首页> 外文期刊>Infection and immunity >Molecular cloning and expression in Escherichia coli K-12 of the gene for a hemagglutinin from Vibrio cholerae.
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Molecular cloning and expression in Escherichia coli K-12 of the gene for a hemagglutinin from Vibrio cholerae.

机译:霍乱弧菌血凝素基因的分子克隆和在大肠杆菌K-12中的表达。

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摘要

Using antiserum to the purified soluble hemagglutinin we isolated an Escherichia coli K-12 clone expressing the gene for a hemagglutinin from Vibrio cholerae 569B. The plasmid present in this clone was designated pPM471. By deletion analysis with both specific restriction endonucleases and Bal 31 nuclease, we localized the gene, to a 0.72-kilobase region of DNA, implying a molecular weight of less than 27,000 for the protein. Analysis in E. coli K-12 minicells of plasmids containing the cloned gene and deletion derivatives of these plasmids identified a protein of 24,000 daltons correlating with hemagglutinating activity. Using the cloned gene as a probe, we demonstrated the presence of homologous DNA in a variety of V. cholerae strains including both biotypes. Furthermore, by screening gene banks in E. coli K-12 of V. cholerae El Tor O17, we isolated several El Tor clones containing this region of DNA and also expressing hemagglutinating activity.
机译:使用针对纯化的可溶性血凝素的抗血清,我们分离了表达来自霍乱弧菌569B的血凝素基因的大肠杆菌K-12克隆。该克隆中存在的质粒命名为pPM471。通过使用特异性限制性核酸内切酶和Bal 31核酸酶的缺失分析,我们将该基因定位到DNA的0.72碱基碱基区域,这意味着该蛋白质的分子量小于27,000。含有克隆基因和这些质粒的缺失衍生物的质粒在大肠杆菌K-12小细胞中的分析鉴定出24,000道尔顿的蛋白与血凝活性相关。使用克隆的基因作为探针,我们证明了在包括两种生物型在内的多种霍乱弧菌菌株中同源DNA的存在。此外,通过在霍乱弧菌El Tor O17的大肠杆菌K-12中筛选基因库,我们分离了几个包含此DNA区域并表达血凝活性的El Tor克隆。

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