Marine Drugs (Jun 2017)

Borrelidins C–E: New Antibacterial Macrolides from a Saltern-Derived Halophilic Nocardiopsis sp.

  • Jungwoo Kim,
  • Daniel Shin,
  • Seong-Hwan Kim,
  • Wanki Park,
  • Yoonho Shin,
  • Won Kyung Kim,
  • Sang Kook Lee,
  • Ki-Bong Oh,
  • Jongheon Shin,
  • Dong-Chan Oh

DOI
https://doi.org/10.3390/md15060166
Journal volume & issue
Vol. 15, no. 6
p. 166

Abstract

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Chemical investigation of a halophilic actinomycete strain belonging to the genus Nocardiopsis inhabiting a hypersaline saltern led to the discovery of new 18-membered macrolides with nitrile functionality, borrelidins C–E (1–3), along with a previously reported borrelidin (4). The planar structures of borrelidins C–E, which are new members of the rare borrelidin class of antibiotics, were elucidated by NMR, mass, IR, and UV spectroscopic analyses. The configurations of borrelidines C–E were determined by the interpretation of ROESY NMR spectra, J-based configuration analysis, a modified Mosher’s method, and CD spectroscopic analysis. Borrelidins C and D displayed inhibitory activity, particularly against the Gram-negative pathogen Salmonella enterica, and moderate cytotoxicity against the SNU638 and K562 carcinoma cell lines.

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