Prerequisites of Isopeptide Bond Formation in Microcystin Biosynthesis

Chembiochem. 2017 Dec 14;18(24):2376-2379. doi: 10.1002/cbic.201700389. Epub 2017 Oct 27.

Abstract

The biosynthesis of the potent cyanobacterial hepatotoxin microcystin involves isopeptide bond formation through the carboxylic acid side chains of d-glutamate and β-methyl d-aspartate. Analysis of the in vitro activation profiles of the two corresponding adenylation domains, McyE-A and McyB-A2 , either in a didomain or a tridomain context with the cognate thiolation domain and the upstream condensation domain revealed that substrate activation of both domains strictly depended on the presence of the condensation domains. We further identified two key amino acids in the binding pockets of both adenylation domains that could serve as a bioinformatic signature of isopeptide bond-forming modules incorporating d-glutamate or d-aspartate. Our findings further contribute to the understanding of the multifaceted role of condensation domains in nonribosomal peptide synthetase assembly lines.

Keywords: amino acids; biosynthesis; cyanobacteria; nonribosomal peptide; substrate specificity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Monophosphate / chemistry
  • Binding Sites
  • Cyanobacteria / chemistry
  • Cyanobacteria / enzymology
  • Cyanobacteria / metabolism*
  • D-Aspartic Acid / chemistry
  • Glutamic Acid / chemistry
  • Microcystins / biosynthesis*
  • Peptide Biosynthesis, Nucleic Acid-Independent*
  • Protein Domains

Substances

  • Microcystins
  • Glutamic Acid
  • Adenosine Monophosphate
  • D-Aspartic Acid