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用于检测细菌培养物中志贺毒素2的无细胞翻译检测法的验证

Validation of a cell-free translation assay for detecting shiga toxin 2 in bacterial culture.

作者信息

He Xiaohua, Quiñones Beatriz, Carter John Mark, Mandrell Robert E

机构信息

US Department of Agriculture, Western Regional Research Center, Agricultural Research Service, Albany, California 94710, USA.

出版信息

J Agric Food Chem. 2009 Jun 10;57(11):5084-8. doi: 10.1021/jf9002285.

Abstract

A cell-free translation (CFT) assay for detecting Shiga toxin (Stx) at different levels of purity has been validated. The limits of detection for pure Stx2 (PStx2) and partially pure Stx2 (PPStx2) in water reached 20 and 3.5 pg/microL, respectively, without the artificial process of proteolytic activation and reduction of the pro-toxin. The specific detection of Stx2 was confirmed by a neutralization test using Stx2-specific mouse monoclonal antibody. This assay can be used for differentiation of Stx-producing Escherichia coli from non-Stx-producing E. coli. Four E. coli O157:H7 strains genotypically different for Stx were tested. The translational inhibition of Stx-producing E. coli was significantly higher than that of non-Stx-producing E. coli when bacterial culture supernatants were used for the analysis. Inhibition occurred even with supernatants diluted 1000-fold. The thermal stability of Stx2 was studied using the CFT assay, and significant differences were observed among three Stx2 preparations heated at 70 degrees C for 60 min. It was concluded that the CFT assay is a rapid, specific, and sensitive method for detecting Stx2 activity.

摘要

一种用于检测不同纯度志贺毒素(Stx)的无细胞翻译(CFT)分析方法已得到验证。在无需对毒素原进行蛋白水解激活和还原这一人工处理的情况下,水中纯Stx2(PStx2)和部分纯化的Stx2(PPStx2)的检测限分别达到20和3.5 pg/微升。使用Stx2特异性小鼠单克隆抗体通过中和试验证实了对Stx2的特异性检测。该分析方法可用于区分产Stx大肠杆菌和非产Stx大肠杆菌。对4株在Stx基因分型上不同的大肠杆菌O157:H7菌株进行了测试。当使用细菌培养上清液进行分析时,产Stx大肠杆菌的翻译抑制作用明显高于非产Stx大肠杆菌。即使上清液稀释1000倍也会出现抑制作用。使用CFT分析方法研究了Stx2的热稳定性,在70℃加热60分钟的三种Stx2制剂之间观察到显著差异。得出的结论是,CFT分析方法是一种检测Stx2活性的快速、特异且灵敏的方法。

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