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副结核分枝杆菌hsp65基因的克隆及序列分析
引用本文:徐凤宇,胡玉庆,曾范利,姜秀云,何昭阳. 副结核分枝杆菌hsp65基因的克隆及序列分析[J]. 吉林农业大学学报, 2009, 31(2)
作者姓名:徐凤宇  胡玉庆  曾范利  姜秀云  何昭阳
作者单位:吉林农业大学动物科技学院,长春,130118;吉林农业大学生命科学学院,长春,130118
基金项目:国家自然科学基金,吉林农业大学青年启动基金 
摘    要:以副结核分枝杆菌C-2株基因组DNA为模板,以hsp65基因特异性引物进行PCR扩增,获得了1 626 bp的DNA片段.通过T-A克隆技术,将PCR产物克隆至pGEM-T载体.经鉴定,成功地构建出了重组质粒pGEM-T-hsp65.序列分析结果表明:该序列与GenBank中副结核分枝杆菌K~10株的同源性为99.2%.

关 键 词:副结核分枝杆菌  hsp65基因  克隆  序列分析

Cloning and Sequence Analysis of Mycobacterium paratuberculosis hsp65 gene
XU Feng-yu,HU Yu-qing,ZENG Fan-li,JIANG Xiu-yun,HE Zhao-yang. Cloning and Sequence Analysis of Mycobacterium paratuberculosis hsp65 gene[J]. Journal of Jilin Agricultural University, 2009, 31(2)
Authors:XU Feng-yu  HU Yu-qing  ZENG Fan-li  JIANG Xiu-yun  HE Zhao-yang
Affiliation:XU Feng-yu1,HU Yu-qing1,ZENG Fan-li1,JIANG Xiu-yun2,HE Zhaoyang11.College of Animal Science , Technology,Jilin Agricultural University,Changchun 130118,China,2.College of Life Science
Abstract:The genomic DNA was extracted from Mycobacterium paratuberculosis(MP) strain C-2.The secreted protein hsp65 gene was amplified with a pair of specific primers using polymerase chain reaction(PCR).PCR product was anapproximate 1 626 bp DNA segment.The clone vector pGEM-T-hsp65 was constructed successfully by the PCR product that was cloned into pGEM-T vector using T-A clone technique, and the recombinant clone was identified by using complementation test,plasmid size test,restrictional enzyme assay,plasmid P...
Keywords:Mycobacterium paratuberculosis  hsp65 gene  cloning  sequence analysis  
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