DIRECT SOMATIC EMBRYOGENESIS THROUGH THIN CELL LAYER CULTURE IN PANAX-GINSENG

Direct somatic embryos were differentiated on cotyledon transverse Thi n Cell Layers (tTCLs) of Panax ginseng after 9 weeks in the Murashige and Skoog basal (MS) medium containing 2,4-D (5 mu M). When MS medium containing 2,4-D (5 mu M) was used for seedling pretreatment and for t TCLs culture, somatic embryos were observed 2 weeks earlier i.e. after 7 weeks of culture. On the tTCLs from seedlings pretreated with 2,4-D (5 mu M) combined with benzyladenine and zeatin at 0.1 mu M (BZ), som atic embryos were observed after 6 weeks of culture and the percentage of embryogenesis was higher (62%) than when 2,4-D was used alone for pretreatment (40%). Similar results were also obtained from pretreatme nt with combinations of 2,4-D (5 mu M) and thidiazuron (TDZ) (0.01, 0. 1 mu M). When a combination of 2,4-D (5 mu M) and BZ (0.1 mu M) was us ed both for seedling pretreatment and for tTCLs culture, both somatic embryos and shoots were observed after only 3 weeks. As the concentrat ion of BZ increased, the percentage of somatic embryogenesis decreased but the percentage of organogenesis increased. Similar responses were obtained with a combination of 2,4-D (5 mu M) and TDZ (0.01 mu M) On the medium containing both NAA (0.3 mu M) and BZ (1 mu M), globular- a nd heart- stage embryos developed after 4 weeks of culture into cotyle donary-staged embryos which remained dormant after a short elongation of the embryo axis. The importance of seedling pretreatment by growth substances in enhancing somatic embryogenesis is reported.