In this research study in vitro regeneration protocols were established for Colocasia esculenta L. Schott (stoloniferous) using stolon bud explant. MS supplemented with different concentration and combinations of auxins and cytokinins were used for the induction of direct and indirect organogenesis and rootings. 91 % culture responded to shoot proliferation using stolon bud explants on MS having 6.0 mg L ‐1BAP +1.0 mg L‐1 NAA. Direct multiple shoot regeneration (83%) was also observed on MS supplementing 6.0 mg L ‐1BAP +1.0 mg L‐1 NAA. In vitro derived petiole callus induction (65 %) was found in C. esculenta L. Schott on MS media containing 1.0 mg L –1 BAP + 2.0 mg L‐1 2, 4‐D. In vitro derived callus regeneration (60 %) was observed in media having 1.0 mg L ‐1BAP + 1.5 mg L‐1NAA in C. escuelnta (stoloniferous). Profuse root development was found MS having 0.5 mg L‐1IAA. Regenerated plantlets were acclimatized with all agronomic practices in the plastic pots for normal growth and development in successfully.
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