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*Corresponding author, E-mail: tiwarig_111@yahoo.co.in.
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A protocol has been established to propagate local cultivar of Glycyrrhiza glabra (L.) through indirect and direct in vitro organogenesis from nodal segment explants excised from 4–5 months-old plants. In the present study, induction medium B52D (B5 + 2.0 mgl−1 2, 4 D + 20.0 gl−1 sucrose + 7.5 gl−1 agar) induced callusing in higher frequencies (65.93%). Culture medium B5.5B.5N (B5 + 0.5 mgl−1 BA + 0.5 mgl−1 NAA + 20.0 gl−1 sucrose + 7.5 gl−1 agar) was found to be more responsive for shoot proliferation (94.12%), shoots per explant (9.32) and mean shoot length (5.20 cm). Among rooting media B5.5I (B5 + 0.5 mgl−1 IBA+ 10.0 gl−1 sucrose + 7.5 gl−1 agar) proved to be superior for higher root proliferation (84.92%) and mean root length (2.13 cm). Regenerated plantlets were established successfully in the field after hardening.
Glycyrrhiza glabra, nodal segment culture, organogenesis, plantlet regeneration