Efficient production of levan using a recombinant yeast Saccharomyces cerevisiae hypersecreting a bacterial levansucrase

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dc.contributor.authorHyunjun Ko-
dc.contributor.authorJung Hoon Bae-
dc.contributor.authorBong Hyun Sung-
dc.contributor.authorMi Jin Kim-
dc.contributor.authorChul Ho Kim-
dc.contributor.authorBaek Rock Oh-
dc.contributor.authorJung Hoon Sohn-
dc.date.accessioned2020-02-07T16:30:28Z-
dc.date.available2020-02-07T16:30:28Z-
dc.date.issued2019-
dc.identifier.issn0169-4146-
dc.identifier.uri10.1007/s10295-019-02206-1ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/19124-
dc.description.abstractLevan is a fructose polymer with diverse applications in the food and medical industries. In this study, levansucrase from Rahnella aquatilis (RaLsrA) was hyper-secreted using a Saccharomyces cerevisiae protein secretion system. An optimal secretion signal, a translation fusion partner (TFP) containing an N-terminal 98 amino acid domain from a mitochondrial inner membrane protein, UTH1, was employed to secrete approximately 50 U/mL of bioactive RaLsrA into culture media with 63% secretion efficiency by fed-batch fermentation. Although the purified RaLsrA was useful for enzymatic conversion of high-molecular-weight levan of approximately 3.75×106 Da, recombinant yeast secreting RaLsrA could produce levan more efficiently by microbial fermentation. In a 50-L scale fermenter, 76-g/L levan was directly converted from 191-g/L sucrose by recombinant yeast cells, attaining an 80% conversion yield and 3.17-g/L/h productivity. Thus, we developed a cost-effective and industrially applicable production system for food-grade levan.-
dc.publisherSpringer-
dc.titleEfficient production of levan using a recombinant yeast Saccharomyces cerevisiae hypersecreting a bacterial levansucrase-
dc.title.alternativeEfficient production of levan using a recombinant yeast Saccharomyces cerevisiae hypersecreting a bacterial levansucrase-
dc.typeArticle-
dc.citation.titleJournal of Industrial Microbiology & Biotechnology-
dc.citation.number11-
dc.citation.endPage1620-
dc.citation.startPage1611-
dc.citation.volume46-
dc.contributor.affiliatedAuthorHyunjun Ko-
dc.contributor.affiliatedAuthorJung Hoon Bae-
dc.contributor.affiliatedAuthorBong Hyun Sung-
dc.contributor.affiliatedAuthorMi Jin Kim-
dc.contributor.affiliatedAuthorChul Ho Kim-
dc.contributor.affiliatedAuthorBaek Rock Oh-
dc.contributor.affiliatedAuthorJung Hoon Sohn-
dc.contributor.alternativeName고현준-
dc.contributor.alternativeName배정훈-
dc.contributor.alternativeName성봉현-
dc.contributor.alternativeName김미진-
dc.contributor.alternativeName김철호-
dc.contributor.alternativeName오백록-
dc.contributor.alternativeName손정훈-
dc.identifier.bibliographicCitationJournal of Industrial Microbiology & Biotechnology, vol. 46, no. 11, pp. 1611-1620-
dc.identifier.doi10.1007/s10295-019-02206-1-
dc.subject.keywordDirect fermentation-
dc.subject.keywordLevan-
dc.subject.keywordLevansucrase-
dc.subject.keywordRecombinant protein expression-
dc.subject.keywordSaccharomyces cerevisiae-
dc.subject.localDirect fermentation-
dc.subject.localLevan-
dc.subject.locallevan-
dc.subject.localLevansucrase-
dc.subject.locallevansucrase-
dc.subject.localRecombinant protein expression-
dc.subject.localrecombinant protein expression-
dc.subject.localSaccharomyces cerevisiae-
dc.subject.localsaccharomyces cerevisiae-
dc.description.journalClassY-
Appears in Collections:
Synthetic Biology and Bioengineering Research Institute > Synthetic Biology Research Center > 1. Journal Articles
Synthetic Biology and Bioengineering Research Institute > 1. Journal Articles
Jeonbuk Branch Institute > Microbial Biotechnology Research Center > 1. Journal Articles
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