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酶在沸石咪唑酯骨架材料中的封装:可控共沉淀法与仿生矿化法的比较

Enzyme encapsulation in zeolitic imidazolate frameworks: a comparison between controlled co-precipitation and biomimetic mineralisation.

作者信息

Liang Kang, Coghlan Campbell J, Bell Stephen G, Doonan Christian, Falcaro Paolo

机构信息

CSIRO Manufacturing Flagship, Private Bag 10, Clayton South, Victoria 3169, Australia.

出版信息

Chem Commun (Camb). 2016 Jan 11;52(3):473-6. doi: 10.1039/c5cc07577g. Epub 2015 Nov 9.

DOI:10.1039/c5cc07577g
PMID:26548587
Abstract

Recent studies have demonstrated that metal-organic frameworks can be employed as protective coatings for enzymes. Two efficient strategies have been reported for the synthesis of such composite materials: biomimetic mineralisation and controlled co-precipitation using polyvinylpyrrolidone. We assessed the relative efficacy of each approach by comparing the thermal stability of encapsulated urease. The resulting data shows that over a range of temperatures biomimetic mineralisation offers superior protection than the co-precipitation method.

摘要

最近的研究表明,金属有机框架可作为酶的保护涂层。已报道了两种合成此类复合材料的有效策略:仿生矿化和使用聚乙烯吡咯烷酮的可控共沉淀。我们通过比较包封脲酶的热稳定性来评估每种方法的相对效果。所得数据表明,在一定温度范围内,仿生矿化提供的保护比共沉淀法更好。

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