Kwan T K, Taylor N F, Watson D, Gower D B
FEBS Lett. 1984 Aug 20;174(1):173-8. doi: 10.1016/0014-5793(84)81099-6.
The biosynthesis of 16-androstenes has been studied in neonatal porcine testicular microsomes using 17-hydroxypregnenolone and 16-dehydropregnenolone, separately, as substrates. The metabolites formed after microsomal incubation with these substrates were purified, derivatized as O-methyloxime-trimethylsilyl ethers and analysed by capillary gas chromatography-mass spectrometry. In the incubation of 17-hydroxypregnenolone with microsomes, 16-dehydropregnenolone was identified as an intermediate in the biosynthesis of 16-androstenes. Further microsomal incubation of 16-dehydropregnenolone has established the intermediary role of this steroid in the production of 16-androstenes.
利用17-羟孕烯醇酮和16-脱氢孕烯醇酮分别作为底物,对新生猪睾丸微粒体中16-雄烯类化合物的生物合成进行了研究。将这些底物与微粒体孵育后形成的代谢产物进行纯化,衍生化为O-甲基肟-三甲基硅醚,并通过毛细管气相色谱-质谱联用仪进行分析。在17-羟孕烯醇酮与微粒体的孵育过程中,16-脱氢孕烯醇酮被鉴定为16-雄烯类化合物生物合成的中间体。对16-脱氢孕烯醇酮进行进一步的微粒体孵育,证实了该类固醇在16-雄烯类化合物生成中的中间作用。