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旋果苣组织培养的研究
引用本文:王薇,钱浩,陈志刚.旋果苣组织培养的研究[J].吉林农业大学学报,2010,32(1):51-53.
作者姓名:王薇  钱浩  陈志刚
作者单位:吉林农业大学园艺学院,长春,130118
基金项目:吉林省科技发展计划项目(20060224)
摘    要:以旋果苣(Streptocarpus wendlanddii)的叶、花葶和花蕾为外植体,以MS为基本培养基,研究了组织培养快繁培养基中细胞分裂素和生长素最佳添加量和不同外植体的最佳灭菌时间。结果表明:在以1 g/L HgCl2溶液进行灭菌时,叶片的最佳灭菌时间是4~5 min,花葶、花蕾的最佳灭菌时间是4 min;在用"84"消毒液进行灭菌时,花葶、花蕾的最佳灭菌时间是5 min。愈伤组织诱导和根分化的最佳培养基均为MS+BA1.0 mg/L+NAA1.0 mg/L;芽分化的最佳培养基为MS+BA4.0 mg/L+NAA0.2 mg/L;继代培养最佳培养基为MS+BA1.0 mg/L+KT0.5 mg/L。

关 键 词:旋果苣    花葶  花蕾  组织培养
收稿时间:2008-10-29
修稿时间:2009-04-16

Studies on Tissue Culture of Streptocarpus wendlanddii
WANG Wei,QIAN Hao,CHEN Zhi-gang.Studies on Tissue Culture of Streptocarpus wendlanddii[J].Journal of Jilin Agricultural University,2010,32(1):51-53.
Authors:WANG Wei  QIAN Hao  CHEN Zhi-gang
Institution:College of Horticulture,Jilin Agricultural University,Changchun 130118,China
Abstract:Leaf, scape and bud of Streptocarpus wendlanddii were used as explants in this study. Based on MS medium, the appropriate approach and sterilization time of tissue culture and rapid propagation of Streptocarpus wendlanddii were obtained via regulating the concentrations of cytokinin and auxin. The results showed that when the explants were sterilized in 1 g/L mercuric chloride, the optimum sterilization time for leaf was 4-5 minutes, while bud was 4 minutes. When the explants were sterilized with 84 disinfectant liquid, the suitable time for scape and bud was 5 minutes. The optimal medium for callus induction was MS+BA 1.0 mg/L+NAA 1.0 mg/L;the optimal medium for bud differentiation was MS+BA 4.0 mg/L+NAA 0.2 mg/L;the optimal medium for root differentiation was MS+BA 1.0 mg/L+NAA 1.0 mg/L;the optimal medium for subculture was MS+BA 1.0 mg/L+KT 0.5 mg/L.
Keywords:Streptocarpus wendlandii  leaf  scape  bud  tissue culture  
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