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新疆绵羊种布鲁氏菌OMP25基因的分子克隆及核苷酸序列的测定
引用本文:柳建新,陈创夫,田晶华.新疆绵羊种布鲁氏菌OMP25基因的分子克隆及核苷酸序列的测定[J].中国兽医杂志,2005,41(11):6-8.
作者姓名:柳建新  陈创夫  田晶华
作者单位:石河子大学动物科技学院新疆地方与民族高发病重点实验室,新疆,石河子,832003
摘    要:根据GeneBank库上国际标准菌株绵羊种布鲁氏菌(63/290)的OMP25的基因序列设计引物,用聚合酶链式反应(PcR)技术从新疆绵羊种布鲁氏菌(80/019)基因组DNA中扩增出OMP25基因片段,TtDNA连接酶将其连接于PBS-T克隆载体质粒上,将重组质粒转化到受体菌DH10B中,蓝白斑筛选阳性菌落,结果成功克隆OMP25基因片段,进行核苷酸序列测定,测序结果分析表明:新疆绵羊菌株与国际标准菌株有明显差异。

关 键 词:新疆绵羊种布鲁氏菌  OMP25  克隆  核苷酸序列分析
文章编号:0529-6005(2005)11-0006-03
收稿时间:2004-11-04
修稿时间:2004年11月4日

Cloning and sequence analysis of the OMP25 gene of Brucella ovis in Xinjiang sheep
LIU Jian-xin,CHEN Chuang-fu,TIAN Jing-hua.Cloning and sequence analysis of the OMP25 gene of Brucella ovis in Xinjiang sheep[J].Chinese Journal of Veterinary Medicine,2005,41(11):6-8.
Authors:LIU Jian-xin  CHEN Chuang-fu  TIAN Jing-hua
Institution:Key Laboratory of Xinjiang Endemic and Ethnic Diseases, Animal Science Technology College, Shihezi University 832003
Abstract:Primers were devised according to putative omp25 gene sequence which was named as international standard strand 63/290, B. ovis. We took Xinjiang local B. ovis 80/019 as template, amplified gene fragment by PCR, ligated the fragment with PBS-T by T4 DNA ligase, transformed recombinant plasmid to E. coli DH10B by heat shock. The transformants were screened on ampicillin/Xgal-IPTG, on plate. Result- successfully cloned OMP25 gene fragment . Analysis of OMP25 gene sequence revealed that it was obviously different in OMP25 gene sequence of Xinjiang local B. ovis and that of international standard strain.
Keywords:Xinjiang Brucella ovis  OMP25  gene cloning
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