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Updated: Aug 16, 2025

Unraveling Entropic Rate Acceleration Induced by Solvent Dynamics in Membrane Enzymes
Published on: January 16, 2016
Kinetic Salt Effect on Base-Catalyzed Isomerization of d-Glucose into d-Fructose
Matthias Fischer1, Peter Drabo1, Lutz Burow1
1Institute for Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 2, 52074, Aachen, Germany.
Abstract:
Isomerization of d-glucose (Glc) into d-fructose (Fru) is of great importance for food sector as well as for valorization of lignocellulosic biomass. Soluble and solid bases exhibit high catalytic activity for the isomerization. Here, we report a salt effect on the base-catalyzed aqueous-phase Glc-Fru isomerization. Addition of soluble salts (Na2 SO4 , NaNO3 , K2 SO4 , and NaCl) results in an increased apparent reaction rate (factors of 1.5 to 6). The salt effect was observed both in the presence of soluble base NaOH at constant pH value and solid bases MgO, Li3 PO4 , and Mg-Al hydrotalcite. Apparent activation energy and UV absorption spectra were not significantly influenced by addition of salts. Potentiometric titration showed that the acidity constants of the saccharides increase in the presence of electrolytes. Since the rate of the isomerization depends on the thermodynamic acidity constant of Glc, the isomerization is accelerated by the presence of electrolytes.
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