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P(GMA-HEMA)/SiO2 Nanofilm Constructed Macroporous Monolith for Immobilization of Pseudomonas Fluorescens Lipase

机译:P(GMA-HEMA)/SIO2纳米膜构建了大孔巨石,用于固定荧光脂肪酶

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摘要

Monolithic macroporous composites constructed by poly (glycidyl methacrylate-2-hydroxyethyl methacrylate)/SiO2 nano-film (P(GMA-HEMA)/SiO2) were prepared and then used as the supports for immobilization of Pseudomonas fluorescens lipase (PFL). The as-prepared macroporous materials were characterized by scanning electron microscope (SEM), N2 adsorption-desorption experiments, Fourier transform infrared (FT-IR) spectroscopy and thermogravimetric (TG) analysis. The immobilization conditions and the properties of the immobilized PFL were investigated. The characterization results revealed that the macroporous SiO2 has a 3D continuous pass-through macropore structure, large pore volume and high specific surface area. After modification with P(GMA-HEMA) and the subsequent immobilization of PFL, the structural characteristics were preserved. Under the optimum conditions, the activity of the immobilized PFL reached to 3773 Ug~(-1) and enzyme activity recovery achieved to 232%. Compared with free lipase, the thermal and pH stabilities of the immobilized lipase were significantly enhanced, and it also exhibited an outstanding reusability.
机译:由聚(甲基丙烯酸甲酯-2-羟基乙基甲基丙烯酸甲酯)/SIO2纳米 - 纳米胶质细胞(P(GMA-HEMA)/SIO2)构建的单片大孔复合材料,然后用作固定假单胞菌荧光酶(PFL)(PFL)的支持。用扫描电子显微镜(SEM),N2吸附 - 吸附实验,傅立叶变换红外(FT-IR)光谱和热重仪(TG)分析来表征所需的大孔材料。研究了固定条件和固定PFL的特性。表征结果表明,大孔SIO2具有3D连续的大孔结构,较大的孔体积和高比表面积。用P(GMA-HEMA)修饰并随后固定PFL后,保留了结构特征。在最佳条件下,固定的PFL的活性达到3773 ug〜(-1),酶活性恢复达到232%。与游离脂肪酶相比,固定脂肪酶的热和pH稳定性显着增强,并且还具有出色的可重复性。

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