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大肠杆菌表达人幽门螺杆菌尿素酶B亚单位跨膜区成份
引用本文:毛旭虎,鲁东水,郭红,吴超,王缚鲲,邹全明. 大肠杆菌表达人幽门螺杆菌尿素酶B亚单位跨膜区成份[J]. 免疫学杂志, 2001, 17(2): 94-96
作者姓名:毛旭虎  鲁东水  郭红  吴超  王缚鲲  邹全明
作者单位:第三军医大学临床微生物学教研室,
基金项目:国家“九五”重点攻关课题!(96 - 90 1- 0 1- 5 4),军队“九五”医药卫生科研基金!(98D0 44 )资助项目
摘    要:目的 重组表达人幽门螺杆菌尿素酶B亚单位跨膜区成份。方法 采用DNA重组技术将尿素酶B亚单位3’端732bp基因片段克隆至pET11C载体上,转化宿主菌BL21(DE3)E.coli,IPTG诱导,SDS-PAGE及Western-blot分析表达情况。结果 成功构建了含UreB0.7kb片段的重组质粒pET-UreB0.7,并表达了具有免疫反应性的分子量约28000u的重组蛋白,表达率为19.8%。结论 重组的尿素酶B亚单位跨膜区成份为研究其相关生物学特性奠定了重要基础。亦可作为Hp疫苗的成分用于Hp感染的预防和治疗。

关 键 词:幽门螺杆菌 大肠杆菌 尿素酶B亚单位 基因重组 跨膜区成份 DNA
文章编号:1000-8861(2001)02-0094-03
修稿时间:2000-11-27

Recombination and expression of a component of urease B subunit transmembrane protein of helicobacter pylori
MAO Xu-hu,LU Dong-shui,GUO Hong,WU Chao,WANG Fu-kun,ZOU Quan-ming. Recombination and expression of a component of urease B subunit transmembrane protein of helicobacter pylori[J]. Immunological Journal, 2001, 17(2): 94-96
Authors:MAO Xu-hu  LU Dong-shui  GUO Hong  WU Chao  WANG Fu-kun  ZOU Quan-ming
Abstract:Objective To recombine and express a component of urease B subunit transmembrane protein of helicobacter pylori. Methods A 732 bp gene fragment of urease B subunit of helicobacter pylori was cloned into pET11C and transformed into BL21(DE3)E.coli. The positive clone was induced with IPTG. The expression of target protein was analysed by SDS-PAGE and Western blot. Results It is successful to construct the recombinant plasmid pET-UreB0.7 containing urease B subunit 0.7 kb gene fragment. A protein (MW≈28 000 u) with immunoreactivity, was expressed by 19.8% in BL21(DE3)E.coli induced with IPTG. Conclusions The recombinant component of urease B subunit transmembrane protein may play a role in the research of its biological function and might be used as the vaccine against helicobacter pylori.
Keywords:helicobacter pylori  B subunit of urease  transmembrane protein  DNA recombination
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