Biosynthesis of adipic acid in metabolically engineered Saccharomyces cerevisiae

被引:12
|
作者
Zhang, Xi [1 ,3 ]
Liu, Yingli [2 ]
Wang, Jing [2 ]
Zhao, Yunying [1 ,4 ]
Deng, Yu [1 ,3 ,4 ]
机构
[1] Jiangnan Univ, Sch Biotechnol, Natl Engn Lab Cereal Fermentat Technol NELCF, 1800 Lihu Rd, Wuxi 214122, Jiangsu, Peoples R China
[2] Beijing Technol & Business Univ, China Canada Joint Lab Food Nutr & Hlth Beijing, Beijing 100048, Peoples R China
[3] Jiangnan Univ, Sch Biotechnol, 1800 Lihu Rd, Wuxi 214122, Jiangsu, Peoples R China
[4] Jiangnan Univ, Jiangsu Prov Res Ctr Bioact Prod Proc Technol, 1800 Lihu Rd, Wuxi 214122, Jiangsu, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Saccharomyces cerevisiae; adipic acid; reverse adipate degradation pathway (RADP); metabolic engineering; fermentation; ESCHERICHIA-COLI; GENE-EXPRESSION; THERMOBIFIDA-FUSCA; GLYCOLYTIC FLUX; YEAST; PATHWAY; INTEGRATION; STRATEGIES; MOLECULES; DEMAND;
D O I
10.1007/s12275-020-0261-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Adipic Acid (AA) is a valued platform chemical compound, which can be used as a precursor of nylon-6,6. Due to the generation of an enormous amount of nitric oxide metabolites and the growing depletion of oil resources as a result of AA production from a mixture of cyclohexanol and cyclohexanone, the microbial methods for synthesizing AA have attracted significant attention. Of the several AA-producing pathways, the reverse adipate degradation pathway in Thermobifida fusca (Tfu RADP) is reported to be the most efficient, which has been confirmed in Escherichia coli. In this study, the heterologous Tfu RADP was constructed for producing AA in S. cerevisiae by co-expressing genes of Tfu_0875, Tfu_2399, Tfu_0067, Tfu_1647, Tfu_2576, and Tfu_2576. The AA titer combined with biomass, cofactors and other by-products was all determined after fermentation. During batch fermentation in a shake flask, the maximum AA titer was 3.83 mg/L, while the titer increased to 10.09 mg/L during fed-batch fermentation in a 5-L bioreactor after fermentation modification.
引用
收藏
页码:1065 / 1075
页数:11
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