首页 | 本学科首页   官方微博 | 高级检索  
     

非洲紫罗兰叶片外植体再生技术体系的建立
引用本文:程云清,刘剑锋,钟雪,陈智文. 非洲紫罗兰叶片外植体再生技术体系的建立[J]. 中国农学通报, 2010, 26(10): 212-216
作者姓名:程云清  刘剑锋  钟雪  陈智文
作者单位:吉林师范大学生态环境研究所,吉林四平,136000
摘    要:以三种叶型的非洲紫罗兰(Saintpaulia ionantha)叶片作为外植体材料,研究了叶片外植体再生技术体系。结果表明:非洲紫罗兰叶片愈伤组织诱导的最佳培养基为MS+6-BA 0.5 mg/L+NAA 0.3 mg/L和MS+6-BA 0.5 mg/L+NAA 0.5mg/L,培养4周左右,诱导率达100%,绝大多数愈伤组织上都有芽的分化。采用培养基MS+6-BA 0.5 mg/L+NAA 0.3 mg/L继代一次后,每个愈伤组织上分化产生的芽可达30余个,3个品种的愈伤组织诱导、成芽能力差异不大。非洲紫罗兰品种A和C适宜的生根培养基为1/2MS+0.2mg?L-1NAA,品种B适宜的生根培养基为1/2MS+0.5mg?L-1IBA。生根苗转入纯蛭石栽培时,用1/4MS大量与微量元素进行叶片追肥,成活率90%以上。移栽至腐殖土栽培成活率95%以上,3个月栽培后栽培苗成花。本研究为非洲紫罗兰试管苗的工厂化生产提供了科学依据。

关 键 词:荣宝  荣宝  土壤消毒  作物产量  效益  影响  
收稿时间:2009-12-21
修稿时间:2010-01-10

Tissue Culture and Regeneration System from Leaves of Saintpaulia ionantha in vitro
Cheng Yunqing,Liu Jianfeng,Zhong Xue,Chen Zhiwen. Tissue Culture and Regeneration System from Leaves of Saintpaulia ionantha in vitro[J]. Chinese Agricultural Science Bulletin, 2010, 26(10): 212-216
Authors:Cheng Yunqing  Liu Jianfeng  Zhong Xue  Chen Zhiwen
Affiliation:Jilin Normal University, Institute of Eco-environmental Sciences, Siping Jilin 136000
Abstract:The best hormone ratio, training plantlet and transplant technology were studied to meet the requirements of large-scale production using three kinds of African violet (Saintpaulia ionantha ) of different leaf-types. Different concentrations and types of growth hormone on callus induction, adventitious bud germination, plantlets rooting, and different transplanting methods were investigated to optimize the factory production procedures. The results showed the best culture media of leaf callus induction were MS+6-BA 0.5 mg/L +NAA 0.3 mg/L and MS+6-BA 0.5 mg/L +NAA 0.5 mg/L. After four weeks cultivation, callus induction rate reached to 100%, and buds occurred on almost every callus. After subculture on the medium MS+6-BA 0.5 mg/L +NAA 0.3 mg/L, about 30 buds could be observed on one callus. There were no obvious differences in callus and bud induction in different cultivars. The proper culture medium for rooting culture was 1/2MS+0.2 mg/L NAA for varieties A and C, but 1/2MS+0.5 mg/L IBA for B variety. Vermiculite was the optimum medium for test-tube plantlet after transplant, and 1/4 MS (large elements and trace element) should be used as foliar fertilizer, and the survive rate of the root regeneration plant was over 90%. After transferred to humus, above 95% of plantlet could survive. After three months of cultivation, the African violet burst into blossom. Three kinds of African violet of different leaf-types tissue culture propagation technology system were successfully established in the study.
Keywords:regeneration systemzz
本文献已被 维普 万方数据 等数据库收录!
点击此处可从《中国农学通报》浏览原始摘要信息
点击此处可从《中国农学通报》下载全文
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