Yan Zhang, Xiuying Zhang, Yuxuan Xie, Zebin Lin, Boyi Chen, B. Cai
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引用次数: 0
摘要
通过对鳞茎球形蝶(Sphaeropteris lepifera)的无菌培养试验。例钩)。R. M. Tryon,尝试筛选出细绒球孢子无菌培养各工序的最佳条件,以期建立系统、高效、完整的细绒球孢子无菌培养技术体系,尝试实现细绒球苗的工厂化生产。以细球(Sphaeropteris lepifera)叶片上的成熟深褐色孢子为外植体,75%酒精消毒10 s, 0.1% Hg消毒6 min,诱导萌发培养基为1/ 5ms +6- ba 0.5 mg/L+IBA 0.5 mg/L。增殖培养基为1/ 2ms + 6-BA 0.3 mg/L+ IBA 0.05 mg/L。分化培养基为MS+6-BA 0.05 mg/L+ IBA 0.05 mg/L。生根培养基为MS + 6-BA 0.2 mg/L + IBA 0.2 mg/L。培养温度为(25±2)℃,光源为荧光,光照时间为12 h/d,光照强度为2000 lx。
Construction of Aseptic Culture System for Spores of Sphaeropteris lepifera
Through the aseptic culture test of Sphaeropteris lepifera (J Sm. ex Hook.) R. M. Tryon, try to screen out the best conditions for each process of aseptic culture for spores of Sphaeropteris lepifera, in order to establish a systematic, efficient and complete aseptic culture technology system for spores of Sphaeropteris lepifera, and try to achieve factory production of Sphaeropteris lepifera seedlings. The mature dark brown spores off leaf from Sphaeropteris lepifera were used as explants, disinfected with 75% alcohol for 10 s and 0.1% Hg for 6 min. The induced germination medium is 1/5 MS+6-BA 0.5 mg/L+IBA 0.5 mg/L. The proliferation medium is 1/2 MS + 6-BA 0.3 mg/L+ IBA 0.05 mg/L. The differentiation medium is MS+6-BA 0.05 mg/L+ IBA 0.05 mg/L. And the rooting medium is MS + 6-BA 0.2 mg/L + IBA 0.2 mg/L. The culture temperature is (25±2)°C, the light source is fluorescent, the illumination time is 12 h/d, and the illumination intensity is 2000 lx.