| Literature DB >> 33189850 |
Sarah M Glass1, Michael J Reddish2, Stella A Child1, Clayton J Wilkey1, Donald F Stec3, F Peter Guengerich4.
Abstract
Cytochrome P450 (P450) 11B1 and 11B2 both catalyze the 11β-hydroxylation of 11-deoxycorticosterone and the subsequent 18-hydroxylation of the product. P450 11B2, but not P450 11B1, catalyzes a further C-18 oxidation to yield aldosterone. 11-Oxygenated androgens are of interest, and 11-hydroxy progesterone has been reported to be a precursor of these. Oxidation of progesterone by purified recombinant P450 11B2 yielded a mono-hydroxy derivative as the major product, and co-chromatography with commercial standards and 2-D NMR spectroscopy indicated 11β-hydroxylation. 18-Hydroxyprogesterone and a dihydroxyprogesterone were also formed. Similarly, oxidation of androstenedione by P450 11B2 yielded 11β-hydroxyandrostenedione, 18-hydroxyandrostenedione, and a dihydroxyandrostenedione. The steady-state kinetic parameters for androstenedione and progesterone 11β-hydroxylation were similar to those reported for the classic substrate 11-deoxycorticosterone. The source of 11α-hydroxyprogesterone in humans remains unresolved.Entities:
Keywords: 11 β-Hydroxyandrostenedione; 11-Hydroxy steroids; 11β-Hydroxyprogesterone; 18-Hydroxy steroids; Androstenedione; Cytochrome P450 11B2; Progesterone
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Year: 2020 PMID: 33189850 PMCID: PMC7954869 DOI: 10.1016/j.jsbmb.2020.105787
Source DB: PubMed Journal: J Steroid Biochem Mol Biol ISSN: 0960-0760 Impact factor: 4.292