High-level recombinant production of squalene using selected Saccharomyces cerevisiae strains

Cited 56 time in scopus
Metadata Downloads

Full metadata record

DC FieldValueLanguage
dc.contributor.authorJong Yun Han-
dc.contributor.authorSung-Hwa Seo-
dc.contributor.authorJae Myeong Song-
dc.contributor.authorHong-Weon Lee-
dc.contributor.authorEui Sung Choi-
dc.date.accessioned2018-04-19T05:19:09Z-
dc.date.available2018-04-19T05:19:09Z-
dc.date.issued2018-
dc.identifier.issn0169-4146-
dc.identifier.uri10.1007/s10295-018-2018-4ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/17774-
dc.description.abstractFor recombinant production of squalene, which is a triterpenoid compound with increasing industrial applications, in microorganisms generally recognized as safe, we screened Saccharomyces cerevisiae strains to determine their suitability. A strong strain dependence was observed in squalene productivity among Saccharomyces cerevisiae strains upon overexpression of genes important for isoprenoid biosynthesis. In particular, a high level of squalene production (400 ± 45 mg/L) was obtained in shake flasks with the Y2805 strain overexpressing genes encoding a bacterial farnesyl diphosphate synthase (ispA) and a truncated form of hydroxyl-3-methylglutaryl-CoA reductase (tHMG1). Partial inhibition of squalene epoxidase by terbinafine further increased squalene production by up to 1.9-fold (756 ± 36 mg/L). Furthermore, squalene production of 2011 ± 75 or 1026 ± 37 mg/L was obtained from 5-L fed-batch fermentations in the presence or absence of terbinafine supplementation, respectively. These results suggest that the Y2805 strain has potential as a new alternative source of squalene production-
dc.publisherSpringer-
dc.titleHigh-level recombinant production of squalene using selected Saccharomyces cerevisiae strains-
dc.title.alternativeHigh-level recombinant production of squalene using selected Saccharomyces cerevisiae strains-
dc.typeArticle-
dc.citation.titleJournal of Industrial Microbiology & Biotechnology-
dc.citation.number4-
dc.citation.endPage251-
dc.citation.startPage239-
dc.citation.volume45-
dc.contributor.affiliatedAuthorJong Yun Han-
dc.contributor.affiliatedAuthorSung-Hwa Seo-
dc.contributor.affiliatedAuthorJae Myeong Song-
dc.contributor.affiliatedAuthorHong-Weon Lee-
dc.contributor.affiliatedAuthorEui Sung Choi-
dc.contributor.alternativeName한종윤-
dc.contributor.alternativeName서성화-
dc.contributor.alternativeName송재명-
dc.contributor.alternativeName이홍원-
dc.contributor.alternativeName최의성-
dc.identifier.bibliographicCitationJournal of Industrial Microbiology & Biotechnology, vol. 45, no. 4, pp. 239-251-
dc.identifier.doi10.1007/s10295-018-2018-4-
dc.subject.keywordFarnesyl diphosphate synthase-
dc.subject.keywordHMG-CoA reductase-
dc.subject.keywordMetabolic engineering-
dc.subject.keywordSaccharomyces cerevisiae-
dc.subject.keywordSqualene-
dc.subject.localFarnesyl diphosphate synthase-
dc.subject.localHMG-CoA reductase-
dc.subject.localMetabolic Engineering-
dc.subject.localMetabolic engineering-
dc.subject.localmetabolic engineering-
dc.subject.localSaccharomyces cerevisiae-
dc.subject.localsaccharomyces cerevisiae-
dc.subject.localSqualene-
dc.description.journalClassY-
Appears in Collections:
Division of Bio Technology Innovation > BioProcess Engineering Center > 1. Journal Articles
Division of Bio Technology Innovation > 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.