A study was carried out at the Biotechnology-cum-Tissue Culture Centre, OUAT, Bhubaneswar, India, to standardise the surface sterilization time and media supplements for culture establishment and better proliferation and media supplements for root formation of a wonderful landscape shrub B.galpinii which is difficult to propagate. For in vitro studies, single node explants (6-8mm size) were taken from branches of Bauhinia galpinii plants. The explants were surface sterilized with 0.1% HgCl2 for different time periods i.e. 2 minutes, 4 minutes, 6 minutes, 8 minutes, 10minutes, 12minutes and 15minutes under the laminar air flow cabinet, followed by a dip in 1% KCI for 1 minute. For surface sterilization study, the explants were cultured on MS medium supplemented with 1.0mg/l Kinetin along with 0.5mg/l NAA for initial culture establishment for 30 days and observations were recorded on various sterilization characters. For shoot proliferation study, the explants were surface sterilized with the best treatment and cultured on MS medium alone or in combination with NAA (0.5 and 1.0mg/ l) and IAA (0.1 and 0.2mg/l) for 30 days. Then, 4.5-6.5 cm shoots were cultured on MS medium alone or in combination with NAA (0.5, 1.0, 1.5, and 2.0mg/l) and IAA (0.25, 0.5, 1.0, and 1.5mg/l) for root formation study for 30 days. The results revealed that 0.1% HgC12 for 6 minutes was most effective for sterilization of the single node explants of B. galpinii , where the treatment recorded no contamination and death, higher percentage of aseptic culture (100.0%) and survival (100.0%), early bud initiation (11.10 days) , production of more number of shoots / explants (2.07) and longer shoot(5.37 cm) . MS medium fortified with Kinetin 1.0mg/l and IAA 0.1mg/1 (3.30) was the best combination for early shoot initiation(8.67 days), production of maximum number of shoots / explant (2.00), longer shoot (8.00 cm) , more number of branches / shoot (1.97) and leaves per shoot mass(8.10) of light green colour . A branch containing 10 nodes can produce 20 shoots in in vitro condition which is not possible in in vivo condition. Within a period of 30 days, none of the explants developed root primordial, hence further studies on this aspect are essential.
Bauhinia galpinii, explants, invitro.
Babu, K.N., R. Samsudeen and M.J. Ratnammal (1992). In vitro plant regeneration from
leaf-derived callus in ginger (Zingiber officinale Rosc.). Plant Cell. Tissue and Organ Cult. 29:71-74.
Berardi, G. (1989). Preliminary studies on the in vitro regeneration of plantlets from rose petals. Colture Protett, 18(8-9):111-113.
Beura, S. (1998). In vitro multiplication, agro-bacterium mediated transformation and post- harvest handling of spikes in Gladiolus.Ph.D. thesis. GBPUAT, Pantnagar, 220p.
Bhaskar, J. (1991). Standardization of in vitro propagation technique in banana. M.Sc. (Hort.) thesis submitted to Kerala Agriculture University. Vellanikkara, Kerala.
Bhatia, R., K.P. Singh and M.C. Singh (2008) .Effect of growth regulators on regeneration from leaf-derived callus and shoot proliferation in gerbera. Indian J Hort., 65:312–316.
Debergh, P.C. and L.J. Maene (1981). A scheme for commercial propagation of ornamental plants by tissue culture, Sci. Hort. 14:335-345.
Gomez K.A. and A.A. Gomez (1984). Statistical Procedures for Agriculture Research (2nd edn.) John Willey and Sons, Inc., New York.68 p.
Hsia, C. N. and S.S. Korban (1996). Organogenesis and somatic embryo-genesis in callus cultures of Rosa hybrida and Rosa chinensis minima. Plant Cell Tissue and Organ Culture. 44:(1)1-6.
Hussey, G. (1975). Totipotency in tissue explants and callus of some members of Liliaceae, Iridaceae and Amaryllidaceae. J. Exp. Bot. 26(91): 253-262.
Hussey, G. (1976). In vitro release of axillary shoots from apical dominance in monocotyled onous plantlets. Ann. Bot., 40:1323-25.
Kobza, F. and J. Vachunova (1991). Propagation of Dracaena in vitro II. Propagation of
Dracaena concinna Kunth. Acta universitatitis- Agriculturae, Facultas Hort. 6:51- 55.
Kobza, F. and J. Vachunova .(1989). Propagation of Dracaena: In vitro propagation of Dracaena deremensis Engl. Acta Universititis- Agriculturae, Facultas- Horticultarae. 4(2):33-37.
Moore, T.C. (1989). Cytokinin In: Biochemistry and Physiology of Plant Hormones, Narosa Publishing House, New Delhi. 159-195.
Murasighe, T. (1974). Plant propagation through tissue culture. Ann. Rev. Pl. Physiol. 25:135-166.
Murasighe, T. and F. Skoog (1962). A revised medium for rapid growth and bioassays with tobacco tissue culture. Physicologia Plantarum, 15: 473-497.
Shailja, P. V., S. S. Patil and M. K. Kumari (2004). Rapid clonal multiplication of Gerbera jamesonii through tissue culture. Journal of Ornamental Horticulture. 7(3-4): 283-287.
Syamal, M.M. and S.K. Singh (1994). Micro propagation in Rose cv. Sonia. Journal of Ornamental Horticulture. 2:(1-2) 37-41.
Wilson, D. and N.K. Nayar (1998). In vitro propagation of Rose CV. Folklore Journal of Tropical Agriculture. 36(1-2) 12-17.