苯甲醛裂解酶活性的直接分光光度法测定。

Biotechnology Research International Pub Date : 2011-01-01 Epub Date: 2011-07-14 DOI:10.4061/2011/478925
Dessy Natalia, Christina Kohlmann, Marion B Ansorge-Schumacher, Lasse Greiner
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引用次数: 3

摘要

荧光假单胞菌(Pseudomonas fluorescens Biovar I., BAL, EC 4.1.2.38)苯甲醛裂解酶是手性α-羟基酮有机合成的多功能催化剂。为了快速评估酶的活性,需要直接分光光度法测定。本文提出了一种新的基于紫外吸收的可靠且易于操作的检测方法。该方法是基于α-羟基酮(R)-2,2'-呋喃与2-呋喃醛的连接。通过方便的浓度工作范围,使与低浓度相关的实验最小化,促进了对产品直接监测的可靠分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Direct spectrophotometric assay for benzaldehyde lyase activity.

Direct spectrophotometric assay for benzaldehyde lyase activity.

Direct spectrophotometric assay for benzaldehyde lyase activity.

Direct spectrophotometric assay for benzaldehyde lyase activity.

Benzaldehyde lyase from Pseudomonas fluorescens Biovar I. (BAL, EC 4.1.2.38) is a versatile catalyst for the organic synthesis of chiral α-hydroxy ketones. To allow fast assessment of enzyme activity, a direct spectrophotometric assay is desirable. Here, a new robust and easy-to-handle assay based on UV absorption is presented. The assay developed is based on the ligation of the α-hydroxy ketone (R)-2,2'-furoin from 2-furaldehyde. A robust assay with direct monitoring of the product is facilitated with a convenient concentration working range minimising experimental associated with low concentrations.

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