Metabolic engineering of Escherichia coli for alpha-farnesene production

Cited 187 time in scopus
Metadata Downloads

Full metadata record

DC FieldValueLanguage
dc.contributor.authorC Wang-
dc.contributor.authorS H Yoon-
dc.contributor.authorH J Jang-
dc.contributor.authorY R Chung-
dc.contributor.authorJ Y Kim-
dc.contributor.authorEui Sung Choi-
dc.contributor.authorS W Kim-
dc.date.accessioned2017-04-19T09:25:58Z-
dc.date.available2017-04-19T09:25:58Z-
dc.date.issued2011-
dc.identifier.issn1096-7176-
dc.identifier.uri10.1016/j.ymben.2011.08.001ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/10417-
dc.description.abstractSesquiterpenes are important materials in pharmaceuticals and industry. Metabolic engineering has been successfully used to produce these valuable compounds in microbial hosts. However, the microbial potential of sesquiterpene production is limited by the poor heterologous expression of plant sesquiterpene synthases and the deficient FPP precursor supply. In this study, we engineered E. coli to produce α-farnesene using a codon-optimized α-farnesene synthase and an exogenous MVA pathway. Codon optimization of α-farnesene synthase improved both the synthase expression and α-farnesene production. Augmentation of the metabolic flux for FPP synthesis conferred a 1.6- to 48.0-fold increase in α-farnesene production. An additional increase in α-farnesene production was achieved by the protein fusion of FPP synthase and α-farnesene synthase. The engineered E. coli strain was able to produce 380.0. mg/L of α-farnesene, which is an approximately 317-fold increase over the initial production of 1.2. mg/L.-
dc.publisherElsevier-
dc.titleMetabolic engineering of Escherichia coli for alpha-farnesene production-
dc.title.alternativeMetabolic engineering of Escherichia coli for alpha-farnesene production-
dc.typeArticle-
dc.citation.titleMetabolic Engineering-
dc.citation.number6-
dc.citation.endPage655-
dc.citation.startPage648-
dc.citation.volume13-
dc.contributor.affiliatedAuthorEui Sung Choi-
dc.contributor.alternativeNameWang-
dc.contributor.alternativeName윤상활-
dc.contributor.alternativeName장희정-
dc.contributor.alternativeName정영련-
dc.contributor.alternativeName김재연-
dc.contributor.alternativeName최의성-
dc.contributor.alternativeName김선원-
dc.identifier.bibliographicCitationMetabolic Engineering, vol. 13, no. 6, pp. 648-655-
dc.identifier.doi10.1016/j.ymben.2011.08.001-
dc.subject.keywordα-Farnesene-
dc.subject.keywordCodon optimization-
dc.subject.keywordFPP synthesis-
dc.subject.keywordMevalonate pathway-
dc.subject.keywordProtein fusion-
dc.subject.localα-Farnesene-
dc.subject.localcodon optimization-
dc.subject.localCodon optimization-
dc.subject.localFPP synthesis-
dc.subject.localMevalonate pathway-
dc.subject.localmevalonate pathway-
dc.subject.localMevalonate Pathway-
dc.subject.localProtein fusion-
dc.description.journalClassY-
Appears in Collections:
Division of Bio Technology Innovation > BioProcess Engineering Center > 1. Journal Articles
Files in This Item:
  • There are no files associated with this item.


Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.