The role of acyl-coenzyme A carboxylase complex in lipstatin biosynthesis of Streptomyces toxytricini

Appl Microbiol Biotechnol. 2010 Jul;87(3):1129-39. doi: 10.1007/s00253-010-2587-2. Epub 2010 May 2.

Abstract

Streptomyces toxytricini produces lipstatin, a specific inhibitor of pancreatic lipase, which is derived from two fatty acid moieties with eight and 14 carbon atoms. The pccB gene locus in 10.6 kb fragment of S. toxytricini chromosomal DNA contains three genes for acyl-coenzyme A carboxylase (ACCase) complex accA3, pccB, and pccE that are presumed to be involved in secondary metabolism. The pccB gene encoding a beta subunit of ACCase [carboxyltransferase (CT)] was identified upstream of pccE gene for a small protein of epsilon subunit. The accA3 encoding the alpha subunit of ACCase [biotin carboxylase (BC)] was also identified downstream of pccB gene. When the pccB and pccE genes were inactivated by homologous recombination, the lipstatin production was reduced as much as 80%. In contrast, the accumulation of another compound, tetradeca-5.8-dienoic acid (the major lipstatin precursor), was 4.5-fold increased in disruptant compared with wild-type. It implies that PccB of S. toxytricini is involved in the activation of octanoic acid to hexylmalonic acid for lipstatin biosynthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Bacterial Proteins / chemistry
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Biosynthetic Pathways
  • Carbon-Carbon Ligases / chemistry
  • Carbon-Carbon Ligases / genetics
  • Carbon-Carbon Ligases / metabolism*
  • Lactones / metabolism*
  • Molecular Sequence Data
  • Protein Subunits / genetics
  • Protein Subunits / metabolism
  • Sequence Alignment
  • Streptomyces / chemistry
  • Streptomyces / enzymology
  • Streptomyces / genetics
  • Streptomyces / metabolism

Substances

  • Bacterial Proteins
  • Lactones
  • Protein Subunits
  • lipstatin
  • Carbon-Carbon Ligases
  • acyl-CoA carboxylase