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郁金香组培快繁技术研究
引用本文:田英翠,袁雄强.郁金香组培快繁技术研究[J].安徽农业科学,2006,34(2):227-227,232.
作者姓名:田英翠  袁雄强
作者单位:1. 中南林学院,湖南,长沙,410004
2. 湖南省长沙市园林科学研究所,湖南,长沙,410003
基金项目:湖南省自然科学基金,中南林学院青年基金重点项目资助
摘    要:以郁金香的鳞片、茎段和茎尖为外植体进行了组培快繁技术研究,筛选出最佳培养基。诱导鳞片产生丛芽:MS+0.4~1.0 mg/LBA+0.4 mg/LNAA;诱导茎尖产生丛芽:MS+2 mg/LBA+0.1 mg/LNAA;诱导茎段产生丛芽:MS+1.0 mg/LBA+0.2 mg/LNAA;丛芽增殖培养:MS+0.4 mg/LBA+0.2 mg/LNAA和MS+0.4 mg/LBA+0.2 mg/LIAA;茎类丛芽生根诱导培养:1/2 MS+0.4 mg/LKT和0.1~1.0 mg/LNAA。

关 键 词:郁金香  组织培养  激素
文章编号:0517-6611(2006)02-0227-01
收稿时间:2005-11-14
修稿时间:2005-11-14

Study on Techniques of Rapid Propagation by Tissue Culture of Tulipa cvs
TIAN Ying-cui et al.Study on Techniques of Rapid Propagation by Tissue Culture of Tulipa cvs[J].Journal of Anhui Agricultural Sciences,2006,34(2):227-227,232.
Authors:TIAN Ying-cui
Institution:Central South Forestry University,Changsha,Hunan 410004
Abstract:The clone propagation of Tulipa cvs is developed through culture of scales and stems in vitro.The results showed that the best media for various stages were as follows:inducation medium of shoots is MS+0.4~1.0 mg/L BA+0.4 mg/L NAA,MS+2 mg/L BA+0.1 mg/L NAA and MS+1.0 mg/L BA+0.2 mg/L NAA;proliferation medium is MS+0.4 mg/L BA+0.2 mg/L NAA and MS+0.4 mg/L BA+0.2 mg/L IAA.;Induction of roots is better in medium of 1/2 MS+0.4 mg/L KT+0.1~1.0 mg/L NAA.
Keywords:Tulipa cvs  Tissue culture  Phytohormone  
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