Genotype-driven isolation of enterocin with novel bioactivities from mangrove-derived Streptomyces qinglanensis 172205
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  • 作者:Dong-Bo Xu ; Min Ma ; Zi-Xin Deng ; Kui Hong
  • 关键词:Enterocin ; Genome ; Mass spectrometry ; Starter units ; Aβ1 ; 42 fibrillation ; Cytotoxicity
  • 刊名:Applied Microbiology and Biotechnology
  • 出版年:2015
  • 出版时间:July 2015
  • 年:2015
  • 卷:99
  • 期:14
  • 页码:5825-5832
  • 全文大小:991 KB
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  • 作者单位:Dong-Bo Xu (1)
    Min Ma (1)
    Zi-Xin Deng (1)
    Kui Hong (1)

    1. Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, School of Pharmaceutical Sciences, Wuhan University, Wuhan, 430071, China
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Biotechnology
    Microbiology
    Microbial Genetics and Genomics
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1432-0614
文摘
The type II polyketide synthase (PKS) natural product enterocin (1) was isolated from a mangrove-derived novel species Streptomyces qinglanensis 172205 guided by genome sequence, and its putative biosynthetic gene cluster was revealed. Its natural analogues 5-deoxyenterocin (2) and wailupemycin A–C (3-) were also identified by tandem mass spectrometry. By feeding experiments with aryl acids, strain 172205 was proved to incorporate partial exogenous starter units into enterocin- and wailupemycin-based analogues, thus being a new and suitable microorganism for engineering unnatural enc-derived polyketide metabolites. In addition, biological assays indicated that enterocin showed obvious inhibitory activity against β-amyloid protein (Aβ1-42) fibrillation and moderate cytotoxicity against HeLa and HepG2 for the first time.

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