The use of a hydrophobic resin as a product reservoir in steroid transformations.

Particles of the hydrophobic resin polydimethylsiloxane were found to preferentially accumulate steriods on the basis of their hydrophobicity. Thus, the resin selectively sorped the steroid products resulting from the transformation of diosgenin by Nocardia rhodochrous, with the result that higher yields of the later biotransformation product, 1-dehydrodiosgenone, and lower yields of the first product, diosgenone, were obtained than in the absence of resin. Furthermore, steroids accumulated by the resin were available for further biotransformation, so that a two-step reaction forming androstenes from a crude extract of furostanol glycosides (obtained from fenugreek seed) could be carried out. The first step involves deglycosylation and is catalyzed by Fusarium solani. In the presence of resin the water-insoluble diosgenin product becomes sorped to the resin and can be easily transferred to a second fermentation in which diosgenone, 1-dehydrodiosgenone, and androstenes were formed by Mycobacterium phlei. These compounds were completely accumulated by the resin at the end of the fermentation. This procedure is logistically more convenient than the conventional chemical process and illustrates the potential of biotechnological processes in which simultaneous reaction, product isolation, and product purification occur.