Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, 37232-0146, United States.
Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, 37232-0146, United States; Department of Chemistry and Fermentation Sciences, Appalachian State University, Boone, NC, 28608, United States.
J Steroid Biochem Mol Biol. 2021 Apr;208:105787. doi: 10.1016/j.jsbmb.2020.105787. Epub 2020 Nov 12.
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.
细胞色素 P450(P450)11B1 和 11B2 均催化 11-脱氧皮质酮的 11β-羟化作用以及产物的随后 18-羟化作用。P450 11B2 但不是 P450 11B1 催化进一步的 C-18 氧化以生成醛固酮。11-氧代雄激素很重要,据报道 11-羟基孕酮是这些物质的前体。通过纯化的重组 P450 11B2 氧化孕酮生成单羟基衍生物作为主要产物,与商业标准和 2-D NMR 光谱的共色谱分析表明存在 11β-羟化作用。18-羟基孕酮和二羟基孕酮也形成。同样,P450 11B2 氧化雄烯二酮生成 11β-羟基雄烯二酮、18-羟基雄烯二酮和二羟基雄烯二酮。雄烯二酮和孕酮 11β-羟化的稳态动力学参数与经典底物 11-脱氧皮质酮报道的参数相似。人体内 11α-羟基孕酮的来源仍未解决。