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Journal of Southern Medical University ; (12): 904-908, 2014.
Article in Chinese | WPRIM | ID: wpr-249335

ABSTRACT

<p><b>OBJECTIVE</b>To construct enterohemorrhagic Escherichia coli (EHEC) O157: H7 ppk gene deletion strains and study its biological characteristics.</p><p><b>METHODS</b>The gene fragment of kanamycin resistance was amplified using a pair of homologous arm primers whose 5' and 3' ends were homologous with ppk gene and kanamycin resistance gene, respectively. EHEC O157: H7 EDL933w competent strains were prepared and transformed via electroporation with the amplification products. The ppk gene was replaced by kanamycin resistance gene using pKD46-mediated Red recombination system. The recombinant strain was confirmed by PCR and sequencing, and its morphology, growth ability and adhesion were assessed using Gram staining, OD600 value and Giemsa staining.</p><p><b>RESULTS AND CONCLUSION</b>We established a ppk-deleted EHEC O157:H7 EDL933w strain with kanamycin resistance and compared the biological characteristics of the wild-type and mutant strains, which may facilitate further study of the regulatory mechanism of ppk gene.</p>


Subject(s)
DNA Primers , Escherichia coli O157 , Genetics , Escherichia coli Proteins , Genetics , Gene Deletion , Phosphotransferases (Alcohol Group Acceptor) , Genetics , Polymerase Chain Reaction
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