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Characterization of a β-Glucosidase from Fragaria × ananassa: Substrate Specificity, Catalytic Efficiency, and
Ibrahim Rabeeah1, Alberto Zavarise1, Alessandro Manghi1,2
1Research Group Phytochemistry and Biochemistry of Natural Compounds, Institute of Chemical, Environmental and Bioscience Engineering, Technische Universität Wien, 1060 Wien, Austria.
Abstract:
β-Glucosidases (βGLs) play important roles in plant secondary metabolism by hydrolyzing glycosylated compounds involved in defense, signaling, and the formation of bioactive and flavor-related metabolites. In this study, a β-glucosidase from Fragaria × ananassa (Fra-βGL; FxaC_10g48920.t1) was identified and biochemically characterized in comparison with a commercial β-glucosidase from Prunus dulcis (Pru-βGL). The Fra-βGL cDNA was cloned and heterologously expressed in Escherichia coli, and the recombinant protein was purified for biochemical characterization. Substrate screening demonstrated that Fra-βGL hydrolyzed the 7-O-glucosides of quercetin, kaempferol, and luteolin, whereas no detectable activity was observed toward the tested 3-O-glucosides, anthocyanin glucosides, arbutin, or phloridzin under the assay conditions. Kinetic analysis revealed higher catalytic efficiencies of Fra-βGL than Pru-βGL toward all four substrates examined. Fra-βGL showed its highest turnover rate and catalytic efficiency toward the synthetic substrate p-nitrophenyl-β-D-glucopyranoside (pNP-Glc), with a Kcat of 60.33 s-1 and a Kcat/Km of 10.18 mM-1·s-1. Among the naturally occurring flavonoid glucosides, Fra-βGL exhibited the highest catalytic efficiency toward quercetin 7-O-glucoside (4.14 mM-1·s-1), approximately fivefold higher than that of Pru-βGL (0.824 mM-1·s-1). Thermal stability analysis showed progressive loss of activity with increasing temperature, with Pru-βGL retaining greater residual activity than Fra-βGL at elevated temperatures. Molecular docking suggested structural features that may contribute to the observed preference of Fra-βGL for flavonoid 7-O-glucosides over the corresponding 3-O-glucosides. Collectively, these findings demonstrate the substrate selectivity and distinct catalytic properties of Fra-βGL and identify Fra-βGL as a candidate for further investigation in the context of flavonoid glycoside metabolism in strawberry.
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