Substrate plasticity of dehydratase SpaKC from the biosynthesis of thiosparsoamide

J Pept Sci. 2022 Jun;28(6):e3388. doi: 10.1002/psc.3388. Epub 2021 Dec 20.

Abstract

Thioamitides are a group of ribosomally synthesized and post-translationally modified peptides that possess diverse bioactivities and are usually featured by thioamide and 2-aminovinyl-cysteine (AviCys) motifs. In natural product thiosparsoamide, the AviCys motif is formed by an enzyme cascade formed by the flavin-dependent decarboxylase SpaD and dehydratase SpaKC. SpaKC is a lanthipeptide synthetase homolog located outside the thiosparsoamide biosynthetic gene cluster. In this study, we show that SpaKC does not strictly require the N-terminal leader peptide of precursor peptide SpaA for substrate recognition and dehydration. The C-terminal seven residues serve as a minimal structural element for enzyme recognition. Through a systematic mutagenesis experiments, our study demonstrates the relaxed substrate specificity of SpaKC as a dehydratase and potentially as an enzymatic tool to install dehydroalanine or dehydrobutyrine motifs in peptides.

Keywords: RiPP; aminovinyl-cysteine; biosynthesis; dehydratase; thioamitide.

MeSH terms

  • Cysteine* / chemistry
  • Hydro-Lyases / genetics
  • Peptides* / chemistry
  • Protein Processing, Post-Translational
  • Substrate Specificity
  • Thioamides

Substances

  • Peptides
  • Thioamides
  • Hydro-Lyases
  • Cysteine