Wiebe J P, Larner J M
Steroids. 1977 Nov;30(5):691-702. doi: 10.1016/0039-128x(77)90058-7.
A simple procedure is described for solubilizing microsomal 3beta-hydroxysteroid dehydrogenase (3beta-HSD). Microsomes from rat adrenals or from testicular interstitial cells were incubated for 1 or 2 h at 0 C in a buffer containing NaCl followed by overnight storage at -20 C. Maximum solubilization of 3beta-hydroxy-5beta-androstan-17-one-HSD (androstane-3beta-HSD) was obtained by incubating adrenal microsomes with 1 M NaCl and interstitial cell microsomes with 2 M NaCl. Incubation with NaCl for 1 or 2 h resulted in maximum solubilization; incubation with NaCl for 4, 8 or 24 h did not change the amount of enzyme solubilized. From adrenal microsomes incubated with 1 M NaCl, up to 80% (105.7 millimicron/mg microsomes) of the total androstane-3beta-HSD activity was recovered in the supernatant following centrifugation at 130,000 x g for 1 h. The maximum amount of androstane-3beta-HSD solubilized from interstitial cell microsomes was 56% (29.5 millimicron/mg microsomes) at 2 M NaCl. The "solubilized" androstane-3beta-HSD was retarded when chromatographed on a Sephadex G-200 column and it did not pellet out when centrifuged at 130,000 x g for 15 h. KCL appeared to be equally effective in solubilizing androstane-3beta-HSD from microsomes. Other steroid dehydrogenase activities such as pregnanolone-HSD and 3beta-hydroxy-5alpha-androstan-17-one-HSD were also found in the 130,000 x g supernatant.
本文描述了一种用于溶解微粒体3β-羟基类固醇脱氢酶(3β-HSD)的简单方法。将大鼠肾上腺或睾丸间质细胞的微粒体在含氯化钠的缓冲液中于0℃孵育1或2小时,然后在-20℃过夜保存。通过将肾上腺微粒体与1M氯化钠孵育以及将间质细胞微粒体与2M氯化钠孵育,可实现3β-羟基-5β-雄甾烷-17-酮-HSD(雄甾烷-3β-HSD)的最大溶解。用氯化钠孵育1或2小时可实现最大溶解;用氯化钠孵育4、8或24小时不会改变溶解的酶量。从用1M氯化钠孵育的肾上腺微粒体中,在130,000×g离心1小时后,上清液中可回收高达80%(105.7毫微摩尔/毫克微粒体)的总雄甾烷-3β-HSD活性。在2M氯化钠条件下,从间质细胞微粒体中溶解的雄甾烷-3β-HSD的最大量为56%(29.5毫微摩尔/毫克微粒体)。“溶解的”雄甾烷-3β-HSD在Sephadex G-200柱上进行色谱分析时迁移缓慢,在130,000×g离心15小时时不会沉淀。氯化钾在从微粒体中溶解雄甾烷-3β-HSD方面似乎同样有效。在130,000×g的上清液中还发现了其他类固醇脱氢酶活性,如孕烷醇酮-HSD和3β-羟基-5α-雄甾烷-17-酮-HSD。