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朱砂根的组织培养与植株再生 被引量:9

Tissue culture and plant regeneration of Ardisia crenata
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摘要 目的:研究药用植物朱砂根组培快繁技术,为其产业化生产提供科学依据。方法:考察不同基本培养基、植物激素、添加物等对腋芽诱导、增殖及植株再生的影响。结果:以朱砂根带芽茎段为外植体,初代培养腋芽诱导的最佳培养基为MS+6-BA 0.5 mg.L-1+NAA 0.1 mg.L-1。腋芽增殖的最佳培养基配方为MS+6-BA 2.0 mg.L-1+NAA 0.1 mg.L-1+KT 0.5 mg.L-1。生根培养基为1/2MS+IBA 0.2 mg.L-1;添加0.2%的活性炭可明显促进根的生长,提高生根率、生根数。最有利于朱砂根无菌苗移栽存活的基质类型为河沙-珍珠岩-蛭石(1∶1∶1),或蛭石-珍珠岩(1∶1),成活率在80%以上。结论:通过腋芽增殖快繁育苗技术可获得完整植株,达到快速繁殖的目的。 Objective: Our research studied the fast-breeding technology of Ardisia crenata sims by using tissue culture and provided the scientific foundation for industry production. Method: The effects of axillary buds and plant regeneration of different basic medium, hormones and additives on induction and multiplication were studied. Result: The best culture medium for the induction of axillary buds, which took the stems of A. crenate were as explants, was MS + 6-BA 0.5 mg·L^-1 + NAA 0. 1 mg·L^-1 , and the best medium for multiplication was MS + 6-BA 2.0 mg·L^-1 + NAA 0. 1 mg·L^-1 + KT 0. 5 mg·L^-1, the best medium for roots generation was 1/2MS + IBA 0. 2 mg·L^-1. We also found that the roots'generation, roots rate and mean number of roots can be promoted by adding 0. 2% Ac, and the most suitable ground substance was river sand-perlite-vermiculite ( 1 : 1 : 1 ) or perlite-vermiculite ( 1 : 1 ). With axillary buds and plant regeneration methode, more than 80% A. crenata sims could be regenerated integratedly. Conclusion: A. crenata sims can be regenerated integratedly and breeded fast by using axillary bud proliferation technology.
出处 《中国中药杂志》 CAS CSCD 北大核心 2009年第16期2043-2046,共4页 China Journal of Chinese Materia Medica
基金 四川省教育厅攻关项目(2006A016)
关键词 朱砂根 组织培养 植株再生 Ardisia crenata tissue culture plant regeneration
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