Synthesis of the reported structure of homocereulide and its vacuolation assay

Bioorg Med Chem Lett. 2019 Mar 1;29(5):734-739. doi: 10.1016/j.bmcl.2019.01.007. Epub 2019 Jan 10.

Abstract

Homocereulide, isolated from marine bacterium Bacillus cereus, is an analog of emetic toxin cereulide. There is no report on its structure determination and involvement in B. cereus-associated food poisoning. Homocereulide is a cyclic dodecadepsipeptide composed of l-O-Val-l-Val-d-O-Leu-d-Ala and l-O-allo-Ile-d-Val-d-O-Leu-d-Ala. Here, we synthesized homocereulide using liquid phase fragment condensation. The NMR spectrum of synthesized homocereulide confirmed the intended structure and LC-MS results were consistent with natural products. Morphological evaluation using HEp-2 cells showed higher toxicity with homocereulide (1.39 nM) than cereulide (3.95 nM). Though cereulide is the main component in broth culture, homocereulide is also likely involved in B. cereus-associated food poisoning.

Keywords: Bacillus cereus; Cereulide analogs; Emetic toxin; Homocereulide; Total synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacillus cereus / metabolism*
  • Chromatography, Liquid / methods
  • Depsipeptides / chemistry
  • Depsipeptides / metabolism*
  • Magnetic Resonance Spectroscopy / methods
  • Mass Spectrometry / methods
  • Vacuoles / chemistry*

Substances

  • Depsipeptides
  • cereulide