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Regulating the metabolic flux of pyruvate dehydrogenase bypass to enhance lipid production in Saccharomyces cerevisiae.
- Source :
-
Communications biology [Commun Biol] 2024 Oct 26; Vol. 7 (1), pp. 1399. Date of Electronic Publication: 2024 Oct 26. - Publication Year :
- 2024
-
Abstract
- To achieve high efficiency in microbial cell factories, it is crucial to redesign central carbon fluxes to ensure an adequate supply of precursors for producing high-value compounds. In this study, we employed a multi-omics approach to rearrange the central carbon flux of the pyruvate dehydrogenase (PDH) bypass, thereby enhancing the supply of intermediate precursors, specifically acetyl-CoA. This enhancement aimed to improve the biosynthesis of acetyl-CoA-derived compounds, such as terpenoids and fatty acid-derived molecules, in Saccharomyces cerevisiae. Through transcriptomic and lipidomic analyses, we identified ALD4 as a key regulatory gene influencing lipid metabolism. Genetic validation demonstrated that overexpression of the mitochondrial acetaldehyde dehydrogenase (ALDH) gene ALD4 resulted in a 20.1% increase in lipid production. This study provides theoretical support for optimising the performance of S. cerevisiae as a "cell factory" for the production of commercial compounds.<br /> (© 2024. The Author(s).)
- Subjects :
- Saccharomyces cerevisiae Proteins metabolism
Saccharomyces cerevisiae Proteins genetics
Lipids biosynthesis
Acetyl Coenzyme A metabolism
Gene Expression Regulation, Fungal
Metabolic Engineering methods
Aldehyde Oxidoreductases metabolism
Aldehyde Oxidoreductases genetics
Saccharomyces cerevisiae genetics
Saccharomyces cerevisiae metabolism
Pyruvate Dehydrogenase Complex metabolism
Pyruvate Dehydrogenase Complex genetics
Lipid Metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2399-3642
- Volume :
- 7
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Communications biology
- Publication Type :
- Academic Journal
- Accession number :
- 39462103
- Full Text :
- https://doi.org/10.1038/s42003-024-07103-7