The ability of ectoin, hydroxyectoin, glycoin (known as extremolytes), glutaraldehyde (GA) and methoxypoly(ethylene glycol) (MeOPEG) to produce formulations of alpha-chymotrypsin (alpha-CT) more active than the native enzyme in organic solvents, was tested. The activity in toluene of lyophilized alpha-CT when ectoin, MeOPEG (1:1, w/w) or GA (0.1%, w/v) were used was 10-, 46-, and 260-fold higher than in the absence of additives, respectively; furthermore, when using MeOPEG and GA together the activity increased 370-fold. GA increased the activity of alpha-CT in organic solvent, in spite of its inactivating effect in water. The activating effect of GA was dependent on the water activity (a(w)) at which alpha-CT + GA was equilibrated and on the reaction system. At a(w) 0.06 it was observed at all GA concentrations employed (0.025-0.25%, w/v, in the enzyme water solution before lyophilization), whereas at a(w) 0.96 it was found only at 0.025% GA. Infrared spectroscopic data indicated that prolonged exposure of alpha-CT films to GA in buffer causes changes to the enzyme secondary structure, favoring the hydration of the enzyme, which ultimately suggests a higher accessibility of the substrates to the enzyme. (C) 2012 Elsevier B.V. All rights reserved.
Effects of stabilizing additives on the activity of alpha-chymotrypsin in organic solvent
Secundo Francesco;
2012
Abstract
The ability of ectoin, hydroxyectoin, glycoin (known as extremolytes), glutaraldehyde (GA) and methoxypoly(ethylene glycol) (MeOPEG) to produce formulations of alpha-chymotrypsin (alpha-CT) more active than the native enzyme in organic solvents, was tested. The activity in toluene of lyophilized alpha-CT when ectoin, MeOPEG (1:1, w/w) or GA (0.1%, w/v) were used was 10-, 46-, and 260-fold higher than in the absence of additives, respectively; furthermore, when using MeOPEG and GA together the activity increased 370-fold. GA increased the activity of alpha-CT in organic solvent, in spite of its inactivating effect in water. The activating effect of GA was dependent on the water activity (a(w)) at which alpha-CT + GA was equilibrated and on the reaction system. At a(w) 0.06 it was observed at all GA concentrations employed (0.025-0.25%, w/v, in the enzyme water solution before lyophilization), whereas at a(w) 0.96 it was found only at 0.025% GA. Infrared spectroscopic data indicated that prolonged exposure of alpha-CT films to GA in buffer causes changes to the enzyme secondary structure, favoring the hydration of the enzyme, which ultimately suggests a higher accessibility of the substrates to the enzyme. (C) 2012 Elsevier B.V. All rights reserved.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
