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一种通过β-葡萄糖醛酸酶的产生来检测大肠杆菌的快速荧光法。

A rapid fluorogenic method for the detection of Escherichia coli by the production of beta-glucuronidase.

作者信息

Sarhan H R, Foster H A

机构信息

Department of Biological Sciences, University of Salford, UK.

出版信息

J Appl Bacteriol. 1991 May;70(5):394-400. doi: 10.1111/j.1365-2672.1991.tb02955.x.

Abstract

A medium containing the fluorogenic substrate 4-methylumbelliferyl-beta-D-glucuronide was developed for the isolation and identification of Escherichia coli within 7.5 h and was based on the detection of beta-glucuronidase. Optimum conditions for the rapid development of fluorescent colonies were determined. The optimum temperature was 41.5 degrees C. Development of fluorescence was delayed when carbohydrates were incorporated into the medium. Water samples were used to evaluate the medium by surface plating and membrane filtration. The frequency of false-negative results was 6.1% and false-positives were 3.7% for freshwater samples. The false-positive organisms were identified as Klebsiella spp. and Shigella sonnei. The potential applications of the medium are discussed.

摘要

开发了一种含有荧光底物4-甲基伞形酮基-β-D-葡萄糖醛酸苷的培养基,用于在7.5小时内分离和鉴定大肠杆菌,该培养基基于β-葡萄糖醛酸酶的检测。确定了快速形成荧光菌落的最佳条件。最佳温度为41.5摄氏度。当培养基中加入碳水化合物时,荧光的形成会延迟。通过表面接种和平板过滤,用水样对该培养基进行评估。淡水样品的假阴性结果发生率为6.1%,假阳性为3.7%。假阳性菌被鉴定为克雷伯菌属和宋内志贺菌。讨论了该培养基的潜在应用。

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