Broad substrate specificity of the loading didomain of the lipomycin polyketide synthase

Biochemistry. 2013 Jun 4;52(22):3791-3. doi: 10.1021/bi400520t. Epub 2013 May 23.

Abstract

LipPks1, a polyketide synthase subunit of the lipomycin synthase, is believed to catalyze the polyketide chain initiation reaction using isobutyryl-CoA as a substrate, followed by an elongation reaction with methylmalonyl-CoA to start the biosynthesis of antibiotic α-lipomycin in Streptomyces aureofaciens Tü117. Recombinant LipPks1, containing the thioesterase domain from the 6-deoxyerythronolide B synthase, was produced in Escherichia coli, and its substrate specificity was investigated in vitro. Surprisingly, several different acyl-CoAs, including isobutyryl-CoA, were accepted as the starter substrates, while no product was observed with acetyl-CoA. These results demonstrate the broad substrate specificity of LipPks1 and may be applied to producing new antibiotics.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acyl Coenzyme A / metabolism*
  • Escherichia coli / enzymology
  • Glycosides / biosynthesis
  • Polyenes
  • Polyketide Synthases / chemistry
  • Polyketide Synthases / metabolism*
  • Protein Structure, Tertiary
  • Streptomyces aureofaciens / enzymology
  • Substrate Specificity

Substances

  • Acyl Coenzyme A
  • Glycosides
  • Polyenes
  • alpha-lipomycin
  • methylmalonyl-coenzyme A
  • Polyketide Synthases