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Semi-Continuous Flow Biocatalysis with Affinity Co-Immobilized Ketoreductase and Glucose Dehydrogenase

机译:具有亲和力共固定的酮还原酶和葡萄糖脱氢酶的半连续流体生物分析

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摘要

The co-immobilization of ketoreductase (KRED) and glucose dehydrogenase (GDH) on highly cross-linked agarose (sepharose) was studied. Immobilization of these two enzymes was performed via affinity interaction between His-tagged enzymes (six histidine residues on the N-terminus of the protein) and agarose matrix charged with nickel (Ni2+ ions). Immobilized enzymes were applied in a semicontinuous flow reactor to convert the model substrate; α-hydroxy ketone. A series of biotransformation reactions with a substrate conversion of >95% were performed. Immobilization reduced the requirement for cofactor (NADP+) and allowed the use of higher substrate concentration in comparison with free enzymes. The immobilized system was also tested on bulky ketones and a significant enhancement in comparison with free enzymes was achieved.
机译:研究了在高度交联的琼脂糖(Sepharose)上的酮还原酶(Kred)和葡萄糖脱氢酶(GDH)的共固化。通过其标记的酶(六个末端的六个末端的六个组氨酸残基在蛋白质的六个组氨酸残基)和用镍(Ni2 +离子)中的琼脂糖基质进行固定的固定化。将固定化酶施加在半连续流量反应器中以转换模型基材; α-羟基酮。进行含有> 95%的基材转化的一系列生物转化反应。固定化减少了辅因子(NADP +)的要求,并允许使用更高的底物浓度与游离酶相比。固定化的体系也在庞大的酮上测试,实现了与游离酶比较的显着增强。

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