Genotype-driven isolation of enterocin with novel bioactivities from mangrove-derived Streptomyces qinglanensis 172205

Appl Microbiol Biotechnol. 2015 Jul;99(14):5825-32. doi: 10.1007/s00253-015-6574-5. Epub 2015 Apr 17.

Abstract

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 (3-5) 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid beta-Peptides / antagonists & inhibitors
  • Antineoplastic Agents / metabolism
  • Biosynthetic Pathways / genetics*
  • Bridged-Ring Compounds / isolation & purification
  • Bridged-Ring Compounds / metabolism
  • Cell Survival / drug effects
  • Environmental Microbiology
  • Genotype*
  • HeLa Cells
  • Hep G2 Cells
  • Humans
  • Streptomyces / genetics*
  • Streptomyces / isolation & purification
  • Streptomyces / metabolism*
  • Tandem Mass Spectrometry

Substances

  • Amyloid beta-Peptides
  • Antineoplastic Agents
  • Bridged-Ring Compounds
  • enterocin