Biosynthesis of the β-Lactone Proteasome Inhibitors Belactosin and Cystargolide

Angew Chem Int Ed Engl. 2017 Jun 1;56(23):6665-6668. doi: 10.1002/anie.201612076. Epub 2017 Apr 28.

Abstract

Belactosins and cystargolides are natural product proteasome inhibitors from Actinobacteria. Both feature dipeptidic backbones and a unique β-lactone building block. Herein, we present a detailed investigation of their biosynthesis. Identification and analysis of the corresponding gene clusters indicated that both compounds are assembled by rare single-enzyme amino acid ligases. Feeding experiments with isotope-labeled precursors and in vitro biochemistry showed that the formation of the β-lactone warhead is unprecedented and reminiscent of leucine biosynthesis, and that it involves the action of isopropylmalate synthase homologues.

Keywords: biosynthesis; inhibitors; lactones; metabolism; natural products.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / metabolism
  • Dipeptides / metabolism*
  • Genome, Bacterial
  • Intercellular Signaling Peptides and Proteins
  • Lactones / chemistry*
  • Ligases / genetics
  • Ligases / metabolism
  • Magnetic Resonance Spectroscopy
  • Multigene Family
  • Peptides / metabolism*
  • Proteasome Inhibitors / chemical synthesis*
  • Streptomycetaceae / genetics
  • Streptomycetaceae / metabolism*
  • Tandem Mass Spectrometry

Substances

  • Amino Acids
  • Dipeptides
  • Intercellular Signaling Peptides and Proteins
  • Lactones
  • Peptides
  • Proteasome Inhibitors
  • belactosin A
  • belactosin C
  • cystargolide A
  • cystargolide B
  • Ligases