摘要
目的:以湖南主栽卷丹百合的鳞茎为起始外植体,建立卷丹百合鳞茎高效离体再生体系。方法:比较消毒方法、不同6-BA浓度、培养基组合和环境条件等对鳞茎污染率、不定芽的诱导、伸长和生根的影响。结果:用8%NaClO消毒15 min配合0.1%HgCl_2消毒15~20 min后,消毒效果较好,鳞片成活率高;温度为26±2℃,光照强度为2000 Lx条件下,6-BA浓度为2.5~3.5 mg·L^(-1),鳞片萌芽最快,不定芽生长最健壮;0.5 mg·L^(-1)6-BA+0.2 mg·L^(-1)NAA+1.0 mg·L^(-1)2,4-D培养基组合有利于不定芽的生长;0.5 mg·L^(-1)NAA培养基组合最有利于不定芽的生根,移栽成活率高达100%。结论:建立此体系为卷丹的脱毒苗培育和品种改良提供一定技术支持。
Objective: To establish a high-efficient in vitro regeneration system of bulb scales from Lilium lancifolium using the bulb scales from L. lancifolium as the initial explants. Methods : The effect of sterilization, different concentrations of 6-BA, medium formulations, light intensity and temperature on pollution of bulb scales and induction, elongation and rooting of adventitious buds were compared. Results: The results showed that the optimal sterilization was using 8% NaClO for 15 min and 0. 1% HgCl2 for 15 -20 min. The optimal adventitious buds induction formulation was MS base medium with 2. 5 ~ 3.5 mg·L^-16-BA, and the temperature was 26 ~ 2℃ with 2000 Lx light intensity. The combination of 0. 5 mg·L^-16-BA + 0. 2 mg·L^-1 NAA + 1.0 mg·L^-12, 4-D benefited the elongation of adventitious buds. And 0. 5 mg·L^-1 NAA was the best combination of hormones for rooting, and survival rate of transplanting was 100%. Conclusion: The regeneration system provides a technical support for virus free seedling and variety improvement of L. lancifolium.
出处
《中国现代中药》
CAS
2015年第2期136-140,共5页
Modern Chinese Medicine
基金
湖南省科技厅重点项目(2013NK2008)资助
关键词
湖南
卷丹
鳞片
高效
离体再生
Hunan
Lilium lancifoliium Thunb.
bulb scales
high-efficient
regeneration in vitro