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大肠杆菌黏附素蛋白与热稳定肠毒素融合基因植物表达载体的构建
引用本文:孔庆军,任雪艳,李卓夫.大肠杆菌黏附素蛋白与热稳定肠毒素融合基因植物表达载体的构建[J].家畜生态,2005(4).
作者姓名:孔庆军  任雪艳  李卓夫
作者单位:新疆石河子大学生物工程学院 新疆石河子832003 (孔庆军,任雪艳),东北农业大学农学院 黑龙江哈尔滨150030(李卓夫)
基金项目:兵团博士基金项目(项目编号:兵博02)
摘    要:利用DNA重组技术,将编码大肠杆菌黏附素蛋白K 88ac与热稳定肠毒素ST II的融合基因的序列片段克隆到植物表达载体pB in48中,成功地构建了植物重组表达质粒pB in48-K 88-ST,并将其转化到农杆菌EHA 105中,为K 88ac-ST II基因的进一步研究奠定了基础。

关 键 词:菌毛抗原K88ac  大肠杆菌肠毒素  植物重组表达质粒  基因克隆

The Construction of Plant Expression Vector of the Fused Gene k88-STII
KONG Qing-jun.The Construction of Plant Expression Vector of the Fused Gene k88-STII[J].Ecology of Domestic Animal,2005(4).
Authors:KONG Qing-jun
Institution:KONG Qing-jun~
Abstract:The plant recombinant expression plasmod pBin-K88-ST had been successfully constructed by cloning the gene of K88-ST into the plant expression vector pBin438.The molecular biological technique such as double-enzyme-insertion was also used in this research.The plant binary expression vector of K88-ST was transformed into A grobacterium EHA 105.It provided a reliable basis for the further study on the Fused gene of antigen k88ac and STII of enteotoxigenic Escherichincoli.
Keywords:antigen K88ac  Enteotoxigenic Escherichia coli  STII plant recombination expression plasmid  gene cloning
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