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Use of urea filter paper disc to detect urease activity in Enterobacteriaceae by multipoint replication techniques.

机译:使用尿素滤纸盘通过多点复制技术检测肠杆菌科细菌中的尿素酶活性。

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摘要

A new method of detecting urease activity in Enterobacteriaceae was developed. An 8.5 cm filter paper disc impregnated with 20% urea and 0.5% bromocresol purple was placed on the surface of a glucose fermentation plate after inoculation with a multipoint replicator and overnight incubation. This method was compared with the commercially prepared Mast urea agar (Multipoint) and Fuscoe's Urea Plate Medium. A total of 240 routine isolates of Enterobacteriaceae were tested for urease activity using the three methods. Sixty five isolates were positive by the three methods while 33 isolates gave differing results. The urea disc method was more sensitive for detecting urease activity in isolates of Klebsiella species, Morganella morganii, and Yersinia enterocolitica. It also overcame the problem associated with the other two media of diffusion of alkali end products through the medium.
机译:开发了一种检测肠杆菌科细菌脲酶活性的新方法。用多点复制器接种并过夜孵育后,将浸渍有20%尿素和0.5%溴甲酚紫的8.5 cm滤纸圆片放在葡萄糖发酵板的表面。将该方法与市售的肥大的尿素琼脂(Multipoint)和Fuscoe的尿素平板培养基进行了比较。使用这三种方法测试了共240株常规肠杆菌科细菌的脲酶活性。三种方法对65株分离株呈阳性反应,而33株分离株得到不同的结果。尿素盘法对于检测克雷伯菌,摩根氏菌和小肠结肠炎耶尔森氏菌的分离物中的尿素酶活性更为敏感。它还克服了与碱最终产物通过该介质扩散的其他两种介质有关的问题。

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  • 作者

    Winter, D B; McDermott, S N;

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  • 年度 1990
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  • 原文格式 PDF
  • 正文语种 en
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