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

rRNA基因ITS区序列分析在粘帚霉属生防菌株种级分类上的应用
引用本文:马桂珍,张拥华,李世东,谢丙炎.rRNA基因ITS区序列分析在粘帚霉属生防菌株种级分类上的应用[J].应用与环境生物学报,2007,13(5):704-707.
作者姓名:马桂珍  张拥华  李世东  谢丙炎
作者单位:1. 淮海工学院海洋学院,江苏连云港,222005;中国农科院植物保护研究所
2. 中国农科院植物保护研究所
3. 中国农科院蔬菜花卉研究所,北京,100081
基金项目:国家高技术研究发展计划(863计划)
摘    要:对分离自不同地域的粘帚霉属不同种类的生防菌株rRNA基因转录间区进行了克隆测序,用Clustal X软件进行自动排序,用Njplot程序构建系统进化树.供试26个粘帚霉菌株分在4个组,与传统形态分类结果一致,同一种类的不同来源的菌株差异不明显.研究表明,可以根据ITS区DNA序列差异对粘帚霉属进行种级分类,但不能用于区分种内不同地域的菌株之间的差别.图1表1参17

关 键 词:粘帚霉  rRNA基因转录间区  克隆  序列
收稿时间:2006-06-01
修稿时间:2006-10-13

Application of 5.8S rRNA ITS Sequence Analysis in Gliocladium Species Classification
MA Guizhen,ZHANG Yonghua,LI Shidong,XIE Bingyan.Application of 5.8S rRNA ITS Sequence Analysis in Gliocladium Species Classification[J].Chinese Journal of Applied and Environmental Biology,2007,13(5):704-707.
Authors:MA Guizhen  ZHANG Yonghua  LI Shidong  XIE Bingyan
Institution:1 Ocean College, Huaihai Institute of Technology, Lianyungang 22005, Jiangsu, China;2 Institute of Plant Protection, 3 Institute of Vegetable and Flower, Chinese Academy of Agricultural Sciences, Beijing 10008, China
Abstract:Classification of Gliocladium spp.was mostly done based on the methods of morphology and presented some difficulties.Molecular technique was used,and 26 Gliocladium isolates were investigated by 5.8S rDNA amplification with ITS1 and ITS4 as primers,sequencing and blast analysis.Results showed that the isolates tested were divided into 4 groups,the species of different groups were closely homologous and were different from control fungi.The phylogenetic tree also revealed that the same species isolates from different regions were not differ obviously and would be included in the same group.ITS sequence analysis result was identical to that of morphological classification of these fungi.It was concluded that the method of rDNA ITS sequence analysis was a powerful tool for the classification of Gliocladium at species level.Fig 1,Tab 1,Ref 17
Keywords:Gliocladium  ITS  clone  sequencing
本文献已被 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