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Appl. Environ. Microbiol., May 1997, 1661-1666, Vol 63, No. 5
R Prieto and CP Woloshuk
Among the enzymatic steps in the aflatoxin biosynthetic pathway, the
conversion of O-methylsterigmatocystin to aflatoxin has been proposed to be
catalyzed by an oxidoreductase. Transformants of Aspergillus flavus 649WAF2
containing a 3.3-kb genomic DNA fragment and the aflatoxin biosynthesis
regulatory gene aflR converted exogenously supplied
O-methylsterigmatocystin to aflatoxin B1. A gene, ord1, corresponding to a
transcript of about 2 kb was identified within the 3.3-kb DNA fragment. The
promoter region presented a putative AFLR binding site and a TATA sequence.
The nucleotide sequence of the gene revealed an open reading frame encoding
a protein of 528 amino acids with a deduced molecular mass of 60.2 kDa. The
gene contained six introns and seven exons. Heterologous expression of the
ord1 open reading frame under the transcriptional control of the
Saccharomyces cerevisiae galactose-inducible gal1 promoter results in the
ability to convert O-methylsterigmatocystin to aflatoxin B1. The data
indicate that ord1 is sufficient to accomplish the last step of the
aflatoxin biosynthetic pathway. A search of various databases for
similarity indicated that ord1 encodes a cytochrome P-450-type
monooxygenase, and the gene has been assigned to a new P-450 gene family
named CYP64.
Copyright © 1997, American Society for Microbiology
ord1, an oxidoreductase gene responsible for conversion of O- methylsterigmatocystin to aflatoxin in Aspergillus flavus
Department of Botany and Plant Pathology, Purdue University, West Lafayette, Indiana 47907, USA.
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