Item Type: | Article |
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Title: | The mechanism of the acyl-carbon bond cleavage reaction catalyzed by recombinant sterol 14 alpha-demethylase of Candida albicans (other names are: lanosterol 14 alpha-demethylase, P-45014DM, and CYP51) |
Creators Name: | Shyadehi, A.Z., Lamb, D.C., Kelly, S.L., Kelly, D.E., Schunck, W.H., Wright, J.N., Corina, D. and Akhtar, M. |
Abstract: | The Candida albicans sterol 14 alpha-demethylase gene (P-45014DM, CYP51) was transferred to the yeast plasmid YEp51 placing it under the control of the GAL10 promoter. The resulting construct (YEp51:CYP51) when transformed into the yeast strain GRF18 gave a clone producing 1.5 mu mol of P-450/liter of culture, the microsomal fraction of which contained up to 2.5 nmol of P-450/mg of protein. Two oxygenated precursors for the 14 alpha-demethylase, 3 beta-hydroxylanost-7-en-32-al and 3 beta-hydroxylanost-7-en-32-ol, variously labeled with 2H and 18O at C-32 were synthesized. In this study the conversion of [32-2H,32-16O]- and [32-2H,32-18O]3 beta-hydroxylanost-7-en-32-al with the recombinant 14 alpha-demethylase was performed under 16O2 or 18O2 and the released formic acid analyzed by mass spectrometry. The results showed that in the acyl-carbon bond cleavage step (i.e. the deformylation process) the original carbonyl oxygen at C-32 of the precursor is retained in formic acid and the second oxygen of formate is derived from molecular oxygen; precisely the same scenario that has previously been observed for the acyl-carbon cleavage steps catalyzed by aromatase (P-450arom) and 17 alpha-hydroxylase-17,20-lyase (P-45017 alpha,CYP17). In the light of these results the mechanism of the acyl-carbon bond cleavage step catalyzed by the 14 alpha-demethylase is considered. |
Keywords: | Base Sequence, Candida Albicans, Catalysis, Cytochrome P-450 Enzyme System, DNA Primers, Mass Spectrometry, Microsomes, Molecular Sequence Data, Oxidoreductases, Oxygen, Recombinant Proteins, Sterol 14-Demethylase |
Source: | Journal of Biological Chemistry |
ISSN: | 0021-9258 |
Publisher: | American Society for Biochemistry and Molecular Biology |
Volume: | 271 |
Number: | 21 |
Page Range: | 12445-12450 |
Date: | 24 May 1996 |
Official Publication: | https://doi.org/10.1074/jbc.271.21.12445 |
PubMed: | View item in PubMed |
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