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Identification and catalytic characterization of a nonribosomal peptide synthetase-like (NRPS-like) enzyme involved in the biosynthesis of echosides from Streptomyces sp. LZ35.
Zhu, Jing; Chen, Wang; Li, Yao-Yao; Deng, Jing-Jing; Zhu, De-Yu; Duan, Jing; Liu, Yi; Shi, Guo-Yin; Xie, Chao; Wang, Hao-Xin; Shen, Yue-Mao.
Afiliação
  • Zhu J; State Key Laboratory of Microbial Technology, School of Life Science, Shandong University, Jinan 250100, PR China.
  • Chen W; Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Shandong University, Jinan, Shandong 250012, PR China.
  • Li YY; Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Shandong University, Jinan, Shandong 250012, PR China.
  • Deng JJ; Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Shandong University, Jinan, Shandong 250012, PR China.
  • Zhu DY; State Key Laboratory of Microbial Technology, School of Life Science, Shandong University, Jinan 250100, PR China.
  • Duan J; State Key Laboratory of Microbial Technology, School of Life Science, Shandong University, Jinan 250100, PR China.
  • Liu Y; State Key Laboratory of Microbial Technology, School of Life Science, Shandong University, Jinan 250100, PR China.
  • Shi GY; State Key Laboratory of Microbial Technology, School of Life Science, Shandong University, Jinan 250100, PR China.
  • Xie C; State Key Laboratory of Microbial Technology, School of Life Science, Shandong University, Jinan 250100, PR China.
  • Wang HX; State Key Laboratory of Microbial Technology, School of Life Science, Shandong University, Jinan 250100, PR China. Electronic address: wanghaoxin@sdu.edu.cn.
  • Shen YM; State Key Laboratory of Microbial Technology, School of Life Science, Shandong University, Jinan 250100, PR China; Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Shandong University, Jinan, Shandong 250012, PR China. Electronic address: yshen@sdu.edu.c
Gene ; 546(2): 352-8, 2014 Aug 10.
Article em En | MEDLINE | ID: mdl-24865933
Echosides, isolated from Streptomyces sp. LZ35, represent a class of para-terphenyl natural products that display DNA topoisomerase I and IIα 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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeo Sintases / Streptomyces / Compostos de Terfenil / Proteínas de Bactérias Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeo Sintases / Streptomyces / Compostos de Terfenil / Proteínas de Bactérias Idioma: En Ano de publicação: 2014 Tipo de documento: Article