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人参果组织培养技术研究
引用本文:张俊伟,郭盘江,陈冠吉.人参果组织培养技术研究[J].西南林学院学报,2003,23(2):21-22.
作者姓名:张俊伟  郭盘江  陈冠吉
作者单位:西南林学院,资源学院,云南,昆明,650224
基金项目:云南省省级重点建设专业西南林学院林学专业资助
摘    要:以人参果的幼嫩茎段和叶片作外植体,在MS基本培养基附加不同浓度6-BA IAA,6-BA NAA 和 KT 2,4 D 组成的固体培养基中进行培养.结果显示:MS 6-BA 0.07 mg/L IAA 0.03mg/L,MS 6-BA 0.70mg/L IAA 0.03mg/L,MS 6-BA 0.70mg/L IAA O.05mg/L,MS 6-BA 1.00mg/L IAA 0.05mg/L 4种培养基中的材料愈伤组织长势比较好,分化明显、经继代培养,丛生芽大量形成,丛生苗根系发达、其他培养基则停留在愈伤组织阶段或只长出极少数短的根.

关 键 词:人参果  组织培养  幼嫩茎段  叶片  外植体  培养基
文章编号:1003-7179(2003)02-0021-02

A Study on Culture Technology of Tissue of Solanum muricatum
ZHANG Jun-wei,GUO Pan-jiang,CHEN Guan-ji.A Study on Culture Technology of Tissue of Solanum muricatum[J].Journal of Southwest Forestry College,2003,23(2):21-22.
Authors:ZHANG Jun-wei  GUO Pan-jiang  CHEN Guan-ji
Abstract:The delicate stem cuttings of Solanum muricatum. were inoculated on MS base medium supplied with different concentrations of 6-BA and IAA. The results showed that, the differentiation of callus on the MS+6-BA 0.07mg/L+IAA 0.03 mg/L, MS+6-BA 0.70 mg/L + IAA 0.03 mg/L,MS+6-BA 0.70 mg/L+IAA 0.05 mg/L,MS+6-BA 1.00 mg/L+IAA 0.05 mg/L were obvious. By continuing culture, the number of roots increased and grew well.The other stem cuttings were difficult to induced to callus or few roots were induced
Keywords:Solanum muricatum  tissue culture  callus
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