Insights into the pamamycin biosynthesis

Angew Chem Int Ed Engl. 2015 Feb 9;54(7):2280-4. doi: 10.1002/anie.201408901. Epub 2014 Dec 23.

Abstract

Pamamycins are macrodiolides of polyketide origin with antibacterial activities. Their biosynthesis has been proposed to utilize succinate as a building block. However, the mechanism of succinate incorporation into a polyketide was unclear. Here, we report identification of a pamamycin biosynthesis gene cluster by aligning genomes of two pamamycin-producing strains. This unique cluster contains polyketide synthase (PKS) genes encoding seven discrete ketosynthase (KS) enzymes and one acyl-carrier protein (ACP)-encoding gene. A cosmid containing the entire set of genes required for pamamycin biosynthesis was successfully expressed in a heterologous host. Genetic and biochemical studies allowed complete delineation of pamamycin biosynthesis. The pathway proceeds through 3-oxoadipyl-CoA, a key intermediate in the primary metabolism of the degradation of aromatic compounds. 3-Oxoadipyl-CoA could be used as an extender unit in polyketide assembly to facilitate the incorporation of succinate.

Keywords: Streptomyces; biosynthesis; polyketide synthase; polyketides; succinate.

MeSH terms

  • Acyl Carrier Protein / genetics
  • Acyl Carrier Protein / metabolism*
  • Anti-Bacterial Agents / metabolism*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Biosynthetic Pathways
  • Macrolides / metabolism*
  • Multigene Family
  • Polyketide Synthases / genetics
  • Polyketide Synthases / metabolism*
  • Streptomyces / genetics
  • Streptomyces / metabolism*

Substances

  • Acyl Carrier Protein
  • Anti-Bacterial Agents
  • Bacterial Proteins
  • Macrolides
  • pamamycin
  • Polyketide Synthases