<span style="font-size: 21.5pt;mso-bidi-font-size:14.5pt;font-family:"Times New Roman","serif"">High frequency shoot regeneration from nodal and shoot tip explants in <i>Holarrhena antidysenterica </i><span style="font-size:21.0pt;mso-bidi-font-size: 14.0pt;font-family:"Arial","sans-serif"">L. </span></span>

Abstract

<span style="font-size: 15.5pt;mso-bidi-font-size:8.5pt;font-family:" times="" new="" roman","serif""="">Shoot tip and nodal segment explants of <i><span style="font-size:16.0pt; mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman","serif""="">Holarrhena antidysenterica </span></i><span style="font-size:15.5pt;mso-bidi-font-size: 8.5pt;font-family:" times="" new="" roman","serif""="">when cultured on MS medium containing BAP (1.0-3.0 mg/1) with NAA (0.2-1.0 mg/1) and BAP (1.0-3.0 mg/1) with Kn. (0.2-1.0 mg/1) produced multiple shoots. Maximum multiple shoots was found in MS medium supplemented with BAP (2.0 mg/1) and NAA (0.5 mg/1). Subculture on the same medium resulted in rapid shoot multiplication at an average rate of 16 new shoots per subculture. Addition of urea (100 mg/1) in the medium increased the number of shoots up to 22 per culture. For best rooting, the shoots were excised from the culture flask and implanted individually on half strength MS medium with 0.5 mg/1 each of IBA, IAA and NAA. After 20 days of transfer on root induction medium 95% rooting was achieved. Regenerated plantlets were successfully acclimatized and established in soil. About 90% of plantlets survived under open field conditions.<span style="font-size:12.5pt;mso-bidi-font-size:5.5pt;font-family:" arial","sans-serif""="">

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