4.7 Article

Increasing lipid yield in Yarrowia lipolytica through phosphoketolase and phosphotransacetylase expression in a phosphofructokinase deletion strain

Journal

BIOTECHNOLOGY FOR BIOFUELS
Volume 14, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13068-021-01962-6

Keywords

Phosphotransacetylase; Phosphoketolase; Lipid yield; Cell-specific lipid productivity; Yarrowia lipolytica; Central carbon metabolism

Funding

  1. Novogy Inc.

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In this study, a heterologous pathway was constructed in Y. lipolytica to redirect carbon flux from glucose to acetyl-CoA, resulting in improved lipid yield and cell-specific productivity. By engineering the Xpk/Pta pathway, the strain showed enhanced performance in large-scale lipid fermentations, paving the way for Y. lipolytica to become a preferred microbial biocatalyst for lipid production in industry.
Background Lipids are important precursors in the biofuel and oleochemical industries. Yarrowia lipolytica is among the most extensively studied oleaginous microorganisms and has been a focus of metabolic engineering to improve lipid production. Yield improvement, through rewiring of the central carbon metabolism of Y. lipolytica from glucose to the lipid precursor acetyl-CoA, is a key strategy for achieving commercial success in this organism. Results Building on YB-392, a Y. lipolytica isolate known for stable non-hyphal growth and low citrate production with demonstrated potential for high lipid accumulation, we assembled a heterologous pathway that redirects carbon flux from glucose through the pentose phosphate pathway (PPP) to acetyl-CoA. We used phosphofructokinase (Pfk) deletion to block glycolysis and expressed two non-native enzymes, phosphoketolase (Xpk) and phosphotransacetylase (Pta), to convert PPP-produced xylulose-5-P to acetyl-CoA. Introduction of the pathway in a pfk deletion strain that is unable to grow and accumulate lipid from glucose in defined media ensured maximal redirection of carbon flux through Xpk/Pta. Expression of Xpk and Pta restored growth and lipid production from glucose. In 1-L bioreactors, the engineered strains recorded improved lipid yield and cell-specific productivity by up to 19 and 78%, respectively. Conclusions Yields and cell-specific productivities are important bioprocess parameters for large-scale lipid fermentations. Improving these parameters by engineering the Xpk/Pta pathway is an important step towards developing Y. lipolytica as an industrially preferred microbial biocatalyst for lipid production.

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