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Applied and Environmental Microbiology, January 2000, p. 359-362, Vol. 66, No. 1
Department of Plant Pathology and
Microbiology1 and Department of
Biology,3 Texas A&M University, College
Station, Texas, and Department of Chemistry, Johns Hopkins
University, Baltimore, Maryland2
Received 8 June 1999/Accepted 2 November 1999
Sterigmatocystin (ST) and aflatoxin B1
(AFB1) are two polyketide-derived Aspergillus
mycotoxins synthesized by functionally identical sets of enzymes. ST,
the compound produced by Aspergillus nidulans, is a late
intermediate in the AFB1 pathway of A. parasiticus and A. flavus. Previous biochemical
studies predicted that five oxygenase steps are required for the
formation of ST. A 60-kb ST gene cluster in A. nidulans
contains five genes, stcB, stcF, stcL, stcS, and stcW, encoding
putative monooxygenase activities. Prior research showed that
stcL and stcS mutants accumulated versicolorins B and A, respectively. We now show that strains disrupted at
stcF, encoding a P-450 monooxygenase similar to A. parasiticus avnA, accumulate averantin. Disruption of either StcB
(a putative P-450 monooxygenase) or StcW (a putative flavin-requiring
monooxygenase) led to the accumulation of averufin as determined by
radiolabeled feeding and extraction studies.
0099-2240/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Requirement of Monooxygenase-Mediated Steps for
Sterigmatocystin Biosynthesis by Aspergillus
nidulans

and
*
Corresponding author. Mailing address: Department of
Plant Pathology and Microbiology, Texas A&M University, College
Station, TX 77843. Phone: (409) 845-0963. Fax: (409) 845-6483. E-mail: n-keller{at}tamu.edu.
Present address: Department of Genetics, University of Georgia,
Athens, GA 30602.
Present address: DeKalb Genetics, Mystic, CT 06355.
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