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Electrochemical measurement of catalase activity of Eschelida coli with use of H_2O_2 selective sol-gel film-modified electrode

机译:使用H_2O_2选择性溶胶 - 凝胶膜改性电极进行Eschelida Coli过氧化氢酶活性的电化学测量

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The catalase activity of Escherichia coli (E coli) was detected by using H2O2-selective sol-gel film modified platinum electrode. This sol-gel film is composed of three kinds of organosilanes and two biopolymers (i.e., chitosan and bovine serum albumin). This protein/polysaccharide/hybrid sol-gel membrane showed an excellent permselectivity to H2O2, based on a size exclusive mechanism. The steady-state anodic current obtained in the presence of 0.1 mM H2O2 was diminished by the addition of E. coli samples, due to the catalase activity of E. coli. The time-dependent decrease in current (I/t) was dependent on the E. coli density in the range from 106 to 107 CFU (colony forming units). Although the sensitivity is not sufficient, this electrochemical method may be applicable to discriminate calatase-positive and catalase-negative bacteria within 30 min.
机译:通过使用H 2 O 2选择性溶胶 - 凝胶膜改性铂电极检测大肠杆菌(E Coli)的过氧化酶活性。该溶胶 - 凝胶膜由三种有机硅烷和两个生物聚合物(即壳聚糖和牛血清白蛋白)组成。该蛋白质/多糖/杂化溶胶 - 凝胶膜基于尺寸专用机制显示出对H 2 O 2的优异偏移率。由于大肠杆菌的过氧化氢酶活性,通过添加大肠杆菌样品,在0.1mm H 2 O 2存在下获得的稳态阳极电流。电流(I / T)的时间依赖性降低依赖于106至107 CFU(菌落形成单元)的大肠杆菌密度。虽然灵敏度不足以,但这种电化学方法可以适用于在30分钟内区分消失酶阳性和过氧化酶阴性细菌。

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