首页> 外文期刊>Journal of Clinical Microbiology >Enhancement of fluorescence development of end products by use of a fluorescence developer solution in a rapid and sensitive fluorescent spot test for specific detection of microbial beta-lactamases.
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Enhancement of fluorescence development of end products by use of a fluorescence developer solution in a rapid and sensitive fluorescent spot test for specific detection of microbial beta-lactamases.

机译:通过在快速而灵敏的荧光斑点测试中使用荧光显影剂溶液增强终产物的荧光显影,以特异性检测微生物β-内酰胺酶。

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摘要

A fluorescent spot test method for specific detection of microbial beta-lactamases as previously published (K. C. S. Chen, J. S. Knapp, and K. K. Holmes, J. Clin. Microbiol. 19:818-825, 1984) was improved by the use of a fluorescence developer solution. The fluorescence developer solution used in this study consisted of 0.78 M sodium tartrate buffer containing 12% formaldehyde at a final pH of 4.5. An addition of 1 volume of fluorescence developer solution to 5 volumes of ampicillin or cephalex substrate solution incubated with beta-lactamase-producing organisms, followed by heating the mixture at 45 degrees C for 10 min resulted in enhancement of fluorescence of the end products of beta-lactamase activity. This provides a more sensitive assay for microbial beta-lactamases and offers the potential for direct detection of beta-lactamases in clinical specimens.
机译:如前所述(KCS Chen,JS Knapp,和KK Holmes,J.Clin.Microbiol。19:818-825,1984),一种用于特异性检测微生物β-内酰胺酶的荧光斑点测试方法得到了改进。解。这项研究中使用的荧光显影剂溶液由0.78 M的酒石酸钠缓冲液组成,其中的最终pH为4.5,其中含有12%的甲醛。将1体积的荧光显影剂溶液添加到5体积与产生β-内酰胺酶的生物体一起孵育的氨苄青霉素或cephalex底物溶液中,然后将混合物在45摄氏度下加热10分钟,导致β终产物的荧光增强-内酰胺酶活性。这为微生物β-内酰胺酶提供了更灵敏的检测方法,并为直接检测临床标本中的β-内酰胺酶提供了潜力。

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