DC Field | Value | Language |
---|---|---|
dc.contributor.author | Jong Yun Han | - |
dc.contributor.author | Sung-Hwa Seo | - |
dc.contributor.author | Jae Myeong Song | - |
dc.contributor.author | Hong-Weon Lee | - |
dc.contributor.author | Eui Sung Choi | - |
dc.date.accessioned | 2018-04-19T05:19:09Z | - |
dc.date.available | 2018-04-19T05:19:09Z | - |
dc.date.issued | 2018 | - |
dc.identifier.issn | 0169-4146 | - |
dc.identifier.uri | 10.1007/s10295-018-2018-4 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/17774 | - |
dc.description.abstract | For 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.publisher | Springer | - |
dc.title | High-level recombinant production of squalene using selected Saccharomyces cerevisiae strains | - |
dc.title.alternative | High-level recombinant production of squalene using selected Saccharomyces cerevisiae strains | - |
dc.type | Article | - |
dc.citation.title | Journal of Industrial Microbiology & Biotechnology | - |
dc.citation.number | 4 | - |
dc.citation.endPage | 251 | - |
dc.citation.startPage | 239 | - |
dc.citation.volume | 45 | - |
dc.contributor.affiliatedAuthor | Jong Yun Han | - |
dc.contributor.affiliatedAuthor | Sung-Hwa Seo | - |
dc.contributor.affiliatedAuthor | Jae Myeong Song | - |
dc.contributor.affiliatedAuthor | Hong-Weon Lee | - |
dc.contributor.affiliatedAuthor | Eui Sung Choi | - |
dc.contributor.alternativeName | 한종윤 | - |
dc.contributor.alternativeName | 서성화 | - |
dc.contributor.alternativeName | 송재명 | - |
dc.contributor.alternativeName | 이홍원 | - |
dc.contributor.alternativeName | 최의성 | - |
dc.identifier.bibliographicCitation | Journal of Industrial Microbiology & Biotechnology, vol. 45, no. 4, pp. 239-251 | - |
dc.identifier.doi | 10.1007/s10295-018-2018-4 | - |
dc.subject.keyword | Farnesyl diphosphate synthase | - |
dc.subject.keyword | HMG-CoA reductase | - |
dc.subject.keyword | Metabolic engineering | - |
dc.subject.keyword | Saccharomyces cerevisiae | - |
dc.subject.keyword | Squalene | - |
dc.subject.local | Farnesyl diphosphate synthase | - |
dc.subject.local | HMG-CoA reductase | - |
dc.subject.local | Metabolic Engineering | - |
dc.subject.local | Metabolic engineering | - |
dc.subject.local | metabolic engineering | - |
dc.subject.local | Saccharomyces cerevisiae | - |
dc.subject.local | saccharomyces cerevisiae | - |
dc.subject.local | Squalene | - |
dc.description.journalClass | Y | - |
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