Holland H L, Lakshmaiah G, Ruddock P L
Department of Chemistry, Brock University, St. Catharines, Ontario, Canada.
Steroids. 1998 Sep;63(9):484-95. doi: 10.1016/s0039-128x(98)00053-1.
An investigation of the microbial biotransformation of a range of 3 beta-, 17 beta-, and 20-acetylamino C18 to C21 steroids by microorganisms known to hydroxylate conventional steroids has been undertaken, using Aspergillus ochraceus, Bacillus megaterium, Curvularia lunata, and Rhizoputus arrhizus. A. ochraceus and B. megaterium gave products of 11 alpha- and 15 beta-hydroxylation, respectively. In the case of C. lunata, the products were predominantly those of this organism's normal C-11 beta- and C-14 alpha-hydroxylating pathways, but in one instance, 3 beta-acetylamino-7 alpha-hydroxy-5 alpha-androstan-17-one, appeared to results from direction of the site of hydroxylation by the substitution pattern of the substrate. The products from R. arrhizus generally corresponded to those previously obtained from normal steroids of similar skeleton, with 6 beta- 11 alpha-hydroxylation predominating, but again the sites of hydroxylation and the range of hydroxylated products were found to depend on the substitution pattern of the substrate.
利用已知可使传统甾体羟基化的微生物,即赭曲霉、巨大芽孢杆菌、新月弯孢霉和无根根霉,对一系列3β-、17β-和20-乙酰氨基C18至C21甾体的微生物生物转化进行了研究。赭曲霉和巨大芽孢杆菌分别产生了11α-和15β-羟基化产物。对于新月弯孢霉,产物主要是该生物体正常的C-11β-和C-14α-羟基化途径的产物,但在一个实例中,3β-乙酰氨基-7α-羟基-5α-雄甾烷-17-酮似乎是由底物的取代模式引导羟基化位点而产生的。无根根霉的产物通常与先前从具有相似骨架的正常甾体中获得的产物相对应,以6β-11α-羟基化为主,但同样发现羟基化位点和羟基化产物的范围取决于底物的取代模式。