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龙牙蕉组织培养技术
引用本文:陈桂平,陈德华,曾少敏,廖玉章,廖鉴湖,杨惠文.龙牙蕉组织培养技术[J].广西园艺,2009,20(2):10-11.
作者姓名:陈桂平  陈德华  曾少敏  廖玉章  廖鉴湖  杨惠文
作者单位:汕头市果树研究中心,广东,汕头,515041  
摘    要:龙牙蕉吸芽茎尖经MS+6-BA5.0mg/L+AD20mg/L培养基诱导出不定芽后,在MS+BA4mg/L+NAA0.1mg/L培养基上继代培养对不定芽的分化较好,平均分化倍数为2.6倍以上,无根小苗在1/2MS+NAA0.5mg/L+AC1g/L培养基上进行生根培养,1周后长出新根。组培小苗移栽假植成活率94%,大田栽培表现正常。

关 键 词:龙牙蕉  组织培养  细胞分裂素

The technique of tissue culture for Musa spp.Longyajiao
CHEN Gul-ping,CHEN De-hua,ZENG Shao-ming,LIAO Yu-zhang,LIAO Jian-hu,YANG Hui-wen.The technique of tissue culture for Musa spp.Longyajiao[J].Guangxi Horticulture,2009,20(2):10-11.
Authors:CHEN Gul-ping  CHEN De-hua  ZENG Shao-ming  LIAO Yu-zhang  LIAO Jian-hu  YANG Hui-wen
Institution:CHEN Gul-ping,CHEN De-hua,ZENG Shao-ming,LIAO Yu-zhang,LIAO Jian-hu,YANG Hui-wen(Shantou Fruit Research Center,Shantou 515041 China)
Abstract:Adventitious buds were induced from shoot-tip explants of Musa spp Longyajiao in MS+6-BA5.0 mg/L+AD 20 mg/L.The multiplication medium with MS+BA 4 mg/L+NAA 0.1 mg/L was better for the buds growth and the average multiplication rate was over 2.6 times.Plantlets were cultured on 1/2 MS+NAA 0.5 mg/L+AC 1 g/L,for rooting culture,after 7 days the roots of the plantlets were developed.The regenerated plantlets were transplanted to soil,and the survival rat of transplanting reached 94%.The plants grew well in the ...
Keywords:Musa spp Longyajiao  Tissue culture  Cytokinin  
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