Dual-Activity Mannosyltransferase Phosphorylases in Family 130 of Glycoside Hydrolases

We discovered that certain mannoside-active enzymes from family GH130 possess both glycoside phosphorylase (GP) and weak glycosyltransferase (GT) activities. This dual activity was observed only in glycoside phosphorylases acting on β-(1,2)- and β-(1,3)-mannosides, being absent in β-(1,4)-mannoside phosphorylases. We provide several three-dimensional (3D) structures of β-(1,2)-mannosyltransferase phosphorylases Uhgb_MS (identified from the human gut microbiome (subfamily GH130_4)) and Teth514_1788 (from <i>Thermoanaerobacter</i> sp. X514 (subfamily GH130_6)) and analyzed GT/GP partitioning among enzymes acting on d-mannosides. Structural analysis and mutagenesis of Uhgb_MS allowed us to show that loop L2 folding, as well as nucleotide and phosphate binding residues (P206, N211, R242) at the location of the common structural phosphate of αMan1P and GDP-Man, is an important structural element of bifunctionality in GH130.

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Journal
ACS Catalysis
Published
2025-12-24
DOI
https://doi.org/10.1021/acscatal.5c06782
Primary Topic
Enzyme Production and Characterization
Type
article
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article

Dual-Activity Mannosyltransferase Phosphorylases in Family 130 of Glycoside Hydrolases

Jérémy Esque, Julien Durand, Laurence Tarquis, Yannick Malbert et al.
ACS Catalysis
Enzyme Production and Characterization
article

Dual-Activity Mannosyltransferase Phosphorylases in Family 130 of Glycoside Hydrolases

Jérémy Esque, Julien Durand, Laurence Tarquis, Yannick Malbert, Gianluca Cioci, Régis Fauré, Simon Ladevèze, David Guieysse, Ao Li, Maxant Vivier, Élisabeth Laville, Gabrielle Potocki-Veronese
article en

Abstract

We discovered that certain mannoside-active enzymes from family GH130 possess both glycoside phosphorylase (GP) and weak glycosyltransferase (GT) activities. This dual activity was observed only in glycoside phosphorylases acting on β-(1,2)- and β-(1,3)-mannosides, being absent in β-(1,4)-mannoside phosphorylases. We provide several three-dimensional (3D) structures of β-(1,2)-mannosyltransferase phosphorylases Uhgb_MS (identified from the human gut microbiome (subfamily GH130_4)) and Teth514_1788 (from <i>Thermoanaerobacter</i> sp. X514 (subfamily GH130_6)) and analyzed GT/GP partitioning among enzymes acting on d-mannosides. Structural analysis and mutagenesis of Uhgb_MS allowed us to show that loop L2 folding, as well as nucleotide and phosphate binding residues (P206, N211, R242) at the location of the common structural phosphate of αMan1P and GDP-Man, is an important structural element of bifunctionality in GH130.

ACS CatalysisVol. 16(2)
Centre National de la Recherche Scientifique (FR), Université Fédérale de Toulouse Midi-Pyrénées (FR), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR), Saarbrücken Stadtwerke (Germany) (DE)
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Openalex Percentile: Top 32%
Enzyme Production and Characterization
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