Engineering yeast for the production of breviscapine by genomic analysis and synthetic biology approaches

被引:200
作者
Liu, Xiaonan [1 ,2 ]
Cheng, Jian [1 ]
Zhang, Guanghui [3 ]
Ding, Wentao [1 ]
Duan, Lijin [1 ]
Yang, Jing [3 ,4 ]
Kui, Ling [2 ,5 ]
Cheng, Xiaozhi [1 ]
Ruan, Jiangxing [1 ]
Fan, Wei [3 ]
Chen, Junwen [3 ]
Long, Guangqiang [3 ]
Zhao, Yan [3 ]
Cai, Jing [6 ]
Wang, Wen [5 ,7 ]
Ma, Yanhe [1 ]
Dong, Yang [3 ,4 ]
Yang, Shengchao [3 ,4 ]
Jiang, Huifeng [1 ]
机构
[1] Chinese Acad Sci, Tianjin Inst Ind Biotechnol, Key Lab Syst Microbial Biotechnol, Tianjin 300308, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Yunnan Agr Univ, State Key Lab Conservat & Utilizat Bioresources Y, Key Lab Med Plant Biol Yunnan Prov, Kunming 650201, Yunnan, Peoples R China
[4] Natl & Local Joint Engn Res Ctr Germplasm Utiliza, Kunming 650201, Yunnan, Peoples R China
[5] Chinese Acad Sci, Kunming Inst Zool, State Key Lab Genet Resources & Evolut, Kunming 650223, Yunnan, Peoples R China
[6] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Taipa, Macau, Peoples R China
[7] Northwestern Polytech Univ, Ctr Ecol & Environm Sci, Xian 710072, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
UDP-GLUCOSE; WEB SERVER; CLONING; BIOSYNTHESIS; GENE; IDENTIFICATION; EXPRESSION; PRECURSOR; PATHWAY; ACID;
D O I
10.1038/s41467-018-02883-z
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
The flavonoid extract from Erigeron breviscapus, breviscapine, has increasingly been used to treat cardio- and cerebrovascular diseases in China for more than 30 years, and plant supply of E. breviscapus is becoming insufficient to satisfy the growing market demand. Here we report an alternative strategy for the supply of breviscapine by building a yeast cell factory using synthetic biology. We identify two key enzymes in the biosynthetic pathway (flavonoid-7-O-glucuronosyltransferase and flavone-6-hydroxylase) from E. breviscapus genome and engineer yeast to produce breviscapine from glucose. After metabolic engineering and optimization of fed-batch fermentation, scutellarin and apigenin-7-O-glucuronide, two major active ingredients of breviscapine, reach to 108 and 185 mg l(-1), respectively. Our study not only introduces an alternative source of these valuable compounds, but also provides an example of integrating genomics and synthetic biology knowledge for metabolic engineering of natural compounds.
引用
收藏
页数:10
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