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Purification of Alcohol Dehydrogenase from Saccharomyces cerevisiae Using Magnetic Dye-Ligand Affinity Nanostructures

机译:磁性染料-配体亲和纳米结构从酿酒酵母中纯化酒精脱氢酶

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摘要

Reactive Green 19 was covalently immobilized onto magnetic nanostructures for purification of alcohol dehydrogenase from Saccharomyces cerevisiae. The Reactive Green 19 immobilized magnetic nanostructures were characterized by Fourier transform infrared spectroscopy, electron spin resonance, atomic force microscope, and energy dispersive X-ray analysis. Particle size of nanostructures was found to be roughly 70 nm. Alcohol dehydrogenase adsorption experiments were investigated under different conditions in batch system (i.e., medium pH, alcohol dehydrogenase concentration, temperature, and ionic strength). Maximum alcohol dehydrogenase adsorption capacity was found to be 176.09 mg/g polymer while nonspecific alcohol dehydrogenase adsorption onto plain magnetic nanostructures was negligible (19.4 mg/g polymer). Alcohol dehydrogenase molecules were desorbed by using 1.0 M NaCl with 98.4 % recovery. Alcohol dehydrogenase from S. cerevisiae was purified 45.63-fold in single step with dye-immobilized magnetic nanostructures, and purity of alcohol dehydrogenase was shown by silver-stained sodium dodecyl sulfate-polyacrylamide gel electrophoresis.
机译:将反应性绿色19共价固定在磁性纳米结构上,以从酿酒酵母中纯化乙醇脱氢酶。通过傅立叶变换红外光谱,电子自旋共振,原子力显微镜和能量色散X射线分析对Reactive Green 19固定的磁性纳米结构进行了表征。发现纳米结构的粒度为约70nm。在分批系统的不同条件下(即中等pH值,酒精脱氢酶浓度,温度和离子强度)研究了酒精脱氢酶的吸附实验。发现最大的醇脱氢酶吸附容量为176.09 mg / g聚合物,而可将非特异性醇脱氢酶吸附至纯磁性纳米结构上的吸附微不足道(19.4 mg / g聚合物)。通过使用1.0 M NaCl解吸乙醇脱氢酶分子,回收率为98.4%。用染料固定的磁性纳米结构一步纯化纯化酿酒酵母中的乙醇脱氢酶45.63倍,并通过银染十二烷基硫酸钠-聚丙烯酰胺凝胶电泳显示醇脱氢酶的纯度。

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