首页 | 本学科首页   官方微博 | 高级检索  
     检索      

显齿蛇葡萄离体快繁体系的建立
引用本文:张霞,杨朝东,倪德江.显齿蛇葡萄离体快繁体系的建立[J].安徽农业科学,2011,39(17):10157-10159,10166.
作者姓名:张霞  杨朝东  倪德江
作者单位:长江大学园艺园林学院,湖北,荆州,434025;华中农业大学园艺林学学院,农业部亚热带农业资源与环境重点开放实验室,湖北,武汉,430070
基金项目:黑龙江自然科学基金项目(C200620)
摘    要:目的]利用组织培养的方法建立快速、高效的显齿蛇葡萄快速繁殖体系。方法]以显齿蛇葡萄带芽茎段为材料,研究了不同灭菌方法、培养基和激素组合对显齿蛇葡萄离体快繁的影响。结果]外植体采用75%乙醇浸泡20s+0.1%HgCl2处理8min+吐温-801-2滴灭菌效果较好;腋芽诱导适宜的培养基为B5+1.00mg/LBA+0.05mg/LNAA;增殖培养以MS/B5+1.50mg/LBA+0.05mg/LNAA为宜;生根以1/2MS+O.50mg/LIBA的培养基效果好。结论]建立了一个显齿蛇葡萄离体快繁的高频率发生体系,为其愈伤再生体系、遗传转化及无性系变异筛选奠定了技术基础。

关 键 词:显齿蛇葡萄  外植体  离体培养

Establishment of Rapid Propagation System in vitro of Ampelopsis grossedentata
ZHANG Xia et al.Establishment of Rapid Propagation System in vitro of Ampelopsis grossedentata[J].Journal of Anhui Agricultural Sciences,2011,39(17):10157-10159,10166.
Authors:ZHANG Xia
Institution:ZHANG Xia et al (College of Forestry,Northeast Forestry University,Harbin,Heilongjiang 150040)
Abstract:Objective] The ras promoters were cloned from genomic DNA of Auricuralia auricular so as to provide promoters for breeding better species by genetic technology.Method] PCR was used to clone promoters with the genomic DNA of A.auricular strain YBS-3 as template,and then the sequences of four ras promoters were obtained.The analysis of promoter sequences was made by three promoter analysis software:Promoter prediction,Place and TFSEARCH ver.1.3.Result] Four fragments contained core elements of promoter inc...
Keywords:Auricuralia auricular  ras promoter  Cloning  Sequence analysis  
本文献已被 CNKI 维普 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