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In relation to this article, we declare that there is no conflict of interest.
Publication history
Received September 21, 2018
Accepted January 17, 2019
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Engineering Trichosporon oleaginosus for enhanced production of lipid from volatile fatty acids as carbon source

1Department of Chemical and Biomolecular Engineering (BK21 Program), KAIST, 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Korea 2Cell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, Korea 3Lab to Market, Inc., Nurikkum Square R&D Center, 1013-2 396 World Cup buk-ro, Mapo-gu, Seoul 03925, Korea 4Institute for the BioCentury, KAIST, 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Korea
kjjeong@kaist.ac.kr
Korean Journal of Chemical Engineering, June 2019, 36(6), 903-908(6), 10.1007/s11814-018-0229-7

Abstract

Trichosporon oleaginosus is one of the most promising hosts for microbial lipid production owing to its high-productivity. In an effort to develop an economical production process, we engineered T. oleaginosus towards high-lipid production from volatile fatty acids (VFA) derived from anaerobic fermentation of food waste. First, we established a method for labeling intracellular lipid with lipophilic BODIPY fluorescent dye. Next, a random library was constructed by treatment with a chemical mutagen, and high-lipid producers were screened using fluorescenceactivated cell sorting. Subsequently, one clone, N14, was successfully isolated, which exhibited 3-fold higher lipid production (19.4%) in VFA (6 g/L) media than the wild-type strain, and also showed increased lipid production in higher concentrations of VFA (18 or 24 g/L). Based on fatty acid methyl ester (FAME) analysis, N14 contained higher stearic acid (C18:0) and oleic acid (C18:1) content compared with those of the wild-type strain.

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