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大根唇柱苣苔的组培快繁技术
引用本文:林茂,李进华,唐庆,王华新,廖美兰,龙定建.大根唇柱苣苔的组培快繁技术[J].热带作物学报,2017(3):508-512.
作者姓名:林茂  李进华  唐庆  王华新  廖美兰  龙定建
作者单位:广西壮族自治区林业科学研究院,广西南宁,530002
基金项目:广西林业科技项目(桂林科字2013第5号),广西自然科学基金项目(2014GXNSFBA118091),国家林业局部门预算广西项目(桂林护预2015007),广西壮族自治区林业科学研究院基本科研业务费项目(林科201405号)
摘    要:以大根唇柱苣苔叶片为外植体,以MS为基本培养基,附加不同种类和浓度的激素进行组培快繁技术研究。结果表明:适宜叶片不定芽诱导的培养基是MS+6-BA 1.00 mg/L+NAA 0.05 mg/L,继代增殖培养的适宜培养基为MS+6-BA 1.50~3.00 mg/L+NAA 0.10 mg/L,适宜的生根培养基为1/2MS+IBA 0.20~0.30 mg/L,适宜的基质是泥炭∶珍珠岩=2∶1、泥炭∶细河沙=2∶1、泥炭∶园土=2∶1。

关 键 词:大根唇柱苣苔  组培  快繁  不定芽

Tissue Culture and Rapid Regeneration of Chirita macrorhiza
LIN Mao,LI Jinhua,TANG Qing,WANG Huaxin,LIAO Meilan,LONG Dingjian.Tissue Culture and Rapid Regeneration of Chirita macrorhiza[J].Chinese Journal of Tropical Crops,2017(3):508-512.
Authors:LIN Mao  LI Jinhua  TANG Qing  WANG Huaxin  LIAO Meilan  LONG Dingjian
Abstract:The leaf of Chirita macrorhiza was used as the explants and cultured on MS medium supplemented with different concentrations of plant hormones.The results showed that:the adventitious bud induction culture medium was MS+6-BA 1.00 mg/L+NAA 0.05 mg/L.The shoots proliferation medium was MS+6-BA 1.50-3.00 mg/L+NAA 0.10 mg/L.The root induction medium was 1/2MS+IBA 0.20-0.30 mg/L.The suitable ratio of transplanting medium for peat ∶ perlite was 2 ∶ 1,peat ∶ fine sand is 2 ∶ 1,and peat ∶ soil was 2 ∶ 1.
Keywords:Chirita macrorhiza  tissue culture  rapid regeneration  adventitious bud
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