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Antifungal cyclopeptolide from fungal saprophytic antagonist Ulocladium atrum.
Yun, Bong-Sik; Kwon, Eun Mi; Kim, Jin-Cheol; Yu, Seung Hun.
Affiliation
  • Yun BS; Functional Metabolomics Research Center, KRIBB, Daejeon 305-333, Korea.
J Microbiol Biotechnol ; 17(7): 1217-20, 2007 Jul.
Article in En | MEDLINE | ID: mdl-18051337
The saprophytic fungus Ulocladium atrum Preuss is a promising biological control agent for Botrytis cinerea in greenhouse- and field-grown crops. However, despite its known potent antifungal activity, no antifungal substance has yet been reported. In an effort to characterize the antifungal substance from U atrum, we isolated an antibiotic peptide. Based on extensive spectroscopic analyses, its structure was established as a cyclopeptolide with a high portion of N-methylated amino acids, and its 1H and 13C chemical shifts were completely assigned based on extensive 1D and 2D NMR experiments. Compound 1 exhibited potent antifungal activity against the plant pathogenic fungus Botrytis cinerea and moderate activity against Alternaria alternate and Magnaporthe grisea.
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Collection: 01-internacional Database: MEDLINE Main subject: Peptides, Cyclic / Ascomycota / Antifungal Agents Language: En Journal: J Microbiol Biotechnol Year: 2007 Document type: Article Country of publication: Korea (South)
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Peptides, Cyclic / Ascomycota / Antifungal Agents Language: En Journal: J Microbiol Biotechnol Year: 2007 Document type: Article Country of publication: Korea (South)