In silico identification of metabolic engineering strategies for improved lipid production in Yarrowia lipolytica by genome-scale metabolic modeling

被引:35
作者
Kim, Minsuk [1 ,5 ]
Park, Beom Gi [2 ,3 ]
Kim, Eun-Jung [3 ,4 ]
Kim, Joonwon [2 ,3 ]
Kim, Byung-Gee [2 ,3 ,4 ]
机构
[1] Seoul Natl Univ, Inst Engn Res, Seoul 08826, South Korea
[2] Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 08826, South Korea
[3] Seoul Natl Univ, Inst Mol Biol & Genet, Seoul 08826, South Korea
[4] Seoul Natl Univ, BioMAX Inst, Seoul 08826, South Korea
[5] Mayo Clin, Ctr Individualized Med, Microbiome Program, Rochester, MN 55905 USA
基金
新加坡国家研究基金会;
关键词
Genome-scale modeling; Systems biology; Metabolic engineering; Yarrowia lipolytica; eMOMA; Lipid; Non-conventional yeast; TAG; CONSTRAINT-BASED MODELS; OLEAGINOUS MICROORGANISMS; MALIC ENZYME; ACCUMULATION; OPTIMIZATION; RECONSTRUCTION; OVERPRODUCTION; STRAINS; PATHWAY; NADPH;
D O I
10.1186/s13068-019-1518-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
BackgroundYarrowia lipolytica, an oleaginous yeast, is a promising platform strain for production of biofuels and oleochemicals as it can accumulate a high level of lipids in response to nitrogen limitation. Accordingly, many metabolic engineering efforts have been made to develop engineered strains of Y. lipolytica with higher lipid yields. Genome-scale model of metabolism (GEM) is a powerful tool for identifying novel genetic designs for metabolic engineering. Several GEMs for Y. lipolytica have recently been developed; however, not many applications of the GEMs have been reported for actual metabolic engineering of Y. lipolytica. The major obstacle impeding the application of Y. lipolytica GEMs is the lack of proper methods for predicting phenotypes of the cells in the nitrogen-limited condition, or more specifically in the stationary phase of a batch culture.ResultsIn this study, we showed that environmental version of minimization of metabolic adjustment (eMOMA) can be used for predicting metabolic flux distribution of Y. lipolytica under the nitrogen-limited condition and identifying metabolic engineering strategies to improve lipid production in Y. lipolytica. Several well-characterized overexpression targets, such as diglyceride acyltransferase, acetyl-CoA carboxylase, and stearoyl-CoA desaturase, were successfully rediscovered by our eMOMA-based design method, showing the relevance of prediction results. Interestingly, the eMOMA-based design method also suggested non-intuitive knockout targets, and we experimentally validated the prediction with a mutant lacking YALI0F30745g, one of the predicted targets involved in one-carbon/methionine metabolism. The mutant accumulated 45% more lipids compared to the wild-type.ConclusionThis study demonstrated that eMOMA is a powerful computational method for understanding and engineering the metabolism of Y. lipolytica and potentially other oleaginous microorganisms.
引用
收藏
页码:1 / 14
页数:14
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