期刊文献+

人幽门螺杆菌热休克蛋白A亚单位的基因克隆及序列分析 被引量:2

Clone and sequence analysis of human Helicobacter pylori heat shock protein A gene
在线阅读 下载PDF
导出
摘要 目的获取人幽门螺杆菌 (helicobacter pylori,Hp)热休克蛋白 A基因 (hsp A )进行核苷酸序列分析。方法利用 PCR技术扩增 Hsp A的 DNA,并将其定向插入 Pin Point TMXa- 3载体中进行核苷酸序列分析。结果所克隆的 Hsp A DNA序列与 Gene Bank公布的序列有 15个碱基存在差异 ,同源 95 .8%。结论所克隆的 Hsp A基因可用于重组表达及相关研究。 ObjectiveTo obtain DNA of human Helicobacter pylori (Hp) heat shock protein A(hspA), and investigate the nucleotide sequence. MethodsThe HspA DNA was amplified by PCR from the chromosomal DNA of clinical isolated Helicobacter pylori and inserted into PinPoint TM Xa-3 Then the sequence was analysed. ResultsThe HspA gene's nucleotide homology was 95 8% as compared to that in Genebank. ConclusionA confirmed HspA gene has been obtained, thus a good foundation for recombination, expression and associated research laid. [
出处 《免疫学杂志》 CAS CSCD 北大核心 2001年第3期185-188,共4页 Immunological Journal
基金 国家"九五"重点攻关课题! (96 - 90 1- 0 1- 5 4) 全军"九五"医药卫生科研基金! (98D0 0 4)资助项目
关键词 幽门螺杆菌 热休克蛋白A 序列分析 亚单位 基因克隆 helicobacter pylori heat shock protein A sequence analysis
  • 相关文献

参考文献6

  • 1萨姆布鲁克J 金冬雁(译).分子克隆实验指南[M].北京:科学出版社,1992.55-56.
  • 2奥斯佰F 布伦特R 等.精编分子生物学实验指南[M].北京:科学出版社,1998.39.
  • 3奥斯伯 F,精编分子生物学实验指南,1998年,39页
  • 4范学工,幽门螺杆菌感染.基础与临床,1997年,33页
  • 5Wu L F,Res Microbiol,1992年,143卷,3期,347页
  • 6萨姆布鲁克 J,分子克隆实验指南,1992年

共引文献46

同被引文献20

  • 1D.R.马歇克 等.蛋白质纯化与鉴定实验指南[M].北京:科学出版社,1999.77-79.
  • 2颜子颖 王海林(译).精编分子生物学实验指南[M].北京:科学出版社,1999.480-487.
  • 3[1]Nakagawa I, Takahashi I, Kiyono H, et al. Oral immunization with the B subunit of the heat-labile enterotoxin of Escherichia coli induces early TH1 and late TH2 cytokine expression in Peyer's patches[J]. J Infect Dis, 1996, 173(6):1 428- 1 436.
  • 4[2]Truitt RL, Hanke C, Radke J, et al. Glycosphingolipids as novel targets for T-cell suppression by the B subunit of recombinant heat-labile enterotoxin [ J]. Infect Immun, 1998,66(4): 1 299 - 1 308.
  • 5[3]Yankelevich B, Soldatenkov VA, Hodgson J, et al. Differential induction of programmed cell death in CD8+ and CD4+ T cells by the B subunit of cholera toxin[J]. Cell Immunol, 1996, 168(2):229- 234.
  • 6[4]Li TK, Fox BS. Cholera toxin B subunit binding to an antigen-presenting cell directly co-stimulates cytokine production from a T cell clone[J]. Int Immunol, 1996, 8(12):1 849-1 856.
  • 7[5]Millar DG, Hirst TR, Snider DP. Escherichia coli heat-labile enterotoxin B subunit is a more potent mucosal adjuvant than its closely related homologue, the B subunit of cholera toxin[J]. Infect Immun, 2001, 69(5) :3 476- 3 482.
  • 8[6]Leece R , Hirst TR . Expression of the B subunit of Escherichia coli heat-labile enterotoxin in a marine Vibrio and in a mutant that is pleiotropically defective in the secretion of extracellular proteins[J]. J Gen Microbiol, 1992, 138 (4):719 - 724.
  • 9[8]Kozuka S, Yasuda Y, Isaka M, et al. Efficient extracellular production of recombinant Escherichia coli heat-labile enterotoxin B subunit by using the expression/secretion system of Bacillus brevis and its mucosal immunoadjuvanticity[J]. Vaccine, 2000, 18(17): 1 730 - 1 737.
  • 10[10]Tamura S, Asanuma H, Tomita T, et al. Escherichia coli heat-labile enterotoxin B subunits supplemented with a trace amount of the holotoxin as an adjuvant for nasal influenza vaccine[J].Vaccine. 1994, 12(12):1 083- 1 089.

引证文献2

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部