Discovery of a new source of rifamycin antibiotics in marine sponge actinobacteria by phylogenetic prediction

Appl Environ Microbiol. 2006 Mar;72(3):2118-25. doi: 10.1128/AEM.72.3.2118-2125.2006.

Abstract

Phylogenetic analysis of the ketosynthase (KS) gene sequences of marine sponge-derived Salinispora strains of actinobacteria indicated that the polyketide synthase (PKS) gene sequence most closely related to that of Salinispora was the rifamycin B synthase of Amycolatopsis mediterranei. This result was not expected from taxonomic species tree phylogenetics using 16S rRNA sequences. From the PKS sequence data generated from our sponge-derived Salinispora strains, we predicted that such strains might synthesize rifamycin-like compounds. Liquid chromatography-tandem mass spectrometry (LC/MS/MS) analysis was applied to one sponge-derived Salinispora strain to test the hypothesis of rifamycin synthesis. The analysis reported here demonstrates that this Salinispora isolate does produce compounds of the rifamycin class, including rifamycin B and rifamycin SV. A rifamycin-specific KS primer set was designed, and that primer set increased the number of rifamycin-positive strains detected by PCR screening relative to the number detectable using a conserved KS-specific set. Thus, the Salinispora group of actinobacteria represents a potential new source of rifamycins outside the genus Amycolatopsis and the first recorded source of rifamycins from marine bacteria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actinomycetales / enzymology
  • Actinomycetales / genetics
  • Actinomycetales / metabolism*
  • Amino Acid Sequence
  • Animals
  • Anti-Bacterial Agents / metabolism*
  • DNA, Ribosomal / analysis
  • Molecular Sequence Data
  • Phylogeny*
  • Polyketide Synthases / chemistry
  • Polyketide Synthases / genetics*
  • Polyketide Synthases / metabolism
  • Polymerase Chain Reaction / methods
  • Porifera / microbiology*
  • RNA, Ribosomal, 16S / genetics
  • Rifamycins / chemistry
  • Rifamycins / metabolism*
  • Sequence Alignment

Substances

  • Anti-Bacterial Agents
  • DNA, Ribosomal
  • RNA, Ribosomal, 16S
  • Rifamycins
  • Polyketide Synthases