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Microelectrode Control of Surface-Bound Enzymatic Activity

机译:表面结合酶活性的微电极控制

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Microelectrodes have been used to control the microscopically local reaction environment of surface-bound alcohol dehydrogenase (ADH). A surface comprised of agarose beads coated with immobilized ADH was prepared on a microscope slide and exhibited maximum activity toward the oxidation of ethanol, in the presence of nicotinamide adenine dinucleotide (NAD↑(+)), at a pH of 9.0. Microelectrode control of activity was achieved by submerging the slide in a solution of pH 6.0, well below the optimum value, and generating hydroxide at the microelectrode tip through the reduction of oxygen or water. An alkaline "sphere of influence" was set up around the microelectrode tip that, when positioned in close proximity to the enzyme surface, created a favorable reaction environment. The increased enzymatic activity was monitored by observing fluorescence of the reduced cofactor, NADH, using a fluorescence microscope equipped with an imaging camera. The fluorescent sphere diameter was characterized as a function of time, potential, and solution buffer strength. Optimum spatial resolution for enzymatic control was 7-12 μm.
机译:微电极已用于控制表面结合的醇脱氢酶(ADH)的微观局部反应环境。在显微镜载玻片上制备由涂有固定化ADH的琼脂糖珠组成的表面,在烟酰胺腺嘌呤二核苷酸(NAD↑(+))的存在下,在pH值为9.0时,对乙醇的氧化表现出最大活性。通过将载玻片浸没在远低于最佳值的pH 6.0溶液中,并通过还原氧气或水在微电极尖端生成氢氧化物,从而实现对微电极的活性控制。在微电极尖端周围建立了一个碱性的“影响范围”,当其紧邻酶表面放置时,会创造一个良好的反应环境。通过使用配备有成像相机的荧光显微镜观察还原的辅因子NADH的荧光来监测增加的酶活性。荧光球直径表征为时间,电势和溶液缓冲液强度的函数。酶促控制的最佳空间分辨率为7-12μm。

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