首页 | 本学科首页   官方微博 | 高级检索  
     

柑桔炭疽菌果胶裂解酶pelB基因特异性引物的筛选
引用本文:谭萍,王勇,姜于兰. 柑桔炭疽菌果胶裂解酶pelB基因特异性引物的筛选[J]. 广东农业科学, 2012, 39(1): 130-131,135
作者姓名:谭萍  王勇  姜于兰
作者单位:贵州大学农学院
基金项目:贵州省农业攻关项目(黔科合NY字[2009]3006)
摘    要:以柑桔炭疽菌为主要研究对象,根据已知的炭疽菌果胶裂解酶pelB基因序列,运用GenBank及Primer Premier 5共设计6对引物,其中编号为PB1/PB2、Cg1A/Cg1b及Cg2a/Cg2b的引物可扩增出pelB基因片段,经同源性分析,全序列与GenBank中登录号为GU478342.1 pelB基因的的同源性高达98%,PB1/PB2、Cg1A/Cg1b对柑桔胶孢炭疽菌果胶裂解酶pelB基因有较高特异性。

关 键 词:胶孢炭疽菌  果胶裂解酶  特异性引物

Screening of pelB-specific primers for pectate lyase gene of Colletotrichum gloeosprioides
TAN Ping,WANG Yong,JIANG Yu-lan. Screening of pelB-specific primers for pectate lyase gene of Colletotrichum gloeosprioides[J]. Guangdong Agricultural Sciences, 2012, 39(1): 130-131,135
Authors:TAN Ping  WANG Yong  JIANG Yu-lan
Affiliation:(Agriculture College,Guizhou University,Guiyang 550025,China)
Abstract:Colletotrichum gloeosprioides was the main object in this study.Six pairs of primers according to the conservative sequence of the reported pelB gene were designed with GenBank and Primer Premier 5 and then the six pairs of primers were amplified by PCR.The result showed that the primers numbered PB1/PB2,Cg1A/Cg1b and Cg2a/Cg2b could be amplified pelB gene fragment.Comparing and analysising the sequencing result to the reported sequence showed that the amplified fragment of pelB gene was above 98% homology with GenBank the accessioned number GU478342.1.However,the three specific designed primers were not specific with other common pathogens.
Keywords:Colletotrichum gloeosprioides  pectate lyase  specific primers
本文献已被 CNKI 等数据库收录!
点击此处可从《广东农业科学》浏览原始摘要信息
点击此处可从《广东农业科学》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