RT Journal Article SR Electronic T1 Combinatorial metabolic engineering of Saccharomyces cerevisiae for terminal alkene production JF bioRxiv FD Cold Spring Harbor Laboratory SP 022350 DO 10.1101/022350 A1 Binbin Chen A1 Dong-Yup Lee A1 Matthew Wook Chang YR 2015 UL http://biorxiv.org/content/early/2015/07/20/022350.abstract AB Biological production of terminal alkenes has garnered a significant interest due to their industrial applications such as lubricants, detergents and fuels. Here, we engineered the yeast Saccharomyces cerevisiae to produce terminal alkenes via a one-step fatty acid decarboxylation pathway and improved the alkene production using combinatorial engineering strategies. In brief, we first characterized eight fatty acid decarboxylases to enable and enhance alkene production. We then increased the production titer 7-fold by improving the availability of the precursor fatty acids. We additionally increased the titer about 5-fold through genetic cofactor engineering and gene expression tuning in rich medium. Lastly, we further improved the titer 1.8-fold to 3.7 mg/L by optimizing the culturing conditions in bioreactors. This study represents the first report of terminal alkene biosynthesis in S. cerevisiae, and the abovementioned combinatorial engineering approaches collectively increased the titer 67.4-fold. We envision that these approaches could provide insights into devising engineering strategies to improve the production of fatty acid-derived biochemicals in S. cerevisiae.