A procedure is outlined for indirect organogenesis of
Phyllanthus amarus using leaf bits and internodes.
Profuse callusing of leaf discs and internodes were obtained
on Murashige and Skoog’s basal medium supplemented with NAA
and 2,4-D. The callus thus obtained was repeatedly
sub-cultured at 3 weekly intervals for four cycles. High
frequency of callus proliferation was obtained when the
callus was sub-cultured on MS medium supplemented with BAP
(1.0 mgl-1) and glycine (50.0 mgl-1).
Complete plantlets were obtained when the callus was
sub-cultured on MS medium supplemented with BAP (2.0 mgl-1)
and GA3 (0.5 mgl-1). Rooting (87.09%)
of the shoots was best achieved on half strength MS medium
supplemented with IBA (0.5 mgl-1) and IAA (0.5
mgl-1). Regenerated plants were successfully
transferred to soil after acclimatizing them in the plant
growth chamber.