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Probing traces of hydrogen peroxide by use of a biosensor based on mediator-free DNA and horseradish peroxidase immobilized on silver nanoparticles

机译:通过使用基于无介体DNA的生物传感器和辣根过氧化物酶固定在银纳米颗粒上的生物传感器探测痕量过氧化氢

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摘要

A new electrochemical biosensor for determination of hydrogen peroxide (H2O2) has been developed by immobilizing horseradish peroxidase (HRP) on silver colloids (nanosilver) and use of a DNA-functionalized interface. In the presence of the DNA and the nanosilver the immobilized HRP gives a pair of well-defined redox peaks with an electron-transfer rate constant of 3.27 +/- 0.91 s(-1) in pH 7.0 PBS. The presence of DNA also provides a biocompatible microenvironment for enzyme molecules, greatly amplifies the amount of HRP molecules immobilized on the electrode surface, and improves the sensitivity of the biosensor. Under optimum conditions the biosensor has electrocatalytic activity in the reduction of hydrogen peroxide with linear dependence on H2O2 concentration in the range 1.5 x 10(-6) to 2.0 x 10(-3) mol L-1; the detection limit is 5.0 x 10(-7) mol L-1 at a signaltonoise ratio of 3. The K-m(app) m value of HRP in the composite membrane was found to be 1.62 mmol L-1. These results suggest that the properties of the complex film, with its bioelectrochemical catalytic activity, could make it useful for development of bioelectronic devices and for investigation of protein electrochemistry at functional interfaces.
机译:通过将辣根过氧化物酶(HRP)固定在银胶体(nanosilver)上并使用DNA功能化的界面,已开发出一种用于测定过氧化氢(H2O2)的新型电化学生物传感器。在存在DNA和纳米银的情况下,固定的HRP在pH 7.0 PBS中产生一对明确定义的氧化还原峰,其电子传递速率常数为3.27 +/- 0.91 s(-1)。 DNA的存在还为酶分子提供了生物相容的微环境,极大地放大了固定在电极表面的HRP分子的数量,并提高了生物传感器的灵敏度。在最佳条件下,生物传感器对过氧化氢的还原具有电催化活性,对H2O2浓度的线性依赖性在1.5 x 10(-6)到2.0 x 10(-3)mol L-1之间;检测限为5.0 x 10(-7)mol L-1,信号音比为3。复合膜中HRP的K-m(app)m值为1.62 mmol L-1。这些结果表明,复合膜的特性及其生物电化学催化活性,使其可用于生物电子器件的开发和功能界面蛋白质电化学的研究。

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