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Updated: Oct 17, 2025

Unraveling Entropic Rate Acceleration Induced by Solvent Dynamics in Membrane Enzymes
Published on: January 16, 2016
Conditional dependence of enzyme cascade reaction efficiency on the inter-enzyme distance
Peng Lin1, Huyen Dinh1, Eiji Nakata1
1Institute of Advanced Energy, Kyoto University, Uji, Kyoto 611-0011, Japan. t-morii@iae.kyoto-u.ac.jp.
Abstract:
A dual-enzyme cascade, xylitol dehydrogenase and xylulose kinase, derived from the xylose metabolic pathway, was constructed on a three-dimensional DNA scaffold which exhibited a dynamic shape transition from an open state to a closed hexagonal prism. Evaluation of the cascade reaction efficiencies in the open and closed states revealed little to no inter-enzyme distance dependence, presumably due to the far larger catalytic constant of the downstream enzyme. The inter-enzyme distance was not the dominant factor for cascade efficiency when the kinetic parameters of the cascade enzymes were imbalanced with the highly efficient downstream enzyme.
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