Cloning and characterization of the gene cluster required for beauvericin biosynthesis in Fusarium proliferatum

被引:23
作者
Zhang Tao [1 ,2 ]
Zhuo Ying [1 ]
Jia XiaoPeng [1 ,2 ]
Liu JinTao [1 ,2 ]
Gao Hong [1 ]
Song FuHang [1 ]
Liu Mei [1 ]
Zhang LiXin [1 ]
机构
[1] Chinese Acad Sci, Inst Microbiol, CAS Key Lab Pathogen Microbiol & Immunol, Beijing 100101, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
beauvericin; Fusarium proliferatum; biosynthesis gene cluster; synthetic biology; DEPSIPEPTIDE BEAUVERICIN; ENNIATIN SYNTHETASE; VIRULENCE FACTOR; WEB SERVER; PREDICTION; BASSIANOLIDE; POLYKETIDE; AUGUSTUS; DOMAINS;
D O I
10.1007/s11427-013-4505-1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Beauvericin, a cyclohexadepsipeptide-possessing natural product with synergistic antifungal, insecticidal, and cytotoxic activities. We isolated and characterized the fpBeas gene cluster, devoted to beauvericin biosynthesis, from the filamentous fungus Fusarium proliferatum LF061. Targeted inactivation of the F. proliferatum genomic copy of fpBeas abolished the production of beauvericin. Comparative sequence analysis of the FpBEAS showed 74% similarity with the BbBEAS that synthesizes the cyclic trimeric ester beauvericin in Beauveria bassiana, which assembles N-methyl-dipeptidol monomer intermediates by the programmed iterative use of the nonribosomal peptide synthetase modules. Differences between the organization of the beauvericin loci in F. proliferaturm and B. bassiana revealed the mechanism for high production of beauvericin in F. proliferatum. Our work provides new insights into beauvericin biosynthesis, and may lead to beauvericin overproduction and creation of new analogs via synthetic biology approaches.
引用
收藏
页码:628 / 637
页数:10
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