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作 者:王姿云[1] 高山林[1] 余伯阳[1] 张剑[1]
出 处:《药物生物技术》2013年第1期26-28,共3页Pharmaceutical Biotechnology
摘 要:为了获得优质品种的兰州百合多倍体,采用鳞片外植体诱导兰州百合(Lilium davidii var.unicolor)试管苗,通过正交实验筛选兰州百合快速繁殖培养基,并对兰州百合鳞茎进行了秋水仙素诱导多倍体的试验研究,还进一步对兰州百合多倍体及二倍体进行了植物抗逆性指标测定。结果表明:兰州百合鳞片能成功诱导出小鳞茎的最佳培养基为MS+PP3332.0 mg/L+BA 1.0 mg/L+NAA 0.1 mg/L+KT 2.0 mg/L,诱导兰州百合多倍体的最佳条件为鳞茎于0.1%秋水仙素溶液浸泡24 h,诱导出的四倍体相比二倍体SOD、POD酶活升高,MDA、脯氨酸含量升高,预示多倍体可能具有较好的抗逆性。In order to select polyploidy of Lilium davidii var. unicolor , the bulb scales were used as explants to induce test-tubeplantlet in vitro. Orthogonal experiment was carried out to establish the best medium composition of rapid propagation in Lilium davidii var. unicolor. Polyploidy was induced by dipping in different concentrations of colchieines. Then resistance index was used to assess the polyploidy. The results indicated that the most suitable medium for bulb propagation was MS + PP3332.0 mg/L + BA1.0 mg/L + NAA0.1 mg/L + KT 2.0 mg/L. The best method of inducing polyploidy was the treatment of immersing the bulbs in colehieines at 0. 1% for 24 h. The test shows that the polyploidy lines of Lilium davidii var. unicolor will have a high resistence with the higher activity of SOD and POD and the higher content of MDA and proline compared with CK. The research indicates that polyploidy may have the greater resistence to the harmful environment.
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