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基于亲和纯化的辣根过氧化物酶新方法。

A new approach for affinity-based purification of horseradish peroxidase.

机构信息

Molecular Biology and Genetics Department, Faculty of Science and Literature, Mus Alparslan University, Mus, Turkey.

Department of Medical Services and Techniques, Vocational School of Health Services, Agri Ibrahim Cecen University, Agri, Turkey.

出版信息

Biotechnol Appl Biochem. 2021 Feb;68(1):102-113. doi: 10.1002/bab.1899. Epub 2020 Apr 14.

Abstract

We have developed efficient procedure for isolation of horseradish peroxidase (HRP) using aminobenzohydrazide-based affinity chromatography. Sepharose 4B-bounded aminobenzohydrazides are suitable for long-term use and large-scale purification. In this study, 26 aminobenzohydrazide derivatives were synthesized, characterized and defined as new HRP inhibitors. In addition, detailed inhibition effects of these molecules on HRP enzyme were investigated. Affinity matrix was formed by bonding aminobenzohydrazides, which exhibited inhibitory activity to sepharose-4B-l-tyrosine. HRP was isolated from crude homogenate in single step and purification factors were recorded as 1,151-fold (recovery of 8.5%) with 4-amino 3-bromo benzohydrazide and as 166.16-fold (recovery of 16.67 %) with 3-amino 4-chloro benzohydrazide.

摘要

我们开发了一种使用基于氨基苯肼的亲和层析法高效分离辣根过氧化物酶(HRP)的方法。Sepharose 4B 结合的氨基苯肼适用于长期使用和大规模纯化。在这项研究中,合成了 26 种氨基苯肼衍生物,并对其进行了表征,将其定义为新的 HRP 抑制剂。此外,还详细研究了这些分子对 HRP 酶的抑制作用。亲和基质是通过结合具有抑制活性的氨基苯肼形成的,该基质与 sepharose-4B-l-酪氨酸结合。HRP 从粗匀浆中一步分离得到,用 4-氨基-3-溴苯肼进行纯化,得率为 8.5%,纯化倍数为 1151 倍;用 3-氨基-4-氯苯肼进行纯化,得率为 16.67%,纯化倍数为 166.16 倍。

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