College of Chemistry and Material Science, Shandong Agricultural University, Taian, 271018, Shandong, China.
Analyst. 2013 May 21;138(10):3026-31. doi: 10.1039/c3an00026e.
The presence of Escherichia coli (E. coli) in food and drinking water is a chronic problem worldwide. Protecting food against bacterial contamination and rapid diagnosis of infection require simple and rapid assays for detection of bacterial pathogens, including E. coli O157:H7. Here we report a rapid and novel colorimetric method for detecting E. coli O157:H7. This colorimetric method is based on the catalytic oxidation of the peroxidase substrate 3,3,5,5-tetramethylbenzidine by hydrogen peroxide using 4-mercaptophenylboronic acid-functioned Au@Pt nanoparticles adsorbed on the surface of E. coli O157:H7. The assay showed excellent sensitivity both with the naked eye and based on absorbance measurements. The absorbance at 652 nm was proportional to the concentration of E. coli O157:H7 ranging from 7 to 6 × 10(6) cfu mL(-1) with a limit of detection of 7 cfu mL(-1). The total detection time was less than 40 min.
食品和饮用水中存在大肠杆菌(E. coli)是一个全球性的长期问题。防止食物受到细菌污染和快速诊断感染需要简单快速的检测方法来检测细菌病原体,包括大肠杆菌 O157:H7。在这里,我们报告了一种快速新颖的比色法来检测大肠杆菌 O157:H7。这种比色法基于 4-巯基苯硼酸功能化的 Au@Pt 纳米粒子在大肠杆菌 O157:H7 表面吸附后,用过氧化氢催化过氧化酶底物 3,3,5,5-四甲基联苯胺的氧化。该测定法具有出色的灵敏度,无论是肉眼观察还是基于吸光度测量均如此。在 652nm 处的吸光度与大肠杆菌 O157:H7 的浓度成正比,浓度范围为 7 到 6×10(6)cfu mL(-1),检测限为 7 cfu mL(-1)。总检测时间少于 40 分钟。