Experiment-3 of the intestinal pancreatic chymotrypsin (20 U/mL) effects (with describing model parameter estimates on GH5-p4818Cel5_2A activity over a 5-h period after the intestinal pancreatic chymotrypsin buffer being mixed with the heat-treated enzyme preparation for incubation at the resulting mixture pH = 6.0–7.0 and chymotrypsin (20 U/mL) prior to further incubation for measuring cellulase activity with the carboxymethyl cellulose (CMC) substrate buffer in presence of dithiothreitol (DTT) (5 mM) and N2 gas purging for 15 min at 37 °C. (A) Plot of the inhibition kinetic relationship between the GH5-p4818Cel5_2A activity (v, mean nmol/mg protein•min) and incubation time (t, h) established according to the exponential response model as: , P < 0.0001 for all parameter estimates; , n = 84; and alternatively according to the linear response model established as: , P < 0.0001 for all the parameter estimates; , n = 84; (B) Plot of the inhibition kinetic relationship between the relative GH5-p4818Cel5_2A activity (v, mean % of the control group measured at Ic of 100.000 ± 2.455) at 0-min exposure to the chymotrypsin-20-U/mL incubation) and incubation time (t, h) established according to the exponential response model as: , P < 0.0001 for all the parameter estimates; , n = 84; and alternatively according to the linear response model established as: , P < 0.0001 for all parameter estimates; , n = 84; (C) the Eadie-Hofstee linear plot between the GH5-p4818Cel5_2A enzyme activity (v, mean nmol/mg protein•min) and the v/t ratio established as: , P < 00001 for all parameter estimates, , n = 72; and (D) the Eadie-Hofstee linear plot between the relative GH5-p4818Cel5_2A enzyme activity (v, mean % of the control group measured Ic of 100.000 ± 2.455) at 0-min exposure to the chymotrypsin-20-U/mL incubation) and the v/t ratio established as: , P < 0.0001 for all parameter estimates; n = 72.