Blais C, Dauphin-Villemant C, Kovganko N, Girault J P, Descoins C, Lafont R
Ecole Normale Supérieure, Laboratoire de Biochimie, CNRS EP 119, Paris, France.
Biochem J. 1996 Dec 1;320 ( Pt 2)(Pt 2):413-9. doi: 10.1042/bj3200413.
Although the involvement of 3-oxo-delta 4 compounds as intermediates in arthropod ecdysteroid biosynthesis has been postulated for a long time, it has not yet been directly demonstrated. In the present study, 3-oxo-delta 4-steroids have been synthesized and incubated in vitro with dissociated moulting gland cells from the crab Carcinus maenas. The tritiated compounds were converted into 3-dehydroecdysone, ecdysone and/or 25-deoxyecdysone, i.e. final ecdysteroids. This means that the 3-oxo-delta 4 compounds had undergone a 5 beta-reduction, to give the 5 beta-conformation of ecdysteroids. Our results suggest that the 3-oxo-delta 4-steroid 4,7-cholestadien-14 alpha-ol-3,6-dione may be an intermediate in the biosynthetic pathway. The 5 beta-reduction reaction involves a cytosolic enzyme which requires NADPH as electron donor and seems specific for 3-oxo-delta 4 substrates. This reaction was the most active in crab Y-organs, as compared with other tissues. The characteristics of the 5 beta-reductase (subcellular localization, substrate and cofactor requirements) appear similar to those of the vertebrate 3-oxo-delta 4-steroid 5 beta-reductase involved in steroid hormone catabolism and bile acid biosynthesis.
尽管3-氧代-δ4化合物作为节肢动物蜕皮甾体生物合成中间体的参与作用已被推测了很长时间,但尚未得到直接证实。在本研究中,已合成3-氧代-δ4-甾体,并在体外与来自普通黄道蟹的解离蜕皮腺细胞一起孵育。氚标记的化合物被转化为3-脱氢蜕皮激素、蜕皮激素和/或25-脱氧蜕皮激素,即最终的蜕皮甾体。这意味着3-氧代-δ4化合物经历了5β-还原,形成了蜕皮甾体的5β-构象。我们的结果表明,3-氧代-δ4-甾体4,7-胆甾二烯-14α-醇-3,6-二酮可能是生物合成途径中的一种中间体。5β-还原反应涉及一种胞质酶,该酶需要NADPH作为电子供体,并且似乎对3-氧代-δ4底物具有特异性。与其他组织相比,该反应在蟹Y器官中最为活跃。5β-还原酶的特性(亚细胞定位、底物和辅因子需求)似乎与参与甾体激素分解代谢和胆汁酸生物合成的脊椎动物3-氧代-δ4-甾体5β-还原酶相似。