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.
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Chiou, C. C., Mavrogiorgos, N., Tillem, E., Hector, R. & Walsh, T. J. Synergy, pharmacodynamics, and time-sequenced ultrastructural changes of the interaction between nikkomycin Z and the echinocandin FK463 against Aspergillus fumigatus. Antimicrob. Agents Chemother. 45, 3310–3321 (2001).
Clemons, K. V. & Stevens, D. A. Efficacy of micafungin alone or in combination against experimental pulmonary aspergillosis. Med. Mycol. 44, 69–73 (2006).
Kato, A. et al. A new anti-MRSA antibiotic complex, WAP-8294A. I. Taxonomy, isolation and biological activities. J. Antibiot. 51, 929–935 (1998).
Fujie, A. et al. FR901469, a novel antifungal antibiotic from an unidentified fungus No.11243. I. Taxonomy, fermentation, isolation, physico-chemical properties and biological properties. J. Antibiot. 53, 912–919 (2000).
Fujie, A. et al. FR901469, a novel antifungal antibiotic from an unidentified fungus No.11243. II. In vitro and in vivo activities. J. Antibiot. 53, 920–927 (2000).
Tawara, S. et al. In vitro activities of a new lipopeptide antifungal agent, FK463, against a variety of clinically important fungi. Antimicrob. Agents Chemother. 44, 57–62 (2000).
Debono, M. & Gordee, R. S. Antibiotics that inhibit fungal cell wall development. Annu. Rev. Microbiol. 48, 471–497 (1994).
Liu, J. & Balasubramanian, M. K. 1,3-beta-Glucan synthase: a useful target for antifungal drugs. Curr. Drug Targets Infect. Disord. 1, 159–169 (2001).
Kai, H. et al. KB425796-A, a novel antifungal antibiotic produced by Paenibacillus sp. 530603. J. Antibiot. 66, 465–471 (2013).
Matsubara, H. & Sasaki, R. M. High recovery of tryptophan from acid hydrolysates of proteins. Biochem. Biophys. Res. Commun. 35, 175–181 (1969).
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Kai, H., Yamashita, M., Takase, S. et al. Identification of ten KB425796-A congeners from Paenibacillus sp. 530603 using an antifungal assay against Aspergillus fumigatus in combination with micafungin. J Antibiot 66, 473–478 (2013). https://doi.org/10.1038/ja.2013.64
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DOI: https://doi.org/10.1038/ja.2013.64