Immature zygotic embryos at different developmental stages were used f
or callus induction and regeneration studies. Immature embryos excised
from fruits 77, 91, 100, 114, 128, 140 and 193 days after pollination
and mature embryos were cultured on modified Y3 medium containing 500
mg l-1 cysteine, 0.5% (w/v) PVP-40, 500 muM 2.4-D and 0.3% (w/v) char
coal. Compact embryogenic tissue began differentiating directly from e
mbryo explants after 2 weeks of culture. The percentage of embryos for
ming compact embryogenic tissue ranged from 28.6% for 91-day-old embry
os to 0% for 140-day-old and older embryos. Friable embryogenic tissue
was observed in callus cultures derived from 100-day-old embryos. Alt
hough both compact and friable embryogenic tissues were successfully i
solated, normal embryo and plantlet development was observed only from
friable embryogenic tissue.