共 36 条
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.
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