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Knocking out central metabolism genes to identify new targets and alternating substrates to improve lipid synthesis in Y. lipolytica
Introduction: Systematic gene knockout studies may offer us novel insights on cell metabolism and physiology. Specifically, the lipid accumulation mechanism at the molecular or cellular level is yet to be determined in the oleaginous yeast Y. lipolytica. Methods: Herein, we established ten engineere...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880266/ https://www.ncbi.nlm.nih.gov/pubmed/36714010 http://dx.doi.org/10.3389/fbioe.2023.1098116 |
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author | Zhu, Jiang Gu, Yang Yan, Yijing Ma, Jingbo Sun, Xiaoman Xu, Peng |
author_facet | Zhu, Jiang Gu, Yang Yan, Yijing Ma, Jingbo Sun, Xiaoman Xu, Peng |
author_sort | Zhu, Jiang |
collection | PubMed |
description | Introduction: Systematic gene knockout studies may offer us novel insights on cell metabolism and physiology. Specifically, the lipid accumulation mechanism at the molecular or cellular level is yet to be determined in the oleaginous yeast Y. lipolytica. Methods: Herein, we established ten engineered strains with the knockout of important genes involving in central carbon metabolism, NADPH generation, and fatty acid biosynthetic pathways. Results: Our result showed that NADPH sources for lipogenesis include the OxPP pathway, POM cycle, and a trans-mitochondrial isocitrate-α-oxoglutarate NADPH shuttle in Y. lipolytica. Moreover, we found that knockout of mitochondrial NAD(+) isocitrate dehydrogenase IDH2 and overexpression of cytosolic NADP(+) isocitrate dehydrogenase IDP2 could facilitate lipid synthesis. Besides, we also demonstrated that acetate is a more favorable carbon source for lipid synthesis when glycolysis step is impaired, indicating the evolutionary robustness of Y. lipolytica. Discussion: This systematic investigation of gene deletions and overexpression across various lipogenic pathways would help us better understand lipogenesis and engineer yeast factories to upgrade the lipid biomanufacturing platform. |
format | Online Article Text |
id | pubmed-9880266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98802662023-01-28 Knocking out central metabolism genes to identify new targets and alternating substrates to improve lipid synthesis in Y. lipolytica Zhu, Jiang Gu, Yang Yan, Yijing Ma, Jingbo Sun, Xiaoman Xu, Peng Front Bioeng Biotechnol Bioengineering and Biotechnology Introduction: Systematic gene knockout studies may offer us novel insights on cell metabolism and physiology. Specifically, the lipid accumulation mechanism at the molecular or cellular level is yet to be determined in the oleaginous yeast Y. lipolytica. Methods: Herein, we established ten engineered strains with the knockout of important genes involving in central carbon metabolism, NADPH generation, and fatty acid biosynthetic pathways. Results: Our result showed that NADPH sources for lipogenesis include the OxPP pathway, POM cycle, and a trans-mitochondrial isocitrate-α-oxoglutarate NADPH shuttle in Y. lipolytica. Moreover, we found that knockout of mitochondrial NAD(+) isocitrate dehydrogenase IDH2 and overexpression of cytosolic NADP(+) isocitrate dehydrogenase IDP2 could facilitate lipid synthesis. Besides, we also demonstrated that acetate is a more favorable carbon source for lipid synthesis when glycolysis step is impaired, indicating the evolutionary robustness of Y. lipolytica. Discussion: This systematic investigation of gene deletions and overexpression across various lipogenic pathways would help us better understand lipogenesis and engineer yeast factories to upgrade the lipid biomanufacturing platform. Frontiers Media S.A. 2023-01-13 /pmc/articles/PMC9880266/ /pubmed/36714010 http://dx.doi.org/10.3389/fbioe.2023.1098116 Text en Copyright © 2023 Zhu, Gu, Yan, Ma, Sun and Xu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Zhu, Jiang Gu, Yang Yan, Yijing Ma, Jingbo Sun, Xiaoman Xu, Peng Knocking out central metabolism genes to identify new targets and alternating substrates to improve lipid synthesis in Y. lipolytica |
title | Knocking out central metabolism genes to identify new targets and alternating substrates to improve lipid synthesis in Y. lipolytica
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title_full | Knocking out central metabolism genes to identify new targets and alternating substrates to improve lipid synthesis in Y. lipolytica
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title_fullStr | Knocking out central metabolism genes to identify new targets and alternating substrates to improve lipid synthesis in Y. lipolytica
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title_full_unstemmed | Knocking out central metabolism genes to identify new targets and alternating substrates to improve lipid synthesis in Y. lipolytica
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title_short | Knocking out central metabolism genes to identify new targets and alternating substrates to improve lipid synthesis in Y. lipolytica
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title_sort | knocking out central metabolism genes to identify new targets and alternating substrates to improve lipid synthesis in y. lipolytica |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880266/ https://www.ncbi.nlm.nih.gov/pubmed/36714010 http://dx.doi.org/10.3389/fbioe.2023.1098116 |
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