Bonnevillamides, Linear Heptapeptides Isolated from a Great Salt Lake-Derived Streptomyces sp

Mar Drugs. 2017 Jun 24;15(7):195. doi: 10.3390/md15070195.

Abstract

Streptomyces sp. GSL-6B was isolated from sediment collected from the Great Salt Lake and investigation of its organic extract led to the isolation of three new linear heptapeptides, bonnevillamides A (1), B (2), and C (3). The bonnevillamides represent a new class of linear peptides featuring unprecedented non-proteinogenic amino acids. All three peptides contain the newly characterized bonnevillic acid moiety (3-(3,5-dichloro-4-methoxyphenyl)-2-hydroxyacrylic acid), as well as a heavily modified proline residue. Moreover, in bonnevillamide A, the terminal proline residue found in bonnevillamides B and C is replaced with 4-methyl-azetidine-2-carboxylic acid methyl ester. The structures of the three heptapeptides were elucidated by NMR, high-resolution electrospray ionization mass spectroscopy (HRESIMS), and LC-MS/MS, and the absolute configuration of all proteinogenic amino acid residues were determined by advanced Marfey's method. Bonnevillamides A, B and C were evaluated for their effects on zebrafish embryo development. All three heptapeptides were shown to modulate heart growth and cardiac function, with bonnevillamide B having the most pronounced effect.

Keywords: Great Salt Lake; Streptomyces sp.; azetidine; heptapeptide; hypersaline environment; zebrafish.

MeSH terms

  • Animals
  • Dose-Response Relationship, Drug
  • Embryo, Nonmammalian / drug effects
  • Lakes / chemistry
  • Larva / drug effects
  • Models, Molecular
  • Molecular Structure
  • Peptides / chemistry*
  • Peptides / metabolism
  • Streptomyces / metabolism*
  • Utah
  • Zebrafish

Substances

  • Peptides