Young S A, Tenover F C, Gootz T D, Gordon K P, Plorde J J
Antimicrob Agents Chemother. 1985 May;27(5):739-44. doi: 10.1128/AAC.27.5.739.
Two DNA probes were developed to screen for the genes encoding 3'-aminoglycoside phosphotransferase activity in gram-negative bacilli. The 3'-I phosphotransferase [APH(3')I] probe was subcloned from Tn903; the APH(3')II probe was subcloned from Tn5. Each probe proved to be specific for genes corresponding to its own APH(3') subclass and did not hybridize with DNA from other classes when tested at high stringency by either Southern hybridization or dot-blot hybridization methods. The APH(3')I probe hybridized to DNA obtained from organisms demonstrating APH(3')I activity as measured by the phosphocellulose paper binding assay (PPBA) as well as to DNA from organisms reported to have both APH(3')I and APH(3')II activity by PPBA. This probe did not hybridize to DNA from organisms showing only APH(3')II activity by PPBA. The APH(3')II probe demonstrated homology with DNA from organisms showing APH(3')II activity by PPBA but not with DNA from organisms showing APH(3')I activity or both APH(3')I and APH(3')II activity by PPBA. We conclude that organisms previously believed to contain both APH(3')I and APH(3')II genes based on PPBA contain in fact only the APH(3')I gene.
开发了两种DNA探针,用于筛选革兰氏阴性杆菌中编码3'-氨基糖苷磷酸转移酶活性的基因。3'-I磷酸转移酶[APH(3')I]探针是从Tn903亚克隆而来;APH(3')II探针是从Tn5亚克隆而来。通过Southern杂交或斑点印迹杂交方法在高严谨度下进行测试时,每种探针都被证明对与其自身APH(3')亚类相对应的基因具有特异性,并且不会与其他类别的DNA杂交。APH(3')I探针与通过磷酸纤维素纸结合测定法(PPBA)测量显示具有APH(3')I活性的生物体获得的DNA杂交,也与通过PPBA报告同时具有APH(3')I和APH(3')II活性的生物体的DNA杂交。该探针不会与通过PPBA仅显示APH(3')II活性的生物体的DNA杂交。APH(3')II探针与通过PPBA显示具有APH(3')II活性的生物体的DNA具有同源性,但与通过PPBA显示具有APH(3')I活性或同时具有APH(3')I和APH(3')II活性的生物体的DNA没有同源性。我们得出结论,以前基于PPBA被认为同时含有APH(3')I和APH(3')II基因的生物体实际上只含有APH(3')I基因。