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In silico identification of metabolic engineering strategies for improved lipid production in Yarrowia lipolytica by genome-scale metabolic modeling
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, Minsuk | - |
dc.contributor.author | Park, Beom Gi | - |
dc.contributor.author | Kim, Eun-Jung | - |
dc.contributor.author | Kim, Joonwon | - |
dc.contributor.author | Kim, Byung-Gee | - |
dc.date.accessioned | 2019-10-30T00:27:30Z | - |
dc.date.available | 2019-10-30T09:38:24Z | - |
dc.date.issued | 2019-07-24 | - |
dc.identifier.citation | Biotechnology for Biofuels, 12(1):187 | ko_KR |
dc.identifier.issn | 1754-6834 | - |
dc.identifier.uri | https://hdl.handle.net/10371/162579 | - |
dc.description.abstract | Background
Yarrowia 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. Results In 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. Conclusion This study demonstrated that eMOMA is a powerful computational method for understanding and engineering the metabolism of Y. lipolytica and potentially other oleaginous microorganisms. | ko_KR |
dc.description.sponsorship | This research was supported by the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (NRF2017R1E1A1A01073523) and Industrial Strategic technology development program, 20002734 funded by the Ministry of Trade, Industry & Energy (MI,
Korea) | ko_KR |
dc.language.iso | en | ko_KR |
dc.publisher | BioMed Central | ko_KR |
dc.subject | Genome-scale modeling | ko_KR |
dc.subject | Systems biology | ko_KR |
dc.subject | Metabolic engineering | ko_KR |
dc.subject | Yarrowia lipolytica | ko_KR |
dc.subject | eMOMA | ko_KR |
dc.subject | Lipid | ko_KR |
dc.subject | Non-conventional yeast | ko_KR |
dc.subject | TAG | ko_KR |
dc.title | In silico identification of metabolic engineering strategies for improved lipid production in Yarrowia lipolytica by genome-scale metabolic modeling | ko_KR |
dc.type | Article | ko_KR |
dc.contributor.AlternativeAuthor | 김민석 | - |
dc.contributor.AlternativeAuthor | 박범기 | - |
dc.contributor.AlternativeAuthor | 김은정 | - |
dc.contributor.AlternativeAuthor | 김준원 | - |
dc.contributor.AlternativeAuthor | 김병기 | - |
dc.identifier.doi | 10.1186/s13068-019-1518-4 | - |
dc.language.rfc3066 | en | - |
dc.rights.holder | The Author(s) | - |
dc.date.updated | 2019-07-28T03:40:51Z | - |
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