Characterization of the Aspergillus nidulans Monodictyphenone Gene Cluster

Author:

Chiang Yi-Ming12,Szewczyk Edyta3,Davidson Ashley D.3,Entwistle Ruth4,Keller Nancy P.56,Wang Clay C. C.27,Oakley Berl R.34

Affiliation:

1. Graduate Institute of Pharmaceutical Science, Chia Nan University of Pharmacy and Science, Tainan 71710, Taiwan, Republic of China

2. Department of Pharmacology and Pharmaceutical Sciences, University of Southern California, School of Pharmacy, 1985 Zonal Avenue, Los Angeles, California 90089

3. Department of Molecular Genetics, Ohio State University, 484 West 12th Avenue, Columbus, Ohio 43210

4. Department of Molecular Biosciences, University of Kansas, 1200 Sunnyside Avenue, Lawrence, Kansas 66045

5. Department of Medical Microbiology and Immunology, University of Wisconsin—Madison, Madison, Wisconsin 53706

6. Department of Bacteriology, University of Wisconsin—Madison, Madison, Wisconsin 53706

7. Department of Chemistry, University of Southern California, College of Letters, Arts, and Sciences, Los Angeles, California 90089

Abstract

ABSTRACT Deletion of cclA , a component of the COMPASS complex of Aspergillus nidulans , results in the production of monodictyphenone and emodin derivatives. Through a set of targeted deletions in a cclA deletion strain, we have identified the genes required for monodictyphenone and emodin analog biosynthesis. Identification of an intermediate, endocrocin, from an mdpH Δ strain suggests that mdpH might encode a decarboxylase. Furthermore, by replacing the promoter of mdpA (a putative aflJ homolog) and mdpE (a putative aflR homolog) with the inducible alcA promoter, we have confirmed that MdpA functions as a coactivator. We propose a biosynthetic pathway for monodictyphenone and emodin derivatives based on bioinformatic analysis and characterization of biosynthetic intermediates.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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