProcess Biochemistry, vol. 52, pp. 73-77-
dc.identifier.doi10.1016/j.procbio.2016.10.001-
dc.subject.keywordCatabolite repression-
dc.subject.keywordD-Ribose-
dc.subject.keywordEscherichia coli-
dc.subject.keywordTransketolase-
dc.subject.keywordXylose-
dc.subject.localcatabolite repression-
dc.subject.localCatabolite repression-
dc.subject.localD-Ribose-
dc.subject.localEscherichia coli.-
dc.subject.localescherichia coli-
dc.subject.localEscherichia Coli-
dc.subject.localEscherichia coli-
dc.subject.localE.coli-
dc.subject.localescherichia coil-
dc.subject.localE. coli-
dc.subject.localE. Coli-
dc.subject.localTransketolase-
dc.subject.localXylose-
dc.subject.localxylose-
dc.description.journalClassY-
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Synthetic Biology and Bioengineering Research Institute > Synthetic Biology Research Center > 1. Journal Articles
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