Identification and catalytic characterization of a nonribosomal peptide synthetase-like (NRPS-like) enzyme involved in the biosynthesis of echosides from Streptomyces sp LZ35

被引:33
作者
Zhu, Jing [1 ]
Chen, Wang [2 ]
Li, Yao-Yao [2 ]
Deng, Jing-Jing [2 ]
Zhu, De-Yu [1 ]
Duan, Jing [1 ]
Liu, Yi [1 ]
Shi, Guo-Yin [1 ]
Xie, Chao [1 ]
Wang, Hao-Xin [1 ]
Shen, Yue-Mao [1 ,2 ]
机构
[1] Shandong Univ, Sch Life Sci, State Key Lab Microbial Technol, Jinan 250100, Peoples R China
[2] Shandong Univ, Sch Pharmaceut Sci, Key Lab Chem Biol, Minist Educ, Jinan 250012, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Streptomyces sp; Nonribosomal peptide synthetase; Quinone synthetase; Echosides; Biosynthesis; NAPHTHOQUINONE ANSAMYCINS; ATROMENTIN; INHIBITOR; HYGROCINS; GENES; DNA;
D O I
10.1016/j.gene.2014.05.053
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Echosides, isolated from Streptomyces sp.LZ35, represent a class of para-terphenyl natural products that display DNA topoisomerase I and II alpha inhibitory activities. By analyzing the genome draft of strain LZ35, the ech gene cluster was identified to be responsible for the biosynthesis of echosides, which was further confirmed by gene disruption and HPLC analysis. Meanwhile, the biosynthetic pathway for echosides was proposed. Furthermore, the echA-gene, encoding a tri-domain nonribosomal peptide synthetase (NRPS)-like enzyme, was identified as a polyporic acid synthetase and biochemically characterized in vitro. This is the first study to our knowledge on the biochemical characterization of an Actinobacteria quinone synthetase, which accepts phenylpyruvic acid as a native substrate. Therefore, our results may help investigate the function of other NRPS-like enzymes in Actinobacteria. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:352 / 358
页数:7
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