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在酰胺水解酶超家族的外围:来自嗜碱芽孢杆菌的Bh0493催化D-半乳糖醛酸异构化为D-塔罗糖醛酸。

At the periphery of the amidohydrolase superfamily: Bh0493 from Bacillus halodurans catalyzes the isomerization of D-galacturonate to D-tagaturonate.

作者信息

Nguyen Tinh T, Brown Shoshana, Fedorov Alexander A, Fedorov Elena V, Babbitt Patricia C, Almo Steven C, Raushel Frank M

机构信息

Department of Chemistry, P.O. Box 30012, Texas A&M University, College Station, Texas 77842-3012, USA.

出版信息

Biochemistry. 2008 Jan 29;47(4):1194-206. doi: 10.1021/bi7017738. Epub 2008 Jan 3.

Abstract

The amidohydrolase superfamily is a functionally diverse set of enzymes that catalyzes predominantly hydrolysis reactions involving sugars, nucleic acids, amino acids, and organophosphate esters. One of the most divergent members of this superfamily, uronate isomerase from Escherichia coli, catalyzes the isomerization of d-glucuronate to d-fructuronate and d-galacturonate to d-tagaturonate and is the only uronate isomerase in this organism. A gene encoding a putative uronate isomerase in Bacillus halodurans (Bh0705) was identified based on sequence similarity to uronate isomerases from other organisms. Kinetic evidence indicates that Bh0705 is relatively specific for the isomerization of d-glucuronate to d-fructuronate, confirming this functional assignment. Despite a low sequence identity to all other characterized uronate isomerases, phylogenetic and network-based analysis suggests that a second gene in this organism, Bh0493, is also a uronate isomerase, although it is an outlier in the group, with <20% sequence identity to any other characterized uronate isomerase from another species. The elucidation of the X-ray structure at a resolution of 2.0 A confirms that Bh0493 is a member of the amidohydrolase superfamily with conserved residues common to other members of the uronate isomerase family. Functional characterization of this protein shows that unlike Bh0705, Bh0493 can utilize both d-glucuronate and d-galacturonate as substrates. In B. halodurans, Bh0705 is found in an operon for the metabolism of d-glucuronate, whereas Bh0493 is in an operon for the metabolism of d-galacturonate. These results provide the first identification of a uronate isomerase that operates in a pathway distinct from that for d-glucuronate. While most organisms that contain this pathway have only one gene for a uronate isomerase, sequence analysis and operon context show that five other organisms also appear to have two genes and one organism appears to have three genes for this activity.

摘要

酰胺水解酶超家族是一组功能多样的酶,主要催化涉及糖类、核酸、氨基酸和有机磷酸酯的水解反应。该超家族中差异最大的成员之一,来自大肠杆菌的糖醛酸异构酶,催化D-葡萄糖醛酸向D-果糖醛酸以及D-半乳糖醛酸向D-塔罗糖醛酸的异构化反应,并且是该生物体中唯一的糖醛酸异构酶。基于与其他生物体糖醛酸异构酶的序列相似性,在嗜碱芽孢杆菌中鉴定出一个编码假定糖醛酸异构酶的基因(Bh0705)。动力学证据表明,Bh0705对D-葡萄糖醛酸向D-果糖醛酸的异构化反应具有相对特异性,证实了这一功能归属。尽管与所有其他已表征的糖醛酸异构酶的序列同一性较低,但基于系统发育和网络的分析表明,该生物体中的另一个基因Bh0493也是一种糖醛酸异构酶,尽管它在该组中是一个异常值,与来自其他物种的任何其他已表征的糖醛酸异构酶的序列同一性<20%。分辨率为2.0 Å的X射线结构解析证实,Bh0493是酰胺水解酶超家族的成员,具有糖醛酸异构酶家族其他成员共有的保守残基。对该蛋白的功能表征表明,与Bh0705不同,Bh0493可以利用D-葡萄糖醛酸和D-半乳糖醛酸作为底物。在嗜碱芽孢杆菌中,Bh0705存在于一个用于D-葡萄糖醛酸代谢的操纵子中,而Bh0493存在于一个用于D-半乳糖醛酸代谢的操纵子中。这些结果首次鉴定出一种在与D-葡萄糖醛酸不同的途径中起作用的糖醛酸异构酶。虽然大多数含有该途径的生物体只有一个糖醛酸异构酶基因,但序列分析和操纵子背景表明,另外五个生物体似乎也有两个基因,还有一个生物体似乎有三个该活性的基因。

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