Complete sequence of biosynthetic gene cluster responsible for producing triostin A and evaluation of quinomycin-type antibiotics from Streptomyces triostinicus

Biotechnol Prog. 2008 Nov-Dec;24(6):1226-31. doi: 10.1002/btpr.34.

Abstract

Streptomyces triostinicus produces triostin A, an antitumor antibiotic, as its major secondary metabolite. Surprisingly, this strain also produced a trace amount of echinomycin. We sequenced the entire triostin A biosynthetic gene cluster from S. triostinicus, and found that this 36 kilobase-long gene cluster contained an ORF homologous to ecm18 that encodes a thioacetal-forming enzyme responsible for the triostin A-to-echinomycin bioconversion. These findings indicate that, unlike previously thought, S. triostinicus is capable of producing not only triostin A but also echinomycin. Our observation suggests potential value in careful re-analysis for metabolites from previously characterized natural product producers with the current technologies.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / biosynthesis*
  • Anti-Bacterial Agents / chemistry
  • Base Sequence
  • Biosynthetic Pathways
  • Cloning, Molecular
  • Echinomycin / biosynthesis*
  • Echinomycin / chemistry
  • Genomic Library
  • Molecular Conformation
  • Molecular Sequence Data
  • Multigene Family / genetics*
  • Quinoxalines / chemistry
  • Quinoxalines / metabolism
  • Sequence Analysis, DNA
  • Streptomyces / genetics
  • Streptomyces / metabolism*

Substances

  • Anti-Bacterial Agents
  • Quinoxalines
  • triostin A
  • Echinomycin

Associated data

  • GENBANK/AB366635
  • GENBANK/AB369992