A protocol was established for high frequency cyclic somatic embryogenesis
for different varieties of cassava. An efficient plant regeneration system
was developed for the high cyanogenic variety PRC 60a. Linamarin content an
d linamarase activity were determined in various tissues of secondary somat
ic embryos and regenerated plants of PRC 60a. Both linamarin and linamarase
activity were not detected in embryogenic callus, roots induced from callu
s and somatic embryo tissues. The stems and leaves of regenerated plants (i
n vitro) and storage roots and leaves of mature plants (in vivo), however,
contained variable amounts of linamarin and linamarase activity whereas in
the nonstorage root tissues (in vitro) only linamarin was detected. The pre
sent study suggested that the linamarin biosynthetic pathway may be absent
or not switched on in the embryogenic callus and somatic embryos. The ploid
y level and somatic chromosome number of the regenerated plants were found
to be same as the source plants. The availability of this regeneration syst
em would be useful not only for investigating cyanogenesis but also for gen
etic manipulation in cassava.