摘要
以MS+6-BA2.0mg/L+IBA0.5mg/L为增殖培养基,1/2MS+IBA0.1mg/L为生根培养基,添加不同浓度的PP333,其结果表明:增殖培养基中添加0.1-0.5mg/LPP333对八仙花试管苗增殖和复壮均有效,而在生根培养基中添加0.05-0.5mg/LPP333有利于生根和移栽,其中以1/2MS+IBA0.1mg/L+PP3330.1mg/L培养基对八仙花试管苗生根和移栽有良好效应。
Added PP333 at different concentrations to proliferative medium and rooting medium when the test tube seedlings of Hydrangea macrophylla were cultured. The medium for proliferation is Ms + 6-BA2.0mg/ L + IBA0.5mg/L. The medium for rooting is 1/2 MS + IBA 0.1mg/L. The results showed that 0.1-0.5 mg/L PP333 improved the proliferation and rejuvenation of the tube-plantlets of the Hydrangea macrophylla, and that 0.05-0.5mg/L PP333 in the medium for rooting improved rooting and transplantation. Among them 1/2 MS + IBA 0.1mg/L + PP3330.1mg/L was most effective.
出处
《中国农学通报》
CSCD
2005年第4期56-58,共3页
Chinese Agricultural Science Bulletin
基金
湖南省衡阳市科技攻关项目--实用植物离体快速繁殖技术研究(2002-15-21)
