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鼠疫耶尔森氏菌LcrV基因的克隆及序列分析
引用本文:王忠泽,荫俊,王威,白洁,侯晓军,宋伟,张松乐.鼠疫耶尔森氏菌LcrV基因的克隆及序列分析[J].生物技术通讯,2001,12(1):18-19.
作者姓名:王忠泽  荫俊  王威  白洁  侯晓军  宋伟  张松乐
作者单位:1. 北京微生物流行病研究所
2. 白求恩医科大学
摘    要:为了研究鼠疫耶尔森氏菌(Y.pestis)保护性抗原V蛋白,从基因库中查得Y.pestis LcrV基因DNA序列,针对序列设计合成了一对PCR扩增引物,以本所保存的Y.pestis菌种为模板进行基因扩增,结果获得长约980bp的DNA片段。将扩增产物回收纯化,克隆至pGEM-T载体,构建重组载体pGEN-T/ypV,经过PCR,酶切鉴定,并对pGEM-T/ypV中的V基因片段进行测序,分析测序结果与己知序列相同,表明获得了LcrV基因。

关 键 词:鼠疫耶尔森氏菌  基因克隆  测序  LcrV基因  基因克隆
修稿时间:2000年8月4日

Cloning and sequencing of LcrVgene of Yersinia pestis
WANG ZhongZe,YIN Jun,WANG Wei,BAI Jie,HO U XiaoJun,SOUNG Wei,ZHANG Songle.Cloning and sequencing of LcrVgene of Yersinia pestis[J].Letters in Biotechnology,2001,12(1):18-19.
Authors:WANG ZhongZe  YIN Jun  WANG Wei  BAI Jie  HO U XiaoJun  SOUNG Wei  ZHANG Songle
Institution:WANG Zhong?Ze 1,YIN Jun 1,WANG Wei 1,BAI Jie 2,HOU Xiao?Jun 1,SOUNG Wei 1,ZHANG Song?Le 1
Abstract:To study the protective antigen V protein of Yersinia pestis, a pair of primers for PCR were designed according to published DNA sequence of Y. pestis LcrV gene and synthesized. A DNA fragment about 980 bp length was gotten through PCR amplification. After recycled and purified, the DNA fragment was ligated with pGEM?T Vector and recombined vector pGEM?T/ypV was constructed. The pGEM?T/ypV plasmid was then identified by PCR, enzyme digestion and sequencing, and the sequence was the same as the published sequence.
Keywords:Yersinia pestis  gene clone  sequencing
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