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凝结芽孢杆菌NL01 L-阿拉伯糖异构酶的理性设计及其F279I变体在D-塔格糖生产中的应用

Rational Design of Bacillus coagulans NL01 l-Arabinose Isomerase and Use of Its F279I Variant in d-Tagatose Production.

作者信息

Zheng Zhaojuan, Mei Wending, Xia Meijuan, He Qin, Ouyang Jia

机构信息

Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources , Nanjing 210037, People's Republic of China.

College of Chemical Engineering, Nanjing Forestry University , Nanjing 210037, People's Republic of China.

出版信息

J Agric Food Chem. 2017 Jun 14;65(23):4715-4721. doi: 10.1021/acs.jafc.7b01709. Epub 2017 May 30.

Abstract

d-Tagatose is a prospective functional sweetener that can be produced by l-arabinose isomerase (AI) from d-galactose. To improve the activity of AI toward d-galactose, the AI of Bacillus coagulans was rationally designed on the basis of molecular modeling and docking. After alanine scanning and site-saturation mutagenesis, variant F279I that exhibited improved activity toward d-galactose was obtained. The optimal temperature and pH of F279I were determined to be 50 °C and 8.0, respectively. This variant possessed 1.4-fold catalytic efficiency compared with the wild-type (WT) enzyme. The recombinant Escherichia coli overexpressing F279I also showed obvious advantages over the WT in biotransformation. Under optimal conditions, 67.5 and 88.4 g L d-tagatose could be produced from 150 and 250 g L d-galactose, respectively, in 15 h. The biocatalyst constructed in this study presents a promising alternative for large-scale d-tagatose production.

摘要

d-塔格糖是一种潜在的功能性甜味剂,可由d-半乳糖通过l-阿拉伯糖异构酶(AI)生产。为了提高AI对d-半乳糖的活性,基于分子建模和对接对凝结芽孢杆菌的AI进行了合理设计。经过丙氨酸扫描和位点饱和诱变,获得了对d-半乳糖活性提高的变体F279I。F279I的最适温度和pH分别确定为50℃和8.0。与野生型(WT)酶相比,该变体的催化效率提高了1.4倍。过表达F279I的重组大肠杆菌在生物转化方面也比WT表现出明显优势。在最佳条件下,15 h内分别由150 g/L和250 g/L的d-半乳糖可生产67.5 g/L和88.4 g/L的d-塔格糖。本研究构建的生物催化剂为大规模生产d-塔格糖提供了一种有前景的替代方案。

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