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[氧化酶活性快速测定方法参数的实验原理]

[Experimental rationale for the parameters of a rapid method for oxidase activity determination].

作者信息

Butorina N N

出版信息

Gig Sanit. 2010 Sep-Oct(5):48-52.

Abstract

Experimental rationale is provided for the parameters of a rapid (1-2-min) test to concurrently determine the oxidase activity of all bacteria grown on the membrane filter after water filtration. Oxidase reagents that are the aqueous solutions of tetramethyl-p-phenylenediamine dihydrochloride and demethyl-p-phenylenediamine dihydrochloride have been first ascertained to exert no effect on the viability and enzymatic activity of bacteria after one-hour contact. An algorithm has been improved for the rapid oxidase activity test: the allowable time for bacteria to contact oxidase reagents and procedures for minimizing the effect on bacterial biochemical activity following the contact. An accelerated method based on lactose medium with tergitol 7 and Endo agar has been devised to determine coliform bacteria, by applying the rapid oxidase test: the time of a final response is 18-24 hours. The method has been included into GOST 52426-2005.

摘要

为一种快速(1 - 2分钟)检测方法的参数提供了实验依据,该方法用于同时测定水过滤后膜滤器上生长的所有细菌的氧化酶活性。已首先确定,作为盐酸四甲基对苯二胺和盐酸脱甲基对苯二胺水溶液的氧化酶试剂在接触一小时后对细菌的活力和酶活性没有影响。改进了快速氧化酶活性检测的算法:确定了细菌与氧化酶试剂接触的允许时间以及将接触后对细菌生化活性的影响降至最低的程序。通过应用快速氧化酶检测,设计了一种基于含有特吉托尔7的乳糖培养基和远藤琼脂的加速方法来测定大肠菌群:最终反应时间为18 - 24小时。该方法已纳入GOST 52426 - 2005标准。

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