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贴梗海棠组培快繁技术研究
引用本文:陈罡,叶景丰,马冬菁,潘文利,范俊岗. 贴梗海棠组培快繁技术研究[J]. 北方园艺, 2008, 0(8)
作者姓名:陈罡  叶景丰  马冬菁  潘文利  范俊岗
作者单位:辽宁省林业科学研究院,辽宁,沈阳,110032
基金项目:沈阳市科技局农业应用技术攻关资助项目
摘    要:以贴梗海棠带芽茎段为材料,研究了贴梗海棠组织培养和快速繁殖的适宜条件,结果表明:茎尖和半木质化茎段在MS 6-BA 1 mg/L NAA 0.2 mg/L中的诱导率均在90%以上;筛选出的最佳继代增殖培养基为:MS 6-BA 0.5 mg/L NAA 0.5 mg/L,增殖系数为7.2;生根培养基为:1/2 MS IBA 0.3 mg/L NAA 0.2 mg/L,生根率达93%.

关 键 词:贴梗海棠  组织培养  快速繁殖

Studies on Tissue Culture and Rapid Propagation Technique of Chaenomeles speciosa(sweet)Nakai
CHEN Gang,YE Jing-feng,MA Dong-jing,PAN Wen-li,FAN Jun-gang. Studies on Tissue Culture and Rapid Propagation Technique of Chaenomeles speciosa(sweet)Nakai[J]. Northern Horticulture, 2008, 0(8)
Authors:CHEN Gang  YE Jing-feng  MA Dong-jing  PAN Wen-li  FAN Jun-gang
Abstract:By using stems with buds of Chaenomeles speciosa(sweet)Nakai as materials,the experiment was made to find out the best culture process and proper culture medium.The technical system of tissue culture for rapid propagation was established.The results were as follows:The rate of initiation of shoot apex and half-lignification stems in MS 6-BA 1mg/L NAA 0.2mg/L were all over 90%;The optimal subculture medium was MS 6-BA 0.5mg/L NAA 0.5mg/L,the multiplication rate of shoot clumps could be up to 7.2;The proper rooting medium was 1/2 MS IBA 0.3mg/L NAA 0.2mg/L,and the rooting rate could be up to 93%.
Keywords:Chaenomeles speciosa(sweet)Nakai  Tissue culture  Rapid propagation
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