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来自链球菌属和肠球菌属的活性组成型L-吡咯烷酮基肽酶的测定。

Measurement of active constitutive L-pyrrolidonyl-peptidase from the genera Streptococcus and Enterococcus.

作者信息

Panosian K J, Edberg S C

机构信息

Clinical Microbiology Laboratory, Yale-New Haven Hospital, CT.

出版信息

Med Microbiol Immunol. 1988;177(6):317-21. doi: 10.1007/BF02389903.

Abstract

In the family Streptococceae the ability to measure L-pyrrolidonyl-peptidase is limited to Lancefield group D Enterococcus and group A Streptococcus pyogenes. A number of methods exist to assay this enzyme. All measure pyrrolidonyl-peptidase by the ability of the bacterium to cleave L-pyrrolidonyl-beta-naphthylamide to form free beta-naphthylamine and L-pyrrolidone-carboxylic acid. Free beta-naphthylamine is then reacted with N,N-dimethylamino-cinnamaldehyde to form a red color complex. These methods are generally expensive and require a 2-4 h incubation period before results are available. A method, which employs the substrate dried on paper discs and can be easily made, is described herein. It is simple to perform, inexpensive, rapid, and has a long storage life. The results of this constitutive method are equivalent to those obtained using a commercial system.

摘要

在链球菌科中,测量L-吡咯烷酮基肽酶的能力仅限于兰斯菲尔德D组肠球菌和A组化脓性链球菌。有多种方法可用于检测这种酶。所有方法都是通过细菌裂解L-吡咯烷酮基-β-萘酰胺以形成游离的β-萘胺和L-吡咯烷酮羧酸的能力来测量吡咯烷酮基肽酶。然后使游离的β-萘胺与N,N-二甲基氨基肉桂醛反应形成红色复合物。这些方法通常成本高昂,并且在获得结果之前需要2-4小时的孵育期。本文描述了一种使用干燥在纸盘上的底物且易于制备的方法。该方法操作简单、成本低廉、快速,并且具有较长的储存寿命。这种简易方法的结果与使用商业系统获得的结果相当。

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