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BA0.5~1.0mg·L^-1 +NAA0.5mg·L^-1,适于丛生芽的诱导与增殖;附加LAA 1.0mg·L^-1 + BA3mg·L^-1,适于愈伤组织的诱导;附加姒1.0mg·L^-1 +BA2.0~3.0mg·L^-1适于愈伤组织继代培养,附加BA2.0mg·L^-1+NAA0.5mg·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。
Objective: To provide scientific basis for large scale production by studying the technique of tissue culture of Gentiana stramines. Method: Callus was induced from germ-free stem segment of G. stramines on a MS medium supplemented with different hormones. Result: The MS medium with 0.5-1.0mg·L^-1 BA and 0.5 mg·L^-1 NAA was suitable for the induction and proliferation of cluster bads. MS medium with 1.0 mg·L^-1 IAA and 3 mg·L^-1 BA was suitable for the induction of calli. MS medium with 1.0 mg·L^-1 IAA and 2,0-3.0mg·L^-1 BA was suitable for the subculture of calli. MS medium with 2.0mg·L^-1 BA and 0.5mg·L^-1 NAA was suitable for the differentiation of calli. Condutton: Aseptic seeding of G. stramiess can be quickly propagated by shoot culture.
出处
《中国中药杂志》
CAS
CSCD
北大核心
2006年第10期797-800,共4页
China Journal of Chinese Materia Medica
基金
甘肃省环保局项目(GH2001-10)
关键词
麻花秦艽
组织培养
植株再生
Gerulana stramines
tissue culture
plant regeneration