Discovery of a Potential Liver Fibrosis Inhibitor from a Mushroom Endophytic Fungus by Genome Mining of a Silent Biosynthetic Gene Cluster

被引:4
|
作者
Cheng, Jin-Tao [1 ,2 ,3 ]
Wang, Han-Min [4 ,5 ]
Yu, Jia-Hui [6 ]
Sun, Chen-Fan [1 ,2 ,3 ]
Cao, Fei [1 ,2 ,3 ]
Jiang, Xin-Hang [7 ]
Chen, Xin-Ai [1 ,2 ,3 ]
Zhao, Qing-Wei [1 ,2 ]
Gan, Li-She [6 ,8 ]
Xie, Rong-Rong [4 ]
Wang, Shi-Lei [9 ]
Li, Jia [4 ,5 ]
Zang, Yi [4 ,5 ]
Mao, Xu-Ming [1 ,2 ,3 ,10 ]
机构
[1] Zhejiang Univ, Inst Pharmaceut Biotechnol, Affiliated Hosp 1, Sch Med, Hangzhou 310058, Zhejiang, Peoples R China
[2] Zhejiang Univ, Res Ctr Clin Pharm, Affiliated Hosp 1, Sch Med, Hangzhou 310058, Zhejiang, Peoples R China
[3] Zhejiang Prov Key Lab Microbial Biochem & Metab E, Hangzhou 310058, Peoples R China
[4] Chinese Acad Sci, Natl Ctr Drug Screening, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
[5] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[6] Zhejiang Univ, Coll Pharmaceut Sci, Hangzhou 310058, Peoples R China
[7] Zhejiang Univ, Coll Life Sci, Equipment & Technol Serv Platform, Hangzhou 310058, Peoples R China
[8] Wuyi Univ, Sch Biotechnol & Hlth Sci, Jiangmen 529020, Guangdong, Peoples R China
[9] Zhejiang Shuren Univ, Hangzhou 310058, Peoples R China
[10] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, State Key Lab Bioact Subst & Funct Nat Med, Beijing 100050, 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
fungus; Calcarisporium arbuscula; natural product; gene cluster activation; liver fibrosis; DRIVEN DISCOVERY; POLYKETIDE; METABOLITES; ACTIVATION; LEADS; ACID;
D O I
10.1021/acs.jafc.1c03639
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Liver fibrosis has accounted for liver diseases and overall mortality, but no relevant drug has been developed. Filamentous fungi are important resources of natural products for pharmaceutical development. Calcarisporium arbuscula is a mushroom endophytic fungus, which primarily produces aurovertins. Here, in an aurovertin null-production mutant, one silent gene cluster (mcal7) was activated by overexpression of a pathway-specific zinc finger transcriptional regulator, and a tetramic acid-type compound (1, MCA17-1) was identified. Along with detailed structural characterization, its biosynthesis was proposed to be produced from the core PKS-NRPS hybrid enzyme. Moreover, 1 suppressed the activation of LX-2 upon transforming growth factor-beta (TGF-beta) challenge and had stronger bioactivity than the positive control obeticholic acid (OCA) against liver fibrosis. Our work suggested that this engineered fungus could be a producer of 1 for promising pharmaceutical development, and alternatively, it would be developed as a mushroom ingredient in dietary therapy to prevent liver fibrosis.
引用
收藏
页码:11303 / 11310
页数:8
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