Harnessing Yarrowia lipolytica lipogenesis to create a platform for lipid and biofuel production

被引:451
|
作者
Blazeck, John [1 ]
Hill, Andrew [1 ]
Liu, Leqian [1 ]
Knight, Rebecca [2 ]
Miller, Jarrett [1 ]
Pan, Anny [1 ]
Otoupal, Peter [1 ]
Alper, Hal S. [1 ,3 ]
机构
[1] Univ Texas Austin, McKetta Dept Chem Engn, Austin, TX 78712 USA
[2] Univ Texas Austin, Sect Mol Cell & Dev Biol, Austin, TX 78712 USA
[3] Univ Texas Austin, Inst Cellular & Mol Biol, Austin, TX 78712 USA
来源
NATURE COMMUNICATIONS | 2014年 / 5卷
关键词
TRANSFER-RNA SYNTHETASE; FREE FATTY-ACIDS; OLEAGINOUS YEAST; HETEROLOGOUS PROTEINS; GENE-EXPRESSION; MALIC ENZYME; ACCUMULATION; VECTORS; FUELS; IDENTIFICATION;
D O I
10.1038/ncomms4131
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Economic feasibility of biosynthetic fuel and chemical production hinges upon harnessing metabolism to achieve high titre and yield. Here we report a thorough genotypic and phenotypic optimization of an oleaginous organism to create a strain with significant lipogenesis capability. Specifically, we rewire Yarrowia lipolytica's native metabolism for superior de novo lipogenesis by coupling combinatorial multiplexing of lipogenesis targets with phenotypic induction. We further complete direct conversion of lipid content into biodiesel. Tri-level metabolic control results in saturated cells containing upwards of 90% lipid content and titres exceeding 25 g l(-1) lipids, which represents a 60-fold improvement over parental strain and conditions. Through this rewiring effort, we advance fundamental understanding of lipogenesis, demonstrate non-canonical environmental and intracellular stimuli and uncouple lipogenesis from nitrogen starvation. The high titres and carbon-source independent nature of this lipogenesis in Y. lipolytica highlight the potential of this organism as a platform for efficient oleochemical production.
引用
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页数:10
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