4.8 Article

Biosynthetic Origins of the Ionophore Antibiotic Indanomycin

Journal

ORGANIC LETTERS
Volume 11, Issue 2, Pages 297-300

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol802422n

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Funding

  1. Georgia Institute of Technology
  2. Camille and Henry Dreyfus Foundation

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The pyrroloketoindane antibiotic indanomycin is produced by Streptomyces antibioticus NRRL 8167. These hybrid nonribosomal peptide-polyketide ionophore antibiotics are characterized by the presence of an unusual indane ring system, and there is interest in identifying the biochemical mechanisms guiding its biosynthesis. Following incorporation of [1-C-13]-labeled precursors, the primary metabolic origins of indanomycin were determined to be one unit Of L-proline, six units of malonyl-CoA and two units each of methylmalonyl-CoA and ethylmalonyl-CoA.

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