Crystal structure of glycoside hydrolase family 31 α-xylosidase from a soil metagenome
Crystal structure of glycoside hydrolase family 31 α-xylosidase from a soil metagenome
复制标题
土壤宏基因组中糖苷水解酶家族 31 α-木糖苷酶的晶体结构
DOI:
10.1093/bbb/zbac058
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发表时间:
2022
期刊:
影响因子:
--
通讯作者:
Yaoi Katsuro
中科院分区:
文献类型:
--
作者:
Nakamichi Yusuke;Matsuzawa Tomohiko;Watanabe Masahiro;Yaoi Katsuro
MeXyl31, a member of glycoside hydrolase family 31 (GH31), is the α-xylosidase isolated from a soil metagenomic library. The enzyme degrades α-xylosyl substrate such as isoprimeverose, α-d-xylopyranosyl-(1→6)-glucopyranose. The crystal structure of MeXyl31 was determined at 1.80 Å resolution. MeXyl31 forms the tetrameric state. The complexed structure with a xylose in the −1 subsite (α-xylose binding site) shows that the enzyme strictly recognizes α-xylose. Structural comparison between MeXyl31 and its homologue,Aspergillus nigerα-xylosidase in GH31, gave insights into the positive subsite of MeXyl31. First, in the tetrameric enzyme, two monomers (a catalytic monomer and the adjacent monomer), are involved in substrate recognition. Second, the adjacent monomer composes a part of positive subsites in MeXyl31. Docking simulation and site-directed mutagenesis suggested that the Arg100 from the adjacent monomer is partially involved in the recognizing of a glucopyranose of isoprimeverose.