Activation of an unconventional meroterpenoid gene cluster in Neosartorya glabra leads to the production of new berkeleyacetals

被引:25
作者
Zhang, Tao [1 ,2 ]
Wan, Jun [1 ,2 ]
Zhan, Zhajun [3 ]
Bai, Jian [1 ,2 ]
Liu, Bingyu [1 ,2 ]
Hu, Youcai [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Inst Mat Med, State Key Lab Bioact Subst & Funct Nat Med, Beijing 100050, Peoples R China
[2] Peking Union Med Coll, Beijing 100050, Peoples R China
[3] Zhejiang Univ Technol, Coll Pharmaceut Sci, Hangzhou 310014, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Neosartorya glabra; Meroterpenoid; Berke teyacetals; Genome mining; Cryptic gene cluster; Biosynthesis; BIOSYNTHETIC-PATHWAY; MULTIFUNCTIONAL CYTOCHROME-P450; DISCOVERY; RING; POLYKETIDES; METABOLITES; DERIVATIVES; AUSTINOL; ENCODES;
D O I
10.1016/j.apsb.2017.12.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Fungal genomes carry many gene clusters seemingly capable of natural products biosynthesis, yet most clusters remain cryptic or down-regulated. Genome mining revealed an unconventional paraherquonin-like meroterpenoid biosynthetic gene cluster in the chromosome of Neosartorya glabra. The cryptic or down-regulated pathway was activated by constitutive expression of pathway-specific regulator gene berA encoded within ber biosynthetic gene cluster. Chemical analysis of mutant Ng-OE: berA extracts enabled the isolation of four berkeleyacetal congeners, in which two of them are new. On the basis of careful bioinformatic analysis of the coding enzymes in the ber gene cluster, the biosynthetic pathway of berkeleyacetals was proposed. These results indicate that this approach would be valuable for discovery of novel natural products and will accelerate the exploitation of prodigious natural products in filamentous fungi. (C) 2018 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:478 / 487
页数:10
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