This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wicklow, D. T.
Right arrow Articles by Dowd, P. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wicklow, D. T.
Right arrow Articles by Dowd, P. F.
Agricola
Right arrow Articles by Wicklow, D. T.
Right arrow Articles by Dowd, P. F.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, November 1998, p. 4482-4484, Vol. 64, No. 11
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Antifungal Metabolites (Monorden, Monocillin IV, and Cerebrosides) from Humicola fuscoatra Traaen NRRL 22980, a Mycoparasite of Aspergillus flavus Sclerotia

Donald T. Wicklow,1,* Biren K. Joshi,2 William R. Gamble,2 James B. Gloer,2 and Patrick F. Dowd1

Bioactive Agents Research, National Center for Agricultural Utilization Research, REE, Agricultural Research Service, U.S. Department of Agriculture, Peoria, Illinois 61604,1 and Department of Chemistry, University of Iowa, Iowa City, Iowa 522422

Received 18 May 1998/Accepted 3 September 1998

The mycoparasite Humicola fuscoatra NRRL 22980 was isolated from a sclerotium of Aspergillus flavus that had been buried in a cornfield near Tifton, Ga. When grown on autoclaved rice, this fungus produced the antifungal metabolites monorden, monocillin IV, and a new monorden analog. Each metabolite produced a clear zone of inhibition surrounding paper assay disks on agar plates seeded with conidia of A. flavus. Monorden was twice as inhibitory to A. flavus mycelium extension (MIC > 28 µg/ml) as monocillin IV (MIC > 56 µg/ml). Cerebrosides C and D, metabolites known to potentiate the activity of cell wall-active antibiotics, were separated from the ethyl acetate extract but were not inhibitory to A. flavus when tested as pure compounds. This is the first report of natural products from H. fuscoatra.


* Corresponding author. Mailing address: Bioactive Agents Research, REE, ARS, NCAUR, USDA, 1815 N. University St., Peoria, IL 61604. Phone: (309) 681-6243. Fax: (309) 681-6686. E-mail: wicklodt{at}mail.ncaur.usda.gov.


Applied and Environmental Microbiology, November 1998, p. 4482-4484, Vol. 64, No. 11
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Reeves, C. D., Hu, Z., Reid, R., Kealey, J. T. (2008). Genes for the Biosynthesis of the Fungal Polyketides Hypothemycin from Hypomyces subiculosus and Radicicol from Pochonia chlamydosporia. Appl. Environ. Microbiol. 74: 5121-5129 [Abstract] [Full Text]  
  • Peterson, S. W., Bayer, E. M., Wicklow, D. T. (2004). Penicillium thiersii, Penicillium angulare and Penicillium decaturense, new species isolated from wood-decay fungi in North America and their phylogenetic placement from multilocus DNA sequence analysis. Mycologia 96: 1280-1293 [Abstract] [Full Text]  
  • Bull, A. T., Ward, A. C., Goodfellow, M. (2000). Search and Discovery Strategies for Biotechnology: the Paradigm Shift. Microbiol. Mol. Biol. Rev. 64: 573-606 [Abstract] [Full Text]