verrucossa [16], C. halicacabum [5], Rubia

cordifolia [19], and Tecomella undulata [20]. Several researches have demonstrated that TDZ unlike traditional cytokinins is capable of fulfilling both cytokinin and auxin requirements of various PFT�� solubility dmso regenerative responses in many different plant species. Such studies are supported by the fact that there may be a possibility of high natural endogenous cytokinin content within the plant species. This explanation further finds supports by the fact that adventitious root growth often appears spontaneously on plant stems of many cultivars [21]. It is likely that TDZ results in a balanced ratio of endogenous growth regulators that allows for specific mode of regeneration to take place and this is likely to be dependent on the level of TDZ provided in the medium

and species. Hare and Van Staden [22] also reported that TDZ has a capacity to inhibit (atleast partially) the action of cytokinin oxidase, which in turn may increase the level of endogenous cytokinins. When compared to purine based cytokinin i.e., BA, TDZ is found to be active at lower concentrations. Here, BA gave optimum response on 5.0 μM (Table 1). The aminopurine cyotkinins have similar effects at higher concentrations i.e., in between 1 μM and 10 μM. This range with TDZ results in excessive callus formation and cessation of shoot growth.

The TDZ alone is more effective than adenine-based compounds for inducing axillary shoot formation in many woody species Talazoparib in vivo [15]. But Palla and Pijut [23] reported adventitious regeneration from hypocotyls Carteolol HCl of Fraxinus only in combination with BA. However, an over- abundance of TDZ has been shown to have negative effects in vitro, such as inhibition of shoot elongation, tight bud clusters with some leaf expansion and hyperhydricity that could be a factor limiting further adventitious shoot formation. Inhibition of shoot elongation may be due to high cytokinin activity of TDZ, whereas the presence of phenyl group may be a possible cause of shoot bud fasciation [15]. Similar pattern of deformities have been reported in several plants including Daphne sp. [24], Ziziphus jujuba [25], and R. cordifolia [19]. To overcome deleterious effect of continued presence of TDZ on growth and multiplication of shoots, these shoots were transferred to a secondary medium lacking TDZ (growth regulator free MS media). The procedure applied here substantiates and has been successfully applied in a number of plant species viz., Morus alba [26], Cassia angustifolia [27], C. halicacabum [5], Cotoneaster wilsonii [28] and N. arbor-tristis [18]. The effect of subculture passage was also evaluated on shoot cultures induced from TDZ.