作者
Andreja Vujičić-Žagar, Tjaard Pijning, Slavko Kralj, Cesar A López, Wieger Eeuwema, Lubbert Dijkhuizen, Bauke W Dijkstra
发表日期
2010/12/14
期刊
Proceedings of the National Academy of Sciences
卷号
107
期号
50
页码范围
21406-21411
出版商
National Academy of Sciences
简介
Glucansucrases are large enzymes belonging to glycoside hydrolase family 70, which catalyze the cleavage of sucrose into fructose and glucose, with the concomitant transfer of the glucose residue to a growing α-glucan polymer. Among others, plaque-forming oral bacteria secrete these enzymes to produce α-glucans, which facilitate the adhesion of the bacteria to the tooth enamel. We determined the crystal structure of a fully active, 1,031-residue fragment encompassing the catalytic and C-terminal domains of GTF180 from Lactobacillus reuteri 180, both in the native state, and in complexes with sucrose and maltose. These structures show that the enzyme has an α-amylase-like (β/α)8-barrel catalytic domain that is circularly permuted compared to the catalytic domains of members of glycoside hydrolase families 13 and 77, which belong to the same GH-H superfamily. In contrast to previous suggestions, the …
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