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Antimicrobial Agents and Chemotherapy, July 1998, p. 1756-1761, Vol. 42, No. 7
Institute of Biological Sciences,
Received 18 December 1997/Returned for modification 3 March
1998/Accepted 23 April 1998
The phenotype of a strain of Saccharomyces cerevisiae
containing a disruption of the gene encoding NADPH cytochrome P-450 oxidoreductase (CPR) was quantified biochemically and
microbiologically, as were those of various transformants of this
strain after expression of native CPR, cytochrome P-45051 (CYP51), and
a fusion protein of CYP51-CPR (FUS). Only a 4-fold decrease in
ergosterol biosynthesis was observed for the cpr strain,
but ketoconazole sensitivity increased 200-fold, indicating
hypersensitivity to the alternative electron donor system in
cpr strains. Both phenotypes could be reversed in
transformants expressing the CPR and FUS, indicating the
availability of the CPR in FUS as well as the expressed native CPR for
monoxygenase-associated reactions. The complementation of function was
observed both in vitro and in vivo for the monoxygenases squalene
epoxidase, CYP51, and CYP61 in the ergosterol biosynthesis pathway with
which CPR is coupled. Overexpression of CYP51 and FUS produced
different levels of ketoconazole resistance in wild-type cells,
indicating that the availability of CPR may limit the potential of
overproduction of CYP51 as a mechanism of resistance to azole antifungal agents.
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
NADPH Cytochrome P-450 Oxidoreductase and
Susceptibility to Ketoconazole
*
Corresponding author. Mailing address: Institute of
Biological Sciences, University of Wales Aberystwyth, Aberystwyth,
Ceredigion, Wales SY23 3DA, United Kingdom. Phone: 44 (1970) 622316. Fax: 44 (1970) 622350. E-mail: Steven.kelly{at}aber.ac.uk.
Antimicrobial Agents and Chemotherapy, July 1998, p. 1756-1761, Vol. 42, No. 7
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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