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水半夏组培快繁体系的建立
引用本文:丁 伟,张立红,潘晟昊,陈集双.水半夏组培快繁体系的建立[J].医学教育探索,2011,42(3):585-588.
作者姓名:丁 伟  张立红  潘晟昊  陈集双
作者单位:1. 浙江理工大学 生物工程研究所, 浙江 杭州 310018 2. 南京工业大学 生物资源研究所, 江苏 南京 210009
基金项目:国家“863”基金项目(2002AA241121)
摘    要:目的 建立水半夏的组培快繁体系,为快速、大量生产水半夏种苗提供基础。方法 利用不同植物激素配比的培养基,以水半夏块茎为外植体进行试验。结果 愈伤培养基MS+NAA 0.2 mg/L+KT 1.0 mg/L+蔗糖3 %+琼脂6 g/L可成功诱导水半夏愈伤组织;丛生芽培养基MS+NAA 0.2 mg/L+6-BA 2.0 mg/L+蔗糖3 %+琼脂6 g/L诱导不定芽效果较好,增殖倍数高;生根培养基1/2 MS+NAA 0.2 mg/L+IBA 0.4 mg/L+KT 0.2 mg/L+蔗糖3 %+琼脂6 g/L+AC 0.3 g/L,有利于水半夏不定根的快速形成,12~14周即可获得再生水半夏植株。培养基MS+NAA 0.2 mg/L+6-BA 1.5 mg/L+蔗糖3 %+琼脂6 g/L为诱导水半夏分化一次性成苗的最佳激素配比,5~6周可形成试管苗,10周后可用于炼苗。结论 建立的水半夏组培快繁体系为水半夏优良品种的快速繁殖奠定基础,且可应用于工厂化生产水半夏种苗。

关 键 词:水半夏  组织培养  一次性成苗  快速繁殖  植物激素

Establishment of tissue culture and rapid propagation system of Typhonium flagelliforme
DING Wei,ZHANG Li-hong,PAN Sheng-hao,CHEN Ji-shuang.Establishment of tissue culture and rapid propagation system of Typhonium flagelliforme[J].Researches in Medical Education,2011,42(3):585-588.
Authors:DING Wei  ZHANG Li-hong  PAN Sheng-hao  CHEN Ji-shuang
Institution:1. Institute of Bioengineering, Zhejiang Sci-Tech University, Hangzhou 310018, China 2. Institute of Bioresource Engineering, Nanjing University of Technology, Nanjing 210009, China
Abstract:Objective To establish the rapid propagation system and tissue culture techniques of Typhonium flagelliforme for large-scale seedlings. Methods Using media with different hormones proportions, the tuber tissue was found to be a good explant for inducing asexual propagation system. Results The callus culture medium consisted of MS+NAA 0.2 mg/L+KT 1.0 mg/L+sucrose 3%+agar 6 g/L could generate callus successfully. Medium consisted of MS+NAA 0.2 mg/L+6-BA 2 mg/L+sucrose 3 % + agar 6 g/L was a superlative proportion of hormones concentration to generate adventitious buds efficiently, especially for higher proliferated multiples. The rooting medium consisted of 1/2 MS+NAA 0.2 mg/L+IBA 0.4 mg/L+KT 0.2 mg/L+sucrose 3 %+agar 6 g/L+AC 0.3 g/L was conducive to generate roots rapidly. The explants could be acclimatized after a period of 12 to 14 weeks. Experiments of one-step-seedling formation indicated that the one-step-seedling formation medium, containing MS+NAA 0.2 mg/L+6-BA 1.5 mg/L+sucrose 3%+agar 6 g/L was the best proportion of hormone concentration, for 5 to 6 weeks, new plantlets could be developed, which will be acclimatized in 10 weeks. Conclusion The tissue culture techniques and rapid propagation system of T. flagelliforme could be used for large-scale seedlings and lay a foundation for its improved breeds.
Keywords:Typhonium flagelliforme (Lodd  ) Blume  tissue culture  one-step-seedling formation  rapid propagation  plant hormone
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