Callus and cell suspension cultures of Rauwolfia sellowii were established
in Gamborg B5 medium supplemented with 1 mg l(-1) 2,4-dichlorophenoxyacetic
acid, 0.2 mg l(-1) kinetin and 30 g l(-1) sucrose. The growth cycle of sus
pension cultures was completed in ca. 22 days and the maximum specific grow
th rate was 0.0098 h(-1) with a doubling time of 71 h. The cultures accumul
ated the same major alkaloids as in the leaves of the parent plant, such as
sellowiine, 19 alpha,20 alpha-epoxyakuammicine, vomilenine, picrinine and
12-demethoxytabernulosine. The alkaloid contents of leaves, callus and cell
suspension cultures were quantitatively compared by HPLC.