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基于多功能锰核苷酸模拟漆酶纳米酶的有机污染物降解及利用智能手机可视化检测肾上腺素

Multifunctional Manganese-Nucleotide Laccase-Mimicking Nanozyme for Degradation of Organic Pollutants and Visual Assay of Epinephrine via Smartphone.

机构信息

Key Laboratory of Analytical Chemistry for Life Science of Shaanxi Province, Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an710119China.

出版信息

Anal Chem. 2024 Mar 19;96(11):4736-4744. doi: 10.1021/acs.analchem.4c00815. Epub 2024 Mar 11.

Abstract

As a natural green catalyst, laccase has extensive application in the fields of environmental monitoring and pollutant degradation. However, susceptibility to environmental influences and poor reusability seriously hinder its application. To address these concerns, for the first time, manganese ion replaced copper ion as the active center to coordinate with guanosine monophosphate (GMP) for synthesizing mimic laccase with high catalytic activity. Compared with natural laccase, the laccase-like nanozyme (Mn-GMPNS) demonstrated superior thermal stability, acid-base resistance, salt tolerance, reusability, and substrate universality. Benefiting from the high catalytic activity of Mn-GMPNS, epinephrine, a significant neurotransmitter and hormone associated with numerous diseases, was visually detected within 10 min and a portable assay by smartphone. More encouragingly, Mn-GMPNS can efficiently degrade dye pollutants, achieving a decolorization rate over 70% within 30 min. Thus, the coordination between manganese ion and nucleotide demonstrated the potential in rational design of nanozymes with high catalytic activity, low cost, good stability, and good biocompatibility.

摘要

作为一种天然绿色催化剂,漆酶在环境监测和污染物降解等领域有广泛的应用。但其易受环境影响和重复利用率低的问题严重限制了其应用。为了解决这些问题,我们首次以锰离子取代铜离子作为活性中心,与鸟苷单磷酸(GMP)配位合成具有高催化活性的模拟漆酶。与天然漆酶相比,漆酶样纳米酶(Mn-GMPNS)具有更好的热稳定性、酸碱稳定性、耐盐性、可重复使用性和底物通用性。得益于 Mn-GMPNS 的高催化活性,我们在 10 分钟内实现了对重要神经递质和激素肾上腺素的可视化检测,并通过智能手机实现了便携检测。更令人鼓舞的是,Mn-GMPNS 能够有效地降解染料污染物,在 30 分钟内实现了超过 70%的脱色率。因此,锰离子与核苷酸的配位为设计具有高催化活性、低成本、良好稳定性和良好生物相容性的纳米酶提供了新的思路。

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