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The aim of this study was to establish an effective method of micropropagation of globe artichoke from shoot-hp. This study involved establishment of an aseptic culture. multiplication of proliferated shook, rooting of these shook in vitro and adaptation of plantlets for free living Highest survival percentage with no contamination was achieved after sterilizing the explants with 70% ethanol (5 Sec.) + 1.5 % sodium hypochlorite for 20 min. The bast results of preventing browning of explants were obtained with 100 mg/1 ascorbic acid. The highest proliferated shook were obtained when shoot tip with 4 mm length (taken in mid March) were cultured on MS medium with 10mg/1 Kin. + 0.5 mg/l IAA. The highest multiplication rate was obtained when recultured on MS medium supplemented with 5 mg/1 Kin. + 0.5 mg/1 IAA. Multiplication rate gradually increased with increasing number of subculturing till Me third subculture but subsequent subculture (4 th  subculture) had a low rate.

901 PB 538 STUDIES ON PROPAGATION OF GLOBE ARTICHOKE THROUGH TISSUE CULTURE TECHNIQUE