The biosynthetic pathway to ossamycin, a macrocyclic polyketide bearing a spiroacetal moiety

PLoS One. 2019 Apr 30;14(4):e0215958. doi: 10.1371/journal.pone.0215958. eCollection 2019.

Abstract

Ossamycin from Streptomyces hygroscopicus var. ossamyceticus is an antifungal and cytotoxic polyketide and a potent inhibitor of the mitochondrial ATPase. Analysis of a near-complete genome sequence of the ossamycin producer has allowed the identification of the 127-kbp ossamycin biosynthetic gene cluster. The presence in the cluster of a specific crotonyl-CoA carboxylase/reductase homologue suggests that the 5-methylhexanoate extension unit used in construction of the macrocyclic core is incorporated intact from the unusual precursor isobutyrylmalonyl-CoA. Surprisingly, the modular polyketide synthase uses only 14 extension modules to accomplish 15 cycles of polyketide chain extension, a rare example of programmed iteration on a modular polyketide synthase. Specific deletion of genes encoding cytochrome P450 enzymes has given insight into the late-stage tailoring of the ossamycin macrocycle required for the attachment of the unusual 2,3,4,6-deoxyaminohexose sugar l-ossamine to C-8 of the ossamycin macrocycle. The ossamycin cluster also encodes a putative spirocyclase enzyme, OssO, which may play a role in establishing the characteristic spiroketal moiety of the natural product.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biosynthetic Pathways* / genetics
  • Cytochrome P-450 Enzyme System / metabolism
  • Genes, Bacterial
  • Macrolides / chemistry*
  • Macrolides / metabolism*
  • Multigene Family
  • Polyketide Synthases / genetics
  • Spiro Compounds / chemistry*
  • Streptomyces / genetics

Substances

  • Macrolides
  • Spiro Compounds
  • ossamycin
  • Polyketide Synthases
  • Cytochrome P-450 Enzyme System

Grants and funding

The authors gratefully acknowledge funding from the Herchel Smith Chair of Biochemistry Fund, University of Cambridge, to PFL, and an EU Marie Skłodowska-Curie Fellowship (CaLiAT, project 705690) awarded to OB. The funders had no role in study design, data collection and analysis, decision to publish, or preraration of the manuscript.