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Abstract

A protocol was developed for callus induction and regeneration in tomato (Lycopersicon esculentum) var. Moneymaker. Hypocotyl and leaf disc explants of tomato were used as a starting material for callus induction. Explants were cultured on MS medium having different concentrations of hormones. Maximum callogenesis from hypocotyls was obtained on MS medium supplemented with IAA (2 mg/l), NAA (2 mg/l), BAP (5 mg/l) and Kin (4 mg/l). It was 65.2% for hypocotyls. For leaf discs maximum callogenesis was achieved on MS medium supplemented with IAA (2 mg/l), NAA (2 mg/l), BAP (2 mg/l) and Kin (4 mg/l). It was 81.3% for leaf discs. Calli were cultured on MS medium having concentrations of Zeatin (1 mg/l) and IAA (1 mg/l) for regeneration. They showed maximum regeneration of 69.2% from hypocotyls. Minimum regeneration of 2.8% was obtained on MS medium supplemented with IAA (2 mg/l), NAA (2 mg/l), BAP (2 mg/l) and Kin (4 mg/l). Tomato shoots were shifted to ½ MS medium containing IBA (0.1 mg/l) and BAP (0.0025 mg/l) for rooting and all responded positively to rooting.

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