2007•Plant BiotechnologyOpen access

Micropropagation and in vitro flowering in Pentanema indicum Ling

Iyyakkannu Sivanesan, Byoung Ryong Jeong

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Abstract

In this study we have investigated micropropagation and in vitro flowering for a medicinally important plant Pentanema indicum. Maximum callus proliferation was obtained on MS medium supplemented with 2.0 mg l−1 BAP and 1.0 mg l−1 IBA. The best shoot regeneration (19±1.0) was achieved in five weeks when callus was cultured on MS medium amended with 4.0 mg l−1 BAP and 1.0 mg l−1 IAA. Direct multiple shoot initiation was also obtained from shoot tip and nodal explants in the presence of BAP and IAA. Addition of adenine sulfate (1.0 mg l−1) to the regeneration medium increased the shoot multiplication. Regenerated shoots rooted best on MS medium containing 2.0 mg l−1 IBA. Multiple shoots regenerated from callus, shoot tip and nodal explants flowered (90%) in vitro on a MS medium fortified with 2.0 mg l−1 IBA. Plantlets were successfully acclimatized in a soil condition and the survival rate was 96%.

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In this study we have investigated micropropagation and in vitro flowering for a medicinally important plant Pentanema indicum. Maximum callus proliferation was obtained on MS medium supplemented with 2.0 mg l−1 BAP and 1.0 mg l−1 IBA. The best shoot regeneration (19±1.0) was achieved in five weeks when callus was cultured on MS medium amended with 4.0 mg l−1 BAP and 1.0 mg l−1 IAA. Direct multiple shoot initiation was also obtained from shoot tip and nodal explants in the presence of BAP and IAA. Addition of adenine sulfate (1.0 mg l−1) to the regeneration medium increased the shoot multiplication. Regenerated shoots rooted best on MS medium containing 2.0 mg l−1 IBA. Multiple shoots regenerated from callus, shoot tip and nodal explants flowered (90%) in vitro on a MS medium fortified with 2.0 mg l−1 IBA. Plantlets were successfully acclimatized in a soil condition and the survival rate was 96%.

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Available abstract

In this study we have investigated micropropagation and in vitro flowering for a medicinally important plant Pentanema indicum. Maximum callus proliferation was obtained on MS medium supplemented with 2.0 mg l−1 BAP and 1.0 mg l−1 IBA. The best shoot regeneration (19±1.0) was achieved in five weeks when callus was cultured on MS medium amended with 4.0 mg l−1 BAP and 1.0 mg l−1 IAA. Direct multiple shoot initiation was also obtained from shoot tip and nodal explants in the presence of BAP and IAA. Addition of adenine sulfate (1.0 mg l−1) to the regeneration medium increased the shoot multiplication. Regenerated shoots rooted best on MS medium containing 2.0 mg l−1 IBA. Multiple shoots regenerated from callus, shoot tip and nodal explants flowered (90%) in vitro on a MS medium fortified with 2.0 mg l−1 IBA. Plantlets were successfully acclimatized in a soil condition and the survival rate was 96%.

Key concepts: Shoot, Explant culture, Callus, Micropropagation, Biology, Murashige and Skoog medium, Botany, In vitro

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