Cyclic heptapeptide microcystin biosynthesis requires the glutamate racemase gene

Microbiology (Reading). 2001 May;147(Pt 5):1235-1241. doi: 10.1099/00221287-147-5-1235.

Abstract

It was demonstrated previously that the operon consisting of the non-ribosomal peptide synthetase (NRPS) gene coupled with the polyketide synthase (PKS) gene involved in cyclic heptapeptide microcystin synthesis includes two different D-amino acid synthetase genes, an epimerization domain at the 3' end of module 2, and the racemase gene mcyF. To determine the role of mcyF in microcystin synthesis, gene-disruption and complementation analyses were carried out. Insertional mutagenesis in the mcyF gene, generated by homologous recombination, abolished only microcystin synthesis, but did not influence cell growth. Furthermore, McyF supported D-Glu-independent growth of a strain of Escherichia coli defective in D-Glu synthesis. It is concluded that mcyF is the glutamic acid racemase gene involved in the synthesis of D-Glu residues in the microcystin molecule. This is the first report of the racemase in prokaryotic NRPS.

MeSH terms

  • Amino Acid Isomerases / genetics*
  • Amino Acid Isomerases / metabolism
  • Chromatography, High Pressure Liquid
  • Cyanobacteria / genetics*
  • Cyanobacteria / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Genetic Complementation Test
  • Glutamic Acid / biosynthesis
  • Microcystins
  • Mutagenesis, Insertional
  • Operon
  • Peptide Synthases / genetics*
  • Peptide Synthases / metabolism
  • Peptides, Cyclic / metabolism*
  • Phylogeny
  • Recombinant Proteins / metabolism

Substances

  • Microcystins
  • Peptides, Cyclic
  • Recombinant Proteins
  • Glutamic Acid
  • microcystin
  • Amino Acid Isomerases
  • glutamate racemase
  • Peptide Synthases
  • non-ribosomal peptide synthase