Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10869921 | FEBS Letters | 2015 | 7 Pages |
Abstract
The glycoside hydrolase family (GH) 130 is composed of inverting phosphorylases that catalyze reversible phosphorolysis of β-d-mannosides. Here we report a glycoside hydrolase as a new member of GH130. Dfer_3176 from Dyadobacter fermentans showed no synthetic activity using α-d-mannose 1-phosphate but it released α-d-mannose from β-1,2-mannooligosaccharides with an inversion of the anomeric configuration, indicating that Dfer_3176 is a β-1,2-mannosidase. Mutational analysis indicated that two glutamic acid residues are critical for the hydrolysis of β-1,2-mannotriose. The two residues are not conserved among GH130 phosphorylases and are predicted to assist the nucleophilic attack of a water molecule in the hydrolysis of the β-d-mannosidic bond.
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Authors
Takanori Nihira, Kazuhiro Chiku, Erika Suzuki, Mamoru Nishimoto, Shinya Fushinobu, Motomitsu Kitaoka, Ken'ichi Ohtsubo, Hiroyuki Nakai,