天然产物研究与开发 ›› 2016, Vol. 28 ›› Issue (3): 350-353.doi: 10.16333/j.1001-6880.2016.3.005

• 研究论文 • 上一篇    下一篇

大苞短毛唇柱苣苔离体培养和快速繁殖

文弢,娄丽,侯娜*,李从瑞,王莲辉   

  1. 贵州省林业科学研究院,贵阳 550005
  • 出版日期:2016-03-30 发布日期:2016-04-07

In vitro Culture and Rapid Propagation of Chirita brachytricha var. magnibracteata W.T.Wang et D.Y.Chen

WEN Tao,LOU Li,HOU Na*,LI Cong-rui,WANG Lian-hui   

  1. Guizhou Academy of forestry,Guiyang 550005,China
  • Online:2016-03-30 Published:2016-04-07

摘要: 为了探索大苞短毛唇柱苣苔离体培养和快速繁殖的最佳培养条件。以大苞短毛唇柱苣苔叶片为外植体,建立其组培快繁再生体系。结果表明大苞短毛唇柱苣苔叶片外植体的最优消毒方法为:采用75%酒精灭菌15 s,0.1%HgCl2灭菌4 min;叶片诱导不定芽最佳培养基为:MS+TDZ0.5 mg/L+NAA0.1 mg/L,诱导率为83.75%;不定芽增殖最佳培养基为MS+6-BA0.5 mg/L+NAA0.1 mg/L,增殖系数可达16,且不定芽生长良好;生根培养基以1/2MS+IBA0.1 mg/L为最好,生根率达96.67%以上。组培苗经炼苗及移栽,成活率达95%以上。建立了大苞短毛唇柱叶片组织培养的快繁体系,为规模化生产大苞短毛唇柱苣苔提供技术指导。

关键词: 大苞短毛唇柱苣苔, 离体培养, 快速繁殖

Abstract: In this study,the condition of in vitro culture and rapid propagation of Chirita brachytricha.var. magnibracteata W.T.Wang et D.Y.Chen was investigated with its leaves as explants.The effects of different hormones for callus induction and plant regeneration of leaves were studied.The results showed that:the optimal way to obtain sterile explant for leaves were sterilized in 75% ethyl alcohol for15 s then 0.1% HgCl2 for 4 min;The optimal medium for callus of leaves was MS+TDZ0.5 mg/L+NAA0.1 mg/L,induction rate was 83.75%;The optimal medium of induction of adventitious buds was MS+6-BA0.5 mg/L+NAA0.1 mg/L,Multiplication factor was 16,and seedlings grew well;The optimal medium and plant growth substances combination for rooting induction was 1/2MS+IBA0.1 mg/L;Rooting rate was 96.67%.Transplant survival rate of plantlet reached more than 95%.In conclusion,the condition of plant regeneration and clonal propagation system was established.It provided technical guidance for production of C.brachytricha.var.magnibracteata W.T.Wang et D.Y.Chen.

Key words: Chirita brachytricha.var. magnibracteata W.T.Wang et D.Y.Chen, in vitro  culture;rapid propagation

中图分类号: 

S731