Abstract
Aspergillus fumigatus sterol 14α-demethylase isoenzymes CYP51A and CYP51B were heterologously expressed in a Saccharomyces cerevisiae mutant (YUG37-erg11), wherein native ERG11/CYP51 expression is controlled using a doxycycline-regulatable promoter. When cultured in the presence of doxycycline, recombinant YUG37-pcyp51A and YUG37-pcyp51B yeasts were able to synthesize ergosterol and grow; a control strain harboring reverse-oriented cyp51A could not. YUG37-pcyp51A and YUG37-pcyp51B constructs showed identical sensitivity to itraconazole, posaconazole, clotrimazole, and voriconazole. Conversely, YUG37-pcyp51A withstood 16-fold-higher concentrations of fluconazole than YUG37-pcyp51B (8 and 0.5 μg ml⁻¹, respectively).
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Anti-Bacterial Agents / pharmacology*
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Aspergillus fumigatus / drug effects
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Aspergillus fumigatus / enzymology*
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Azoles / pharmacology*
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Clotrimazole / pharmacology
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Cytochrome P-450 Enzyme System / genetics
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Cytochrome P-450 Enzyme System / metabolism*
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Doxycycline / pharmacology*
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Ergosterol / metabolism
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Fluconazole / pharmacology
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Fungal Proteins / genetics
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Fungal Proteins / metabolism*
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Genetic Complementation Test
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Itraconazole / pharmacology
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Pyrimidines / pharmacology
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Saccharomyces cerevisiae / genetics
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Saccharomyces cerevisiae / metabolism*
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Saccharomyces cerevisiae Proteins / genetics
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Saccharomyces cerevisiae Proteins / metabolism*
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Triazoles / pharmacology
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Voriconazole
Substances
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Anti-Bacterial Agents
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Azoles
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Fungal Proteins
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Pyrimidines
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Saccharomyces cerevisiae Proteins
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Triazoles
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Itraconazole
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posaconazole
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Fluconazole
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Cytochrome P-450 Enzyme System
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cytochrome P-450 CYP51A, Aspergillus
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cytochrome P-450 CYP51B, Aspergillus
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Erg11 protein, S cerevisiae
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Clotrimazole
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Voriconazole
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Doxycycline
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Ergosterol