Identification of ten KB425796-A congeners from Paenibacillus sp. 530603 using an antifungal assay against Aspergillus fumigatus in combination with micafungin

J Antibiot (Tokyo). 2013 Aug;66(8):473-8. doi: 10.1038/ja.2013.64. Epub 2013 Jun 19.

Abstract

The discovery and characterization of natural congeners is one approach for understanding the relationship between chemical structure and biological function. We recently isolated the novel antifungal metabolite KB425796-A produced by the recently isolated bacterium Paenibacillus sp. 530603. On the basis of morphological changes of Aspergillus fumigatus induced by KB425796-A in combination with micafungin, we developed a highly sensitive screening method for the specific detection of KB425796-A congeners. Using this method, we isolated ten congeners of KB425796-A, named KB425796-B, -C, -D, -E, -F, -G, -H, -I, -J and -K, which exhibited diverse antifungal potencies against A. fumigatus. One of the most potent congeners, KB425796-C, had antifungal activities against several micafungin-resistant infectious fungi. KB425796-C can be a potential drug candidate for treating micafungin-resistant fungal infections.

Publication types

  • Comparative Study

MeSH terms

  • Antifungal Agents / chemistry
  • Antifungal Agents / isolation & purification
  • Antifungal Agents / pharmacology*
  • Aspergillus fumigatus / drug effects*
  • Depsipeptides / chemistry
  • Depsipeptides / isolation & purification
  • Depsipeptides / pharmacology*
  • Drug Resistance, Fungal
  • Drug Therapy, Combination
  • Echinocandins / pharmacology*
  • Lipopeptides / pharmacology*
  • Micafungin
  • Microbial Sensitivity Tests
  • Paenibacillus / metabolism

Substances

  • Antifungal Agents
  • Depsipeptides
  • Echinocandins
  • KB425796-A
  • Lipopeptides
  • Micafungin