Rutinosidase from
<i>Aspergillus niger</i>
: crystal structure and insight into the enzymatic activity
作者:Petr Pachl、Jana Kapešová、Jiří Brynda、Lada Biedermannová、Helena Pelantová、Pavla Bojarová、Vladimír Křen、Pavlína Řezáčová、Michael Kotik
DOI:10.1111/febs.15208
日期:2020.8
three‐dimensional structure of a rutinosidase determined at 1.27‐Å resolution. The rutinosidase from Aspergillus niger K2 (An Rut), a member of glycoside hydrolase family GH‐5, subfamily 23, was heterologously produced in Pichia pastoris . The X‐ray structure of An Rut is represented by a distorted (β/α)8 barrel fold with its closest structural homologue being an exo‐β‐(1,3)‐glucanase from Candida albicans
Rutinosidases(α-升-rhamnosyl-β- d葡糖苷酶)催化糖苷配基之间的糖苷键的裂解的二糖芸香糖(α-升-rhamnopyranosyl-(1→6)-β- d -glucopyranose)特定的类黄酮的糖苷,如芦丁(槲皮素3- O-芦丁苷)。微生物芦丁糖苷酶是芦丁分解代谢途径的一部分,使微生物能够利用芦丁和相关的植物酚类糖苷。在这里,我们报告了以1.27-Å分辨率测定的芸香糖苷酶的第一个三维结构。从rutinosidase黑曲霉K2(一种车辙),糖苷水解酶家族GH-5,亚家族23的构件,在被异源生产巴斯德毕赤酵母。An Rut的X射线结构以扭曲的(β/α)8桶折叠表示,其最接近的结构同源物是来自白色念珠菌(Ca Exg)的exo- β-(1,3)-葡聚糖酶。催化部位位于与Ca Exg惊人的结构相似性的深袋中。但是,已发现An Rut活性位点的入口与Ca Exg的入口不同–