首页 | 本学科首页   官方微博 | 高级检索  
     

TDZ和6-BA对大豆子叶节再生体系中丛生芽诱导的效应
引用本文:聂王星,於丙军. TDZ和6-BA对大豆子叶节再生体系中丛生芽诱导的效应[J]. 南京农业大学学报, 2012, 35(4): 130-134
作者姓名:聂王星  於丙军
作者单位:南京农业大学生命科学学院,江苏南京,210095
基金项目:国家自然科学基金,国家转基因生物新品种培育重大专项
摘    要:以栽培大豆品种‘Jackson’为试材,用萌发5 d的子叶节作外植体,接种于不同激素配比的萌发培养基和诱导培养基中,分析和比较TDZ(噻二唑苯基脲)和6-BA(6-苄基腺嘌呤)单独和复配使用时对大豆子叶节再生体系中丛生芽的诱导效应,并对其优化组合进行了筛选。结果表明:在种子萌发培养基中,0.5 mg·L-16-BA或TDZ单独使用时,前者能使丛生芽诱导率达到75.56%,诱导效应好于后者,但每个子叶节出芽数低于后者。在诱导培养基中,0.5 mg·L-16-BA和1.0 mg·L-1TDZ复配使用时,丛生芽诱导率最高且每个子叶节出芽数最多,分别为84.75%和3.04。

关 键 词:大豆  子叶节  丛生芽  TDZ  6-BA

Effects of TDZ and 6-BA on inducing multiple shoots in soybean cotyledonary node regeneration system
NIE Wang-xing , YU Bing-jun. Effects of TDZ and 6-BA on inducing multiple shoots in soybean cotyledonary node regeneration system[J]. Journal of Nanjing Agricultural University, 2012, 35(4): 130-134
Authors:NIE Wang-xing    YU Bing-jun
Affiliation:(College of Life Sciences,Nanjing Agricultural University,Nanjing 210095,China)
Abstract:The soybean cultivar "Jackson" was used as the experimental material in this study.The soybean cotyledonary nodes from germinated seeds for 5 d were used as the explant and inoculated onto the different culture media for seed germination and multiple shoot induction.The different effects of TDZ(thidiazuron),6-BA(6-benzyladenine)and their optimized combination on inducing multiple shoots in soybean cotyledonary node regeneration system were investigated.The results showed that,when 0.5 mg·L-1 6-BA or TDZ was separately added to the seed germination medium,the regeneration rate of multiple shoots for the former could reach 75.56%,which was higher than the latter,but the budding number of each cotyledonary node showed the reverse.When 0.5 mg·L-1 6-BA and 1.0 mg·L-1 TDZ were simultaneously added to the induction medium,the regeneration rate of multiple shoots and the budding number of each cotyledonary node could reach 84.75% and 3.04 at the maximum level,respectively.
Keywords:soybean  cotyledonary node  multiple shoots  TDZ  6-BA
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号