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首页> 外文期刊>Journal of biomedical materials research, Part A >Immobilization of urease by laser techniques: synthesis and application to urea biosensors.
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Immobilization of urease by laser techniques: synthesis and application to urea biosensors.

机译:通过激光技术固定尿素酶:合成及其在尿素生物传感器中的应用。

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摘要

Urease thin films have been immobilized using matrix-assisted pulsed laser evaporation for biosensor applications in clinical diagnostics. The targets exposed to laser radiation were made of frozen composites that had been manufactured by dissolving urease in distilled water. An UV KrF* (lambda = 248 nm, tauFWHM congruent with 30 ns, nu = 10 Hz) excimer source was used for the multipulse laser irradiation of the targets that were cooled down to solidification using Peltier elements. The incident laser fluence was set at 0.4 J/cm2. The surface morphology and chemical bonding states of the laser immobilized urease thin films were investigated by atomic force microscopy and Fourier transform infrared spectroscopy. The enzymatic activity and kinetics of the immobilized urease were assayed by the Worthington method, which monitors urea hydrolysis by coupling ammonia production to a glutamate dehydrogenase reaction. Decreased absorbance was found at 340 nm and correlated with the enzymatic activity of urease.
机译:尿素酶薄膜已使用基质辅助脉冲激光蒸发固定化,用于生物传感器在临床诊断中的应用。暴露于激光辐射的靶材是由冷冻复合材料制成的,该复合材料是通过将脲酶溶解在蒸馏水中制成的。使用紫外线KrF *(λ= 248 nm,tauFWHM与30 ns,nu = 10 Hz一致)受激准分子源对目标进行多脉冲激光辐照,并使用Peltier元件将其冷却至凝固。入射激光通量设定为0.4J / cm 2。通过原子力显微镜和傅里叶变换红外光谱研究了激光固定的脲酶薄膜的表面形貌和化学键合状态。固定化脲酶的酶促活性和动力学通过沃辛顿方法进行了测定,该方法通过将氨的产生与谷氨酸脱氢酶反应偶联来监测尿素的水解。在340nm处发现吸光度降低,并且与脲酶的酶活性相关。

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