Co-expression of two heterologous lactate dehydrogenases genes in Kluyveromyces marxianus for l-lactic acid production = Kluyveromyces marxianus에서 D형 젖산 생산을 위한 2종의 이형 lactate dehydrogenases 동시 발현

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dc.contributor.authorJ W Lee-
dc.contributor.authorJ H In-
dc.contributor.authorJ B Park-
dc.contributor.authorJonghyeok Shin-
dc.contributor.authorJ H Park-
dc.contributor.authorBong Hyun Sung-
dc.contributor.authorJung Hoon Sohn-
dc.contributor.authorJ H Seo-
dc.contributor.authorJ B Park-
dc.contributor.authorS R Kim-
dc.contributor.authorD H Kweon-
dc.date.accessioned2017-04-19T10:30:15Z-
dc.date.available2017-04-19T10:30:15Z-
dc.date.issued2017-
dc.identifier.issn0168-1656-
dc.identifier.uri10.1016/j.jbiotec.2016.11.015ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/13553-
dc.description.abstractLactic acid (LA) is a versatile compound used in the food, pharmaceutical, textile, leather, and chemical industries. Biological production of LA is possible by yeast strains expressing a bacterial gene encoding L-lactate dehydrogenase (LDH). Kluyveromyces marxianus is an emerging non-conventional yeast with various phenotypes of industrial interest. However, it has not been extensively studied for LA production. In this study, K. marxianus was engineered to express and co-express various heterologous LDH enzymes that were reported to have different pH optimums. Specifically, three LDH enzymes originating from Staphylococcus epidermidis (SeLDH; optimal at pH 5.6), Lactobacillus acidophilus (LaLDH; optimal at pH 5.3), and Bos taurus (BtLDH; optimal at pH 9.8) were functionally expressed individually and in combination in K. marxianus, and the resulting strains were compared in terms of LA production. A strain co-expressing SeLDH and LaLDH (KM5 La + SeLDH) produced 16.0 g/L LA, whereas the strains expressing those enzymes individually produced only 8.4 and 6.8 g/L, respectively. This co-expressing strain produced 24.0 g/L LA with a yield of 0.48 g/g glucose in the presence of CaCO3. Our results suggest that co-expression of LDH enzymes with different pH optimums provides sufficient LDH activity under dynamic intracellular pH conditions, leading to enhanced production of LA compared to individual expression of the LDH enzymes.-
dc.publisherElsevier-
dc.titleCo-expression of two heterologous lactate dehydrogenases genes in Kluyveromyces marxianus for l-lactic acid production = Kluyveromyces marxianus에서 D형 젖산 생산을 위한 2종의 이형 lactate dehydrogenases 동시 발현-
dc.title.alternativeCo-expression of two heterologous lactate dehydrogenases genes in Kluyveromyces marxianus for l-lactic acid production-
dc.typeArticle-
dc.citation.titleJournal of Biotechnology-
dc.citation.number0-
dc.citation.endPage86-
dc.citation.startPage81-
dc.citation.volume241-
dc.contributor.affiliatedAuthorJonghyeok Shin-
dc.contributor.affiliatedAuthorBong Hyun Sung-
dc.contributor.affiliatedAuthorJung Hoon Sohn-
dc.contributor.alternativeName이재원-
dc.contributor.alternativeName인정훈-
dc.contributor.alternativeName박준범-
dc.contributor.alternativeName신종혁-
dc.contributor.alternativeName박진환-
dc.contributor.alternativeName성봉현-
dc.contributor.alternativeName손정훈-
dc.contributor.alternativeName서진호-
dc.contributor.alternativeName박진병-
dc.contributor.alternativeName김수린-
dc.contributor.alternativeName권대혁-
dc.identifier.bibliographicCitationJournal of Biotechnology, vol. 241, pp. 81-86-
dc.identifier.doi10.1016/j.jbiotec.2016.11.015-
dc.subject.keywordCo-expression-
dc.subject.keywordKluyveromyces marxianus-
dc.subject.keywordLactate dehydrogenase-
dc.subject.keywordLactic acid-
dc.subject.keywordOptimal pH-
dc.subject.localCo-expression-
dc.subject.localCoexpression-
dc.subject.localcoexpression-
dc.subject.localKluyveromyces marxianus-
dc.subject.localLactate dehydrogenase-
dc.subject.localLactic acid-
dc.subject.locallactic acid-
dc.subject.locallactic acid (LA)-
dc.subject.localOptimal pH-
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
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