Cryptic Aspergillus nidulans Antimicrobials

Author:

Giles Steve S.1,Soukup Alexandra A.2,Lauer Carrie1,Shaaban Mona13,Lin Alexander4,Oakley Berl R.5,Wang Clay C. C.46,Keller Nancy P.17

Affiliation:

1. Department of Medical Microbiology and Immunology, University of Wisconsin—Madison, Madison, Wisconsin

2. Department of Genetics, University of Wisconsin—Madison, Madison, Wisconsin

3. Microbiology and Immunology, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt

4. Department of Pharmacology and Pharmaceutical Sciences, University of Southern California, 1985 Zonal Avenue, Los Angeles, California 90033

5. Department of Molecular Biosciences, University of Kansas, Lawrence, Kansas

6. Department of Chemistry, University of Southern California, 1985 Zonal Avenue, Los Angeles, California 90033

7. Department of Bacteriology, University of Wisconsin—Madison, Madison, Wisconsin

Abstract

ABSTRACT Secondary metabolite (SM) production by fungi is hypothesized to provide some fitness attribute for the producing organisms. However, most SM clusters are “silent” when fungi are grown in traditional laboratory settings, and it is difficult to ascertain any function or activity of these SM cluster products. Recently, the creation of a chromatin remodeling mutant in Aspergillus nidulans induced activation of several cryptic SM gene clusters. Systematic testing of nine purified metabolites from this mutant identified an emodin derivate with efficacy against both human fungal pathogens (inhibiting both spore germination and hyphal growth) and several bacteria. The ability of catalase to diminish this antimicrobial activity implicates reactive oxygen species generation, specifically, the generation of hydrogen peroxide, as the mechanism of emodin hydroxyl activity.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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