China National Center for Food Safety Risk Assessment, Key Laboratory of Food Safety Risk Assessment, Ministry of Health, Beijing 100021, PR China.
Biosens Bioelectron. 2013 Nov 15;49:99-104. doi: 10.1016/j.bios.2013.05.005. Epub 2013 May 9.
Regulatory restrictions on antibiotic residues in dairy products have resulted in the illegal addition of β-lactamase to lower antibiotic levels in milk in China. Here we demonstrate a fast, sensitive and convenient method based on enzyme thermistor (ET) for the surveillance of β-lactamase in milk. A fixed amount of penicillin G, which is a specific substrate of β-lactamase, was incubated with the milk sample, and an aliquot of the mixture was directly injected into the ET system to give a temperature change corresponding to the remained penicillin G. The amount of β-lactamase present in sample was deduced by the penicillin G consumed during incubation. This method was successfully applied to quantify β-lactamase in milk with the linear range of 1.1-20 UmL(-1) and the detection limit of 1.1 UmL(-1). The recoveries ranged from 93% to 105%, with relative standard deviations (RSDs) below 8%. The stability of the column equipped in ET was also studied, and only 5% decrease of activity was observed after 60 days of use. Compared with the conventional culture-based assay, the advantages of high throughput, timesaving and accurate quantification have made this method an ideal alternative for routine use.
由于对乳制品中抗生素残留的监管限制,在中国,β-内酰胺酶被非法添加到牛奶中,以降低牛奶中的抗生素水平。在这里,我们展示了一种基于酶热敏电阻(ET)的快速、敏感和方便的方法,用于监测牛奶中的β-内酰胺酶。将固定量的青霉素 G(β-内酰胺酶的特异性底物)与牛奶样品一起孵育,将混合物的一部分直接注入 ET 系统,以给出与剩余青霉素 G 相对应的温度变化。通过孵育过程中消耗的青霉素 G,可以推断出样品中存在的β-内酰胺酶的量。该方法成功地应用于定量检测牛奶中的β-内酰胺酶,线性范围为 1.1-20 UmL(-1),检测限为 1.1 UmL(-1)。回收率在 93%至 105%之间,相对标准偏差(RSD)低于 8%。还研究了 ET 中配备的柱子的稳定性,在使用 60 天后,仅观察到活性下降 5%。与传统的基于培养的测定方法相比,该方法具有高通量、省时和准确定量的优点,使其成为常规使用的理想替代方法。