Function analysis of a new type I PKS-SAT domain by SAT-EAT domain replacement

Prikl Biokhim Mikrobiol. 2010 Mar-Apr;46(2):161-5.

Abstract

The function of a new starter unit acyltransferase (SAT) domain SAT-EF080951 (GenBank accession number) encoded in a new type I polyketide synthase (PKS) gene cluster EF568935 (GenBank accession number) isolated for this study was analyzed by domain replacement with an extender unit AT (EAT) domain of avermectin PKS. It was shown that the SAT-EF080951 incorporated malonyl-CoA specifically in vivo, which contradicted the specificity that we had previously determined by substrate binding test in vitro. The result of this study indicates that type I PKS-SAT can alter its specificity in vivo and functions well in extender units and proved the feasibility of the SAT-EAT domain replacement in type I PKS. We propose that SAT-EAT replacement strategy could be a novel route for increasing the diversity of new polyketides combinatorially biosynthesized. The new type I PKS-SAT-EF080951 studied herein may be further employed for related studies on enzymology or combinatorial biosynthesis of polyketides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyltransferases / chemistry
  • Acyltransferases / genetics
  • Acyltransferases / metabolism*
  • Catalytic Domain*
  • Combinatorial Chemistry Techniques
  • Ivermectin / analogs & derivatives
  • Ivermectin / metabolism
  • Macrolides / metabolism
  • Metagenome
  • Mutation
  • Polyketide Synthases / chemistry
  • Polyketide Synthases / genetics
  • Polyketide Synthases / metabolism*
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Streptomyces / genetics
  • Transformation, Bacterial

Substances

  • Macrolides
  • Recombinant Proteins
  • Ivermectin
  • avermectin
  • Polyketide Synthases
  • Acyltransferases