TY - JOUR
T1 - Engineering yeast for the production of breviscapine by genomic analysis and synthetic biology approaches
AU - Liu, Xiaonan
AU - Cheng, Jian
AU - Zhang, Guanghui
AU - Ding, Wentao
AU - Duan, Lijin
AU - Yang, Jing
AU - Kui, Ling
AU - Cheng, Xiaozhi
AU - Ruan, Jiangxing
AU - Fan, Wei
AU - Chen, Junwen
AU - Long, Guangqiang
AU - Zhao, Yan
AU - Cai, Jing
AU - Wang, Wen
AU - Ma, Yanhe
AU - Dong, Yang
AU - Yang, Shengchao
AU - Jiang, Huifeng
N1 - Publisher Copyright:
© 2018 The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85041278858&partnerID=8YFLogxK
U2 - 10.1038/s41467-018-02883-z
DO - 10.1038/s41467-018-02883-z
M3 - 文章
C2 - 29386648
AN - SCOPUS:85041278858
SN - 2041-1723
VL - 9
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 448
ER -