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A Novel Method to Prepare PolyGMA and its Application to Immobilization of β-Galactosidase

机译:一种制备多面容的新方法及其在β-半乳糖苷酶固定中的应用

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The reactive, macroporous and massive epoxy group containing polyGMA was synthesized simultaneously with methanol aqueous solution and nano-calcium carbonate as porogen by bulk copolymerization. After the polymer was smashed, particles with diameters in the range of 0.30 to 0.45 mm were taken as the carrier and the scanning electron microscopy (SEM) micrographs were done to characterize its surface structure. Under the optimum conditions, β-galactosidase was immobilized on the supporter obtained above and the enzyme activity bound per gram drier carrier could attained up to 77.33%, which was much higher than that bound on the carrier prepared by only using methanol aqueous solution as porogen. The conclusion obtained indicated that the ployGMA prepared concurrently with liquid and solid porogen was more suitable to immobilize enzyme because of the much more porous surface structure obtained.
机译:通过散装共聚合与甲醇水溶液和纳米碳酸钙同时合成反应性,大孔和大规模环氧基团。在粉碎聚合物之后,将具有0.30至0.45mm的直径的颗粒作为载体,并进行扫描电子显微镜(SEM)显微照片以表征其表面结构。在最佳条件下,将β-半乳糖酶固定在上述载体上,每克干燥载体结合的酶活性可达77.33%,其远高于仅使用甲醇水溶液作为孔剂制备的载体上结合的酶活性。所获得的结论表明,由于获得的多孔表面结构,与液体和固孔原制备的植物和固体致孔剂同时制备的植物更适合于固定酶。

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