Chukwuemeka R. Eke1, Peter Akomeah2and Omorefe Asemota1*
The shoot apical meristem from young suckers were used as sources of explants for initiation of culture using MS basal medium which contained 2,4-D. This was incubated at 27oC in the dark. Callogenesis was observed as early as the second subculture. Continuous subculture of the callus in the establishment medium at about the third subculture from calls production, resulted in somatic embryo formation. The somatic embryos were then transferred to MS medium without hormones under light where they matured after about two subcultures and developed into shoots. The shoots produced roots when transferred to a medium which contained NAA at 0.1 mg/L.
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