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Seema S<strong>in</strong>gh et al., IJSID 2011, 1 (2), 247-254and full strength media, supplemented with IBA (0.1mg/L) and NAA (1.0 mg/L), produced roots andconsequently the plantlets could be developed.CONCLUSIONIt is apparent from these results that MS media supplemented with BAP(1mg/L)+ Kn(1mg/L)+IAA(1mg/L) is more efficient <strong>for</strong> multiple <strong>shoot</strong> <strong>regeneration</strong> and it may be utilized <strong>in</strong> <strong>in</strong>-vitroimprovement program of Brassica campestris(L.) var. sawarna because <strong>in</strong> Brassica species organogenesisresponse are species and genotype specific 13 .REFERENCES1. Ali H, Ali Z, Ali HA, Mehmood S, Ali W (2007). In-vitro <strong>regeneration</strong> of Brassica napus L., cultivars (Star, Cyclone andWestar) from hypocotyls and cotyledonary leaves. Pakistan Journal of Botany 39(4), 1251-1256.2. Glemelius K., 1984. High growth rate and <strong>regeneration</strong> capacity of hypocotyl protoplast <strong>in</strong> some Brassicaceae, PhysiologyPlant 61:38-44.3. Lazzeri, P.A., Dunwell J.M., 1984 a. In-vitro <strong>shoot</strong> <strong>regeneration</strong> from seedl<strong>in</strong>g roots segments of Brassica oleracea var.Italica .Annuls. Botany 54, 351-361.4. Lazzeri, P.A., Dunwell J.M., 1984 b. Establishment of isolated root culture of Brassica species and <strong>regeneration</strong> fromcultivated roots segments of Brassica oleracea var Italica Annuls Botany 54, 351-361.5. George, L., Rao, P.S., 1980. In-vitro <strong>regeneration</strong> of mustard plant (Brassica juncea var.RAI-5) on cotyledon explants fromnon-irradiated, irradiated and mutagen treated seeds. Annuls Botany46,107-112.6. Chi GL, Pua E C, 1991. Role of ethylene on de-nova <strong>shoot</strong> <strong>regeneration</strong> from cotyledonary explants of Brassica campestrisspp. pekensis (Lour) oisson <strong>in</strong> –vitro. Plant Physiology 96,178-183.7. Dunwell, J.M., 1981. In-vitro <strong>regeneration</strong> from excised leaf disc of Brassica species. Journal of Experimental Botany32,789-799.8. Burbulis N, Bl<strong>in</strong>strubiene A, Kupriene R, Jonytiene V, Rugienius R, Staniene G, (2009). In- vitro <strong>regeneration</strong> of Brassicanapus L. <strong>shoot</strong>s from hypocotyls and stem segments. Zemdirbyste- Agriculture 3, 176-1859. Murashige, T., Skoog. F., 1962. A revised medium <strong>for</strong> rapid growth and bioassay with Tobacco tissue cultures. PlantPhysiology 15, 473-497.10. Stewart, C.N., Adang, M.J., Ali, J.A., Wetal. 1996. Insect control and dosage effect <strong>in</strong> transgenic canola conta<strong>in</strong><strong>in</strong>g a syntheticBacillus thur<strong>in</strong>genensis cry IAC gene. Plant Physiology 112, 115-120.11. Kamal, G.B., Asadollah, A., 2007. Effect of genotype explant type and nutrient medium components on canola (Brassicanapus L.) <strong>shoot</strong> <strong>in</strong> –vitro organogenesis. African Journal of Biotechnology.67, 861-897.12. Koh, W.L., Loh, C.S., 2000. Direct somatic embryogenesis, plant <strong>regeneration</strong> and <strong>in</strong> vitro flower<strong>in</strong>g <strong>in</strong> rapid cycl<strong>in</strong>g Brassicanapus. Plant Cell Report 19, 1177-1183.13. Dietert, M.F., Barron, S.A., Ocvodar, 1982. Effect of genotype on <strong>in</strong>-vitro culture <strong>in</strong> genus Brassica. Plant Science Letters26,233-240.International Journal of Science Innovations and Discoveries VOL1, Issue 2, September-October 2011254

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