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Volume 272, Number 3,
Issue of January 17, 1997
pp. 1589-1594
©1997 by The American Society for Biochemistry and Molecular Biology, Inc.
Aspergillus nidulans stcL Encodes a Putative
Cytochrome P-450 Monooxygenase Required for Bisfuran Desaturation
during Aflatoxin/Sterigmatocystin Biosynthesis
(Received for publication, August 20, 1996, and in revised form, October 28, 1996)
Hemant S.
Kelkar
§
,
Timothy W.
Skloss
¶
,
James F.
Haw
¶
,
Nancy P.
Keller
§
and
Thomas H.
Adams
From the Departments of Biology, § Plant
Pathology, and ¶ Chemistry, Texas A&M University, College
Station, Texas 77843
The Aspergillus nidulans stcL gene is
predicted to encode a cytochrome P-450 monooxygenase and is located
within a cluster of other genes that are required for synthesis of
sterigmatocystin. Inactivation of stcL resulted in strains
that accumulate dihydrosterigmatocystin, a tetrahydrobisfuran
containing molecule that is very similar to the unsaturated product of
the wild-type pathway, sterigmatocystin. This observation led us to
hypothesize that the A. nidulans sterigmatocystin biosynthetic pathway is branched similarly to the aflatoxin pathway in
Aspergillus parasiticus and Aspergillus flavus
and that StcL is required for the desaturation of the bisfuran moiety
in the sterigmatocystin/aflatoxin precursor versicolorin B. This
prediction was confirmed by feeding the stcL mutant with
the subsequent pathway intermediate, versicolorin A, which resulted in
accumulation of both sterigmatocystin and dihydrosterigmatocystin,
indicating that StcL functions before versicolorin A synthesis.
A. nidulans stcU was shown previously to encode a
ketoreductase required to convert versicolorin A to
demethylsterigmatocystin and an stcL, stcU
double mutant strain was shown here to accumulate only versicolorin B. These results indicate that both versicolorin A and versicolorin B can
serve as substrates for StcU, resulting in a branched pathway. The
final product of each branch are sterigmatocystin and
dihydrosterigmatocystin, respectively.

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Copyright © 1997 by the American Society for Biochemistry and Molecular Biology.
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