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麻花秦艽组织培养及植株再生的研究
引用本文:刘丽莎,张西玲,王岚,张延红.麻花秦艽组织培养及植株再生的研究[J].中国中药杂志,2006,31(10):797-800.
作者姓名:刘丽莎  张西玲  王岚  张延红
作者单位:甘肃中医学院,甘肃,兰州,730000
摘    要:目的:研究药用植物麻花秦艽组织培养技术,为工厂化育苗提供科学依据。方法:以麻花秦艽根、茎育出的无菌苗为外植体,采用MS培养基,附加不同的植物激素进行实验。结果:以MS培养基为基本培养基,附加BA 0.5~1.0 mg·L-1+NAA 0.5 mg·L-1,适于丛生芽的诱导与增殖;附加IAA 1.0 mg·L-1+BA 3 mg·L-1,适于愈伤组织的诱导;附加IAA 1.0 mg·L-1+BA 2.0~3.0 mg·L-1适于愈伤组织继代培养,附加BA 2.0 mg·L-1+NAA 0.5 mg·L-1适于愈伤组织的分化。结论:通过诱导愈伤组织途径可以达到快速繁殖的目的。

关 键 词:麻花秦艽  组织培养  植株再生
文章编号:1001-5302(2006)10-0797-04
收稿时间:2/1/2004 12:00:00 AM
修稿时间:2004-02-01

Studies on plantlet regeneration and propagation of Gentiana stramines
LIU Li-sha;ZHANG Xi-ling;WANG Lan;ZHANG Yan-hong.Studies on plantlet regeneration and propagation of Gentiana stramines[J].China Journal of Chinese Materia Medica,2006,31(10):797-800.
Authors:LIU Li-sha;ZHANG Xi-ling;WANG Lan;ZHANG Yan-hong
Institution:Gansu College of Traditional Chinese Medicine, Lanzhou 730000, China.
Abstract:Objective:To provide scientific basis for large scale production by studying the technique of tissue culture ofGentiana stramines.Method:Callus was induced from germ-free stem segment ofG.stramineson a MS medium supplemented with different hormones.Result:The MS medium with 0.5-1.0 mg.L-1BA and 0.5 mg.L-1NAA was suitable for the induction and proliferation of cluster bads.MS medium with 1.0 mg.L-1IAA and 3 mg.L-1BA was suitable for the induction of calli.MS medium with 1.0 mg.L-1IAA and 2.0-3.0 mg.L-1BA was suitable for the subculture of calli.MS medium with 2.0 mg.L-1BA and 0.5 mg.L-1NAA was suitable for the differentiation of calli.Conclution:Aseptic seeding ofG.straminescan be quickly propagated by shoot culture.
Keywords:Gentiana stramines  tissue culture  plant regeneration
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