De Novo Biosynthesis of Polydatin in Saccharomyces cerevisiae

被引:8
|
作者
Liu, Tian [1 ,2 ,3 ]
Liu, Yuqian [2 ,3 ,4 ]
Li, Lan [5 ,6 ]
Liu, Xiaonan [2 ,3 ]
Guo, Zhaokuan [2 ,3 ]
Cheng, Jian [2 ,3 ]
Zhu, Xiaoxi [2 ]
Lu, Lina [2 ,3 ]
Zhang, Junlin [7 ]
Fan, Guanwei [5 ,6 ]
Xie, Nengzhong [8 ]
Lu, Jian [1 ]
Jiang, Huifeng [2 ,3 ]
机构
[1] Guangxi Univ, Life Sci & Technol Coll, Nanning 530004, Guangxi, Peoples R China
[2] Chinese Acad Sci, Tianjin Inst Ind Biotechnol, Key Lab Syst Microbial Biotechnol, Tianjin 300308, Peoples R China
[3] Natl Ctr Technol Innovat Synthet Biol, Tianjin 300308, Peoples R China
[4] South China Univ Technol, Sch Biol & Biol Engn, Guangzhou 510006, Guangdong, Peoples R China
[5] Tianjin Univ Tradit Chinese Med, Teaching Hosp 1, Tianjin 300193, Peoples R China
[6] Tianjin Univ Tradit Chinese Med, Tianjin Key Lab Translat Res TCM Prescript & Synd, Tianjin 301617, Peoples R China
[7] Wuhan Polytech Univ, Coll Life Sci & Technol, Wuhan 430023, Hubei, Peoples R China
[8] Guangxi Acad Sci, Natl Engn Res Ctr Nonfood Biorefinery, Guangxi Biomass Engn Technol Res Ctr, State Key Lab Nonfood Biomass & Enzyme Technol, Nanning 530007, Guangxi, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Polygonum cuspidatum; polydatin; resveratrol; glycosyltransferase; synthetic biology; RESVERATROL; GLYCOSYLTRANSFERASE; GLYCOSYLATION; PHARMACOLOGY; MOLECULES; GLUCOSE; ACID;
D O I
10.1021/acs.jafc.1c01557
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Polydatin, with better structural stability and biological activities than resveratrol, is mainly extracted from the traditional Chinese medicinal plant Polygonum cuspidatum. In this study, based on the transcriptome analysis of P. cuspidatum, we identified the key glycosyltransferase of resveratrol and achieved the biosynthesis of polydatin from glucose by incorporation with the resveratrol biosynthesis module, UDP-glucose supply module, and glycosyltransferase expression module. Through metabolic engineering and fermentation optimization, the production of polydatin reached 545 mg/L, and the dry cell weight was 27.83 mg/g DCW, which was about twice that of extracted from the P. cuspidatum root (11.404 mg/g DCW). Therefore, it is possible to replace the production mode of polydatin from plant extraction to microbial chassis in the future.
引用
收藏
页码:5917 / 5925
页数:9
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