210-214An efficient in vitro propagation
system was established for direct shoot regeneration in Clitoria ternatea L.. The
regeneration protocol was standardized by using different explants, viz., nodal,
cotyledonary node and shoot tip, on Murashige and Skoog (MS) medium with
different concentrations of sucrose (1-6% ), plant growth regulators BA and Kn
(1.0-6.0 µM), and
different levels of pH (5.2-6.2). The highest mean number of shoots (18.7±1.0) was
obtained from nodal explants on MS medium containing 3% sucrose and 0.8% agar
supplemented with BA (5.0 µM) at pH 5.8. In vitro regenerated and elongated shoots were rooted on ½ MS
medium fortified with IBA (2.0 µM). Complete plantlets
were then hardened, acclimatized and transplanted to natural conditions, where
they exhibited 80% survivability