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Data‐driven enzyme immobilisation: a case study using DNA to immobilise galactose oxidase

机译:数据驱动酶免除:使用DNA固定半乳糖氧化酶的案例研究

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摘要

Biocatalysis has the potential to enable green chemistry. New methods of enzyme immobilisation will be required to improve enzyme stability, product purification, and compatibility of different enzymes in the same reaction conditions. Deoxyribonucleic acid (DNA) stands out among supramolecular scaffolds, as simple Watson–Crick base-pairing rules can be used to rationally design a unique nanoscale environment around each individual enzyme in a cascade. Enhancements of enzyme activity and stability on DNA nanostructures have previously been reported, but never in the context of industrially relevant chemical syntheses or reaction conditions. Here, the authors show DNA can enhance the activity and stability of a galactose oxidase mutant, which could be used in a cascade to produce bioplastics from lignin. The enzyme was enhanced in the cell-free extract, which to their knowledge has not been shown before for any enzymes on DNA. This is significant because crude biocatalytic reactions are vastly more cost-effective. This opens the door to further work on multienzyme cascades by tuning the properties of individual enzymes.
机译:生物催化具有使绿色化学的潜力。酶固定化的新方法将被要求提高酶的稳定性,产品的纯化,和不同酶的相容性在相同的反应条件。脱氧核糖核酸(DNA)突出超分子支架中,作为简单的Watson-Crick碱基配对规则可用于合理设计围绕在级联每个单独的酶的独特的纳米级环境。在DNA纳米结构酶的活性和稳定性的增强先前已经报道,但从未在工业有关的化学合成或反应条件的情况下。在此,作者证明DNA能够提高半乳糖氧化酶突变体,其可以在一个级联从木质素被用于生产生物塑料的活性和稳定性。将酶在无细胞提取物,其对他们的知识还未用在DNA酶的任何前所示增强。因为原油生物催化反应有很大的更具成本效益这是显著。这通过调整各种酶的特性敞开了大门上多酶级联进一步的工作。

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