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作 者:冯书章[1] 许崇波[1] 黄培堂[1] 刘子[1] 张喻虹 刘晓明[1] 李丰生 孟锐奇[1] 姚湘燕[1] 朱平[1]
机构地区:[1]解放军农牧大学军事兽医研究所
出 处:《中国兽医学报》1997年第2期112-115,共4页Chinese Journal of Veterinary Science
基 金:军队"八五"科学基金
摘 要:将构建的pBST2~6工程菌质粒用限制性内切酶BamHI/BglⅡ酶切,经琼脂糖凝胶电泳和电洗脱,回收147bp的目的ST1基因。随之将该基因分别重组到能有效表达K99菌毛抗原和LacZ酶的pGK99之K99基因BglⅡ位点和pUC18的BamHI位点中。通过ST1基因探针菌落原位杂交、特定酶切分析及DNA序列分析,筛选并鉴定出了理想重组子,从而构建出了能分别表达ST1融合基因产物的工程菌株pSK219和pXST1。The ST1gene of ETEC was amplified by PCR from agene engineering stra in pSLM004.The ST1gene fragment was inserted into the HincⅡsite of vector pUC18by blunt end ligation.The transformants were screened by clony hybridization in situ with α 32 PdATP labelling ST1gene probe,and identified by restriction endonuclease analysis and DNA sequencing.The recom binant plasmid pBST2 6was constructed,which contained ST1gene with BglⅡand Bam HI site (150bp).ST1gene fragments(147bp)obtained from pBST2 6by BglⅡand Bam HI digestion were re spectively inserted into the BglⅡsite of K99gene in pGK99,which could effectively express K99fim briae,and the Bam HI site of polycloning site of pUC18.In this way two kinds of recombinant plas mids,pSK219carrying ST1 K99fusion gene and pXST1carrying ST1 LacZ fusion gene,were suc cessfully constructed.The recombinant strains,pSK219and pXST1,were demonstrated to express ST1 K99fusion protein fimbriae and ST1 LacZ enzymatic fusion protein respectively.
分 类 号:Q78[生物学—分子生物学] S852.612[农业科学—基础兽医学]
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