4.6 Article

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

期刊

GENE
卷 546, 期 2, 页码 352-358

出版社

ELSEVIER
DOI: 10.1016/j.gene.2014.05.053

关键词

Streptomyces sp.; Nonribosomal peptide synthetase; Quinone synthetase; Echosides; Biosynthesis

资金

  1. 973 Programs [2010CB833802, 2012CB721005]
  2. National Natural Science Foundation of China [31100079]
  3. Program for Changjiang Scholars and Innovative Research Team in University [IRT13028]

向作者/读者索取更多资源

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.

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