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Engineering yeast phospholipid metabolism for de novo oleoylethanolamide production

Nat Chem Biol. 2020; 
Liu Y, Liu Q, Krivoruchko A, , Khoomrung S, Nielsen J, ,
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Gene Synthesis All plasmids and strains used in this study are listed in Supplementary Tables 2 and 3, respectively. High-fdelity Phusion DNA polymerase and Gibson assembly kit were purchased from NEB. PrimeStar DNA polymerase and SapphireAmp Fast PCR Master Mix were purchased from TaKaRa Bio. Restriction enzymes and plasmid miniprep and DNA gel purifcation kits were purchased from Termo Scientifc. S. cerevisiae codon-optimized genes were synthesized by GenScript and are listed in Supplementary Table 4. Get A Quote

摘要

Phospholipids, the most abundant membrane lipid components, are crucial in maintaining membrane structures and homeostasis for biofunctions. As a structurally diverse and tightly regulated system involved in multiple organelles, phospholipid metabolism is complicated to manipulate. Thus, repurposing phospholipids for lipid-derived chemical production remains unexplored. Herein, we develop a Saccharomyces cerevisiae platform for de novo production of oleoylethanolamide, a phospholipid derivative with promising pharmacological applications in ameliorating lipid dysfunction and neurobehavioral symptoms. Through deregulation of phospholipid metabolism, screening of biosynthetic enzymes, engineering of subcellular t... More

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