Transformation of jervine by Cunninghamella elegans ATCC 9245

Preparative-scale fermentation of the known C-nor-D-homosteroidal jerveratr um alkaloid jervine with Cunninghamella elegans (ATCC 9245) has resulted in the isolation of (-)-jervinone as the major metabolite. In addition, C. el egans ATCC 9245 was able to epimerize C-3 of jervine, producing 3-epi-jervi ne. This epimerization reaction was similar to that reported for tomatidine , the known spirosolane-type Solanum alkaloid. The structure elucidation of both metabolites was based primarily on 1D- and 2D-NMR analyses. (C) 2000 Elsevier Science Ltd. All rights reserved.