Comparison and Analysis of Published Genome-scale Metabolic Models of Yarrowia lipolytica

被引:9
|
作者
Xu, Yu [1 ]
Holic, Roman [2 ]
Hua, Qiang [1 ,3 ]
机构
[1] East China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
[2] Slovak Acad Sci, Inst Anim Biochem & Genet, Ctr Biosci, Dubravska Cesta 9, Bratislava, Slovakia
[3] Shanghai Collaborat Innovat Ctr Biomfg, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
genome-scale metabolic models; Yarrowia lipolytica; intracellular flux distribution; simulation of cell growth and production; RECONSTRUCTION; OVERPRODUCTION; CULTURE; KEGG;
D O I
10.1007/s12257-019-0208-1
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
Background Genome-scale metabolic models (GEMs) are powerful tools for predicting metabolic flux distributions, understanding complex cell physiology, and guiding the improvement of cell metabolism and production. Yarrowia lipolytica is known for its ability to accumulate lipids and has been widely employed to produce many important metabolites as an ideal host microorganism. There are six GEMs reconstructed for this strain by different research groups, which, however, may cause confusion for model users. It is therefore necessary to understand and analyze the existing models comprehensively. Results Different simulation results of the published GEMs of Y. lipolytica were analyzed based on experimental data, in order to understand the differences among models and identify whether there were common problems in model construction. First, specific growth rates (mu) under various culture conditions were simulated by different models, showing that the biomass generation equation in models had significant influence on the accuracy of simulation results. In addition, simulation and analysis of intracellular flux distributions revealed several inaccurate descriptions on the reversibility of reactions involving currency metabolites in the models. Finally, specific metabolite formation rates were predicted for different target products, and large discrepancies among the different models were observed. The corresponding solutions were then proposed according to the findings of the above model problems. Conclusions We have corrected the existing GEMs of Y. lipolytica and the prediction performances of the models have been significantly improved. Several suggestions for better construction and refinement of genome-scale metabolic network models were also provided.
引用
收藏
页码:53 / 61
页数:9
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