Engineering the oleaginous yeast Yarrowia lipolytica for β-farnesene overproduction

被引:41
作者
Shi, Tianqiong [1 ]
Li, Yawen [1 ]
Zhu, Li [2 ]
Tong, Yangyang [3 ]
Yang, Junjie [3 ]
Fang, Yunming [4 ]
Wang, Meng [4 ]
Zhang, Jieze [5 ]
Jiang, Yu [6 ,7 ]
Yang, Sheng [3 ,7 ]
机构
[1] Nanjing Normal Univ, Sch Food Sci & Pharmaceut Engn, Nanjing, Peoples R China
[2] Shanghai Laiyi Ctr Biopharmaceut R&D, Shanghai, Peoples R China
[3] Chinese Acad Sci, CAS Ctr Excellence Mol Plant Sci, Key Lab Synthet Biol, 300 Fenglin Rd, Shanghai 200032, Peoples R China
[4] Beijing Univ Chem Technol, Coll Chem Engn, Beijing, Peoples R China
[5] Univ Southern Calif, Dept Chem, Los Angeles, CA 90007 USA
[6] Shanghai Taoyusheng Biotechnol Co Ltd, Shanghai, Peoples R China
[7] Chinese Acad Sci, Shanghai Inst Biol Sci, Huzhou Ctr Ind Biotechnol, Huzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
DAG acyltransferase; fatty acid biosynthesis; metabolic engineering; Yarrowia lipolytica; β ‐ farnesene; BIOSYNTHESIS; EXPRESSION; PATHWAY; METABOLISM; LYCOPENE; SYNTHASE; PRODUCT;
D O I
10.1002/biot.202100097
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
beta-farnesene is a sesquiterpenoid with various industrial applications which is now commercially produced by a Saccharomyces cerevisiae strain obtained by random mutagenesis and genetic engineering. We rationally designed a genetically defined Yarrowia lipolytica through recovery of L-leucine biosynthetic route, gene dosage optimization of beta-farnesene synthase and disruption of the competition pathway. The resulting beta-farnesene titer was improved from 8 to 345 mg L-1. Finally, the strategy for decreasing the lipid accumulation by individually and iteratively knocking out four acyltransferases encoding genes was adopted. The result displayed that beta-farnesene titer in the engineered strain CIBT6304 in which acyltransferases (DGA1 and DGA2) were deleted increased by 45% and reached 539 mg L-1 (88 mg g(-1) DCW). Using fed-batch fermentation, CIBT6304 could produce the highest beta-farnesene titer (22.8 g L-1) among the genetically defined strains. This study will provide the foundation of engineering Y. lipolytica to produce other terpenoids more cost-efficiently.
引用
收藏
页数:8
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