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The study aimed to optimize the induction and differentiation medium by exploreing different tissue culture of Saposhnikovia divaricata (Turcz.) Schischk. In tissue culture with the root, stem segments, young leaf, cotyledonary node and axillary bud of Saposhnikovia divaricata (Turcz.) Schischk as explants, a lot of plantleles were obtained and the corresponding plant regeneration-system was established. The results showed that when use MS+1.0 mg · L-1 6-BA +0.2 mg · L-1 NAA as callus induction medium, the cotyledonary node had the highest bourgeon rate, and its callus was better than any others; MS +2 mg · L-1 6-BA +0.4 mg · L-1 NAA was the best adventitious buds induction medium, and the best adventitious buds induced condition was 3% sucrose as carbon source, illumination for 12-14 h · d-1 and pH 5.8. The best rootage medium was 1/2 MS+0.5 mg · L-1 NAA.
The study aimed to optimize the induction and differentiation medium by explore different tissue culture of Saposhnikovia divaricata (Turcz.) Schischk. In tissue culture with the root, stem segments, young leaf, cotyledonary node and axillary bud of Saposhnikovia divaricata (Turcz.) Schischk as explants, a lot of plantleles were obtained and the corresponding plant regeneration-system was established. The results showed that when use MS + 1.0 mg · L-1 6-BA +0.2 mg · L -1 NAA as callus induction medium, the cotyledonary node had the highest bourgeon rate, and its callus was better than any others; MS +2 mg · L-1 6-BA +0.4 mg · L-1 NAA was the best adventitious buds induction medium, and the best adventitious buds induced The condition was 3% sucrose as carbon source, illumination for 12-14 h · d-1 and pH 5.8. The best rootage medium was 1/2 MS + 0.5 mg · L -1 NAA.