Abstract
Fatty acids produced by the yeast, Saccharomyces cerevisiae, are not only industrially important products, but also highly affect fermentation efficiency. Despite that S. cerevisiae is the potent metabolic platform, traditional plasmid-based genetic manipulations still impose concerns about safety and environmental impact. In this study, using the Cas9 system, S. cerevisiae, was metabolically engineered for increased production of fatty acids by increasing cytosolic acetyl-CoA production via disrupting the isocitrate dehydrogenase gene of the TCA cycle and introducing the cytosolic ATP-citrate lyase gene from Yarrowia lipolytica. By expressing the ATP-citrate lyase gene from Y. lipolytica, total fatty acid production increased by 37.1% compared to that by the wild-type yeast. This total fatty acid production herein increased ∼2 times compared to that by an engineered S. cerevisiae in a previous report, and unsaturated fatty acid levels also increased. Our results suggest that the Cas9 system for S. cerevisiae could be applied to engineer the yeast for industrial production of bio-based products.
Original language | English |
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Pages (from-to) | 23-28 |
Number of pages | 6 |
Journal | Process Biochemistry |
Volume | 73 |
DOIs | |
Publication status | Published - 2018 Oct |
Keywords
- ATP-citrate lyase
- CRISPR
- Cas9
- Fatty acids
- Isocitrate dehydrogenase
- Saccharomyces cerevisiae
ASJC Scopus subject areas
- Bioengineering
- Biochemistry
- Applied Microbiology and Biotechnology