Abstract
An efficient regeneration protocol for Sarcostemma acidum - an important medicinal plant has been established. Callus initiated from nodal explant on MS medium with 2.0 mg L(-1) of NAA + additives. Callus initiated was subcultured on MS medium containing various concentrations of NAA or 2,4-D. Out of these combinations, MS medium +1.0 mg L(-1) of NAA + additives was found to be effective for the multiplication of callus. Subculture was done after an interval of 20-22 days. For differentiation of callus BAP or Kinetin alone was found to be less effective. Maximum frequency of shoot regeneration recorded on MS medium +1.0 mg L(-1) of BAP + 0.5 mg L(-1) of Kinetin and 0.1 mg L(-1) of NAA + additives. The in vitro differentiated shoots were excised and inoculated on 1/4 strength MS medium +2.0 mg L(-1) of IBA + 0.02 % activated charcoal for in vitro rooting. Maximum response (90 %) was recorded on this medium. In vitro differentiated shoots were inoculated on autoclaved soilrite® after treatment with root inducing auxins. Ex vitro rooting in this plant species has been reported for the first time. Eighty five percent of the shoots rooted under ex vitro conditions. Both in vitro and ex vitro rooted plantlets were hardened in a green house.