A novel regeneration system based on direct shoot organogenesis is des
cribed for cassava. Plants could be regenerated at high frequency by i
nducing shoot primordia on explants derived from cotyledons of cassava
somatic embryos. After a passage on elongation medium, the regenerate
d shoots were easily rooted in hormone-free medium and could be succes
sfully transplanted to soil. Using the shoot-organogenesis-based regen
eration method, up to eight transplantable plantlets per explant could
be regenerated. The system was optimised first for one cassava cultiv
ar, and then its transferability to three other cultivars was demonstr
ated. This method widens the scope of in vitro regeneration modes of c
assava, and is also compatible with Agrobacterium-mediated transformat
ion. To develop an efficient system for production of somatic embryos
for regeneration experiments. conditions for inducing primary and cycl
ing somatic embryos were also studied, and highly efficient plant rege
neration via germination of somatic embryos was achieved using maltose
instead of sucrose in the culture medium, and combining paclobutrazol
with 2,4-dichlorophenoxyacetic acid in the embryo induction medium.