4.7 Article

Identification of Elaiophylin Derivatives from the Marine-Derived Actinomycete Streptomyces sp 7-145 Using PCR-Based Screening

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 76, Issue 11, Pages 2153-2157

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/np4006794

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Funding

  1. Natural Sciences Foundation of China (NSFC) [81273414, 81001386]
  2. Beijing Natural Science Foundation [5122032]
  3. National Science and Technology Project of China [2014ZX09507009-008, 2012ZX09301002-003]

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A PCR-based genetic screening experiment targeting the dTDP-glucose-4,6-dehydratase gene revealed that a marine sediment-derived strain, Streptomyces sp. 7-145, had the potential to produce glycosidic antibiotics. Chemical investigation of culture extracts of this strain yielded two new 6-deoxyhexose-containing antibiotics, 11',12'-dehydroelaiophylin (1) and 11,11'-O-dimethyl-14'-deethyl-14'-methylelaiophylin (2), together with four known elaiophylin analogues (3-6). Their structures were determined by extensive NMR, MS, and CD analyses. Compounds 1, 3, 4, and 6 showed good antibacterial activity against methicillin-resistant Staphylococcus aureus and vancomycin-resistant enterococci pathogens.

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