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Phellinsin A, a novel chitin synthases inhibitor produced by Phellinus sp. PL3

  • E. I. Hwang
  • , B. S. Yun
  • , Y. K. Kim
  • , B. M. Kwon
  • , H. G. Kim
  • , H. B. Lee
  • , W. J. Jeong
  • , S. U. Kim*
  • *Corresponding author for this work
  • Korea Research Institute of Bioscience and Biotechnology

Research output: Contribution to journalJournal articlepeer-review

Abstract

Phellinsin A, a novel chitin synthases inhibitor was isolated from the cultured broth of fungus PL3, which was identified as Phellinus sp. PL3. Phellinsin A was purified by solvent partition, silica gel, ODS column chromatographies, and preparative HPLC, consecutively. The structure of phellinsin A was assigned as a phenolic compound on the basis of various spectroscopic analyses including UV, IR, Mass, and NMR. Its molecular weight and formula were found to be 358 and C18H14O8, respectively. Phellinsin A selectively inhibited chitin synthase I and II of Saccharomyces cerevisiae with an IC50 value of 76 and 28 μg/ml, respectively, in our cell free assay system. This compound showed antifungal activity against Colletotrichum lagenarium, Pyricularia oryzae, Rhizoctonia solani, Aspergillus fumigatus, and Trichophyton mentagrophytes.

Original languageEnglish
Pages (from-to)903-911
Number of pages9
JournalJournal of Antibiotics
Volume53
Issue number9
DOIs
StatePublished - 2000

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