Three clones of enset (Ensete ventricosum Welw. Cheesman) from southwestern
Ethiopia (Keffa-Shaka zone) were investigated for their potential for micr
opropagation and regeneration in tissue culture. Corm and leaf tissue of gr
eenhouse-grown plants as well as in vitro germinated zygotic embryos were u
sed as starting material for micro-propagation and regeneration studies. Em
bryos were excised from disinfected seeds and cultured in vitro. Multiple s
hoots from both corm- and embryo-explants were obtained using regeneration
medium supplemented with 10 muM or 20 muM BAP. Rooting of shoots was achiev
ed using medium with 5 muM IBA, 1 muM BAP and 1 g l(-1) activated charcoal.
Plantlets obtained by this process were transferred to soil under greenhou
se conditions. Optimal conditions, which were determined for clonal propaga
tion of three different genotypes of enset, allowing both in vitro micropro
pagation and regeneration, are described. This protocol makes for conservat
ion of enset clones, rapid propagation of selected disease-free germplasm a
nd more efficient breeding procedures.