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黄山药愈伤组织诱导与分化
引用本文:张玲,马林,杨国涛.黄山药愈伤组织诱导与分化[J].生物技术,2005,15(3):70-73.
作者姓名:张玲  马林  杨国涛
作者单位:西南科技大学生命科学与工程学院,四川,绵阳,621002
基金项目:四川省教育厅重点课题(2003A122)
摘    要:采用黄山药野生植株作为外植体,试验了不同激素处理对黄山药愈伤组织的诱导、分化影响,结果表明:不同的外植体的诱导率差别较大,叶片的诱导率最高,最高达到85.7%,茎段的诱导率较低,平均诱导率仅10%左右。以叶片作为外植体诱导愈伤组织的最佳培养基配方为MS 2,4-D2.0mg/L 6-BA2.5mg/L;愈伤组织分化生芽的最佳配方为MS BA1.0mg/L NAA0.5mg/L 蔗糖2% pH6.4;愈伤组织分化生根的最佳配方诱MS BA1.0mg/L NAA0.1mg/L 蔗糖3% pH6.80。

关 键 词:黄山药  愈伤组织  诱导  分化

Callus Induction and Differentiation of Dioscorea panthaica
ZHANG Ling,MA Lin,YANG Guo-tao.Callus Induction and Differentiation of Dioscorea panthaica[J].Biotechnology,2005,15(3):70-73.
Authors:ZHANG Ling  MA Lin  YANG Guo-tao
Abstract:The Dioscorea panthaica callus induction and differentiation were studied with different hormones when it used the wild Dioscorea panthaica as explant. The result showed: Different explants would bring great difference of the induction rate, the induction rate of the blade was the highest, up to 85 .7%, the induction rate of the stem was relatively low, only about 10% equally. When it used blade as explant, the best callus induction formula was 2.0ml/L 2,4-D and 2.5ml/L 6-BA were added in the MS culture medium, the best bud differentiation formula was 0.5ml/L NAA and 1.0ml/L BA were added in the MS medium, with 2% sugar at pH6.4. And the root differentiation rate was highest when 0.1ml/L NAA and 1.0ml/L BA were added in it,with 3% sugar at pH6.8.
Keywords:Dioscorea panthaica  callus  induction  differentiation
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