Enhanced activity of enzymes encapsulated in spheres metal azolate framework-7 with defects.

IF 7.7 1区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY International Journal of Biological Macromolecules Pub Date : 2024-11-17 DOI:10.1016/j.ijbiomac.2024.137689
Cai Cheng, Xiaoliang Guo, Yu Feng, Jie Yu, Shi Huang, Liexiong Zhang, Yu Wu, Linna Shao, Xuehan Xu, Lingling Feng
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Abstract

Developing metal-organic frameworks (MOFs) with specific structures is critical for improving the activity of embedded enzymes, and defects may be one of the effective methods. Several methods have been demonstrated to be effective in creating defects in MOFs, including post-synthetic treatments, the use of acid as a modulator, and the use of ordinary or thermally sensitive linkers. However, these methods necessitate the utilization of additional substances. Metal azolate framework-7 (MAF-7) is a kind of MOF that was formed by the coordination of Zn2+ with 3-methyl-1,2,4-triazole (Hmtz). This paper presents a method for the preparation of defect MAF-7 by changing the sequence of reactants without the introduction of additional substances. The defects were characterized by a range of techniques, including scanning electron microscopy, transmission electron microscopy, Brunauer-Emmett-Teller, X-ray photoelectron spectroscopy, and powder X-ray diffraction. The activity of microcystinase A (MlrA) encapsulated in defective MAF-7 (CMlrA@DMAF-7) was found to be significantly increased in comparison to non-porous MAF-7 (NMAF-7), and was largely unaffected by alterations in synthesis conditions. It is also noteworthy that lysozyme (LZ) and horseradish peroxidase (HRP), which are commonly used in industry, also demonstrated enhanced activity when encapsulated in DMAF-7. It was therefore anticipated that modifying the sequence of reactant addition would be a straightforward and simple method of introducing defects into MAF-7, thereby improving enzyme utilization.

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增强封装在有缺陷的偶氮金属框架-7 中的酶的活性。
开发具有特定结构的金属有机框架(MOFs)对于提高嵌入酶的活性至关重要,而缺陷可能是有效的方法之一。有几种方法已被证明能有效地在 MOFs 中产生缺陷,包括后合成处理、使用酸作为调制剂以及使用普通或热敏连接体。不过,这些方法都需要使用额外的物质。金属偶氮框架-7(MAF-7)是一种由 Zn2+ 与 3-甲基-1,2,4-三唑(Hmtz)配位形成的 MOF。本文介绍了一种在不引入额外物质的情况下,通过改变反应物的顺序来制备缺陷 MAF-7 的方法。通过一系列技术,包括扫描电子显微镜、透射电子显微镜、布鲁瑙尔-艾美特-泰勒、X 射线光电子能谱和粉末 X 射线衍射,对缺陷进行了表征。研究发现,与无孔 MAF-7(NMAF-7)相比,封装在有缺陷 MAF-7 (CMlrA@DMAF-7)中的微囊藻毒素酶 A(MlrA)的活性显著提高,并且基本不受合成条件变化的影响。值得注意的是,工业中常用的溶菌酶(LZ)和辣根过氧化物酶(HRP)在被 DMAF-7 封装后也显示出更强的活性。因此,预计修改反应物的添加顺序将是在 MAF-7 中引入缺陷的一种简单直接的方法,从而提高酶的利用率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Journal of Biological Macromolecules
International Journal of Biological Macromolecules 生物-生化与分子生物学
CiteScore
13.70
自引率
9.80%
发文量
2728
审稿时长
64 days
期刊介绍: The International Journal of Biological Macromolecules is a well-established international journal dedicated to research on the chemical and biological aspects of natural macromolecules. Focusing on proteins, macromolecular carbohydrates, glycoproteins, proteoglycans, lignins, biological poly-acids, and nucleic acids, the journal presents the latest findings in molecular structure, properties, biological activities, interactions, modifications, and functional properties. Papers must offer new and novel insights, encompassing related model systems, structural conformational studies, theoretical developments, and analytical techniques. Each paper is required to primarily focus on at least one named biological macromolecule, reflected in the title, abstract, and text.
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