Computer-Aided Molecular Modifications for Enhanced Activity and Thermal Stability of <sc>d</sc>-Allulose 3-Epimerase

D-Allulose 3-epimerase (DAE) can convert D-fructose into D-allulose, but its lower activity and poor thermal stability restrict its application in industrial production. This study utilized a semi-rational design and specific site mutations to enhance the enzyme activity and thermal stability of a DAE from Clostridium scindens ATCC 35704 (Csc-DAE) at the same time. Notably, the activities of six mutants (V22I, A25V, Q46I, C212N, G165A, and G267D) and the orderly superimposed double-point mutants were increased by 1.08-1.31 and 1.28-1.64 times that of the wild type (553.7 U/mg), respectively. In addition, A25V/C212N showed good thermal stability, and its optimum temperature (T (opt)) was 65 degrees C and half-life (t (1/2)) was 3.997 h at 60 degrees C, which increased by 5 degrees C and 5.76 times, respectively. The conversion ratio reached 30.62 and 31.22% at 65 and 70 degrees C, respectively, and the structural changes of the mutants were analyzed using molecular docking. These studies provide a beneficial mutation for industrial applications.