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Characterization of three highly purified cytochromes P-450 from hepatic microsomes of adult male rats. by D E Ryan; S Iida; A W Wood; P E Thomas; C S Lieber; W Levin is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

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Three hepatic microsomal cytochromes P-450 (P-450f, P-450g, and P-450h) have been purified to electrophoretic homogeneity from both untreated and ethanol-treated adult male rats. By all criteria examined, the hemoproteins isolated from untreated rats are indistinguishable from the corresponding enzymes purified from rats administered ethanol. Highly purified cytochromes P-450f, P-450g and P-450h are characterized by minimum Mr of 51,000, 50,000, and 51,000, respectively, and unique coordinates in two-dimensional isoelectric focusing-sodium dodecyl sulfate-polyacrylamide gels. The CO-reduced spectral maxima of cytochromes P-450f and P-450g are at 447-448 nm, and the peak of cytochrome P-450h is at 451 nm. Cytochrome P-450h is a versatile catalyst exhibiting high activity toward benzphetamine, hexobarbital, and estradiol-17 beta and moderate activity toward benzo[alpha]pyrene and zoxazolamine. In contrast, cytochromes P-450f and P-450g have low metabolic activity for these substrates. The three hemoproteins catalyze the metabolism of testosterone with different regio- and stereospecificities and overall rates. Both cytochromes P-450f and P-450h catalyze the hydroxylation of testoster

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Author

D E Ryan; S Iida; A W Wood; P E Thomas; C S Lieber; W Levin

Publisher

Elsevier BV

Published

1984

Language

EN

Field

Biochemistry, Genetics and Molecular Biology (Life Sciences)