Pectinesterase, lipase, polyphenol oxidase, lipoxygenase, peroxidase,
lactoperoxidase, phosphatase and catalase have been examined at distin
ct conditions within a pressure range of 0.1 to 900 MPa, temperatures
from 25 degrees C to 60 degrees C, pH 3 to 7, and time of treatment of
2 min to 45 min. Results in model buffers made it possible to rank th
r enzymes according to their pressure induced inactivation in the foll
owing order: lipoxygenase, lactoperoxidase, pectinesterase, lipase, ph
osphatase, catalase, polyphenol oxidase, peroxidase. A combination of
pressure with moderate temperature increased the degree of enzyme inac
tivation. Pressure treatment of real food systems showed a protective
effect of food ingredients on the pressure inactivation of most enzyme
s evaluated. For example sucrose protected pectinesterase from inactiv
ation by pressure while lactoperoxidase and lipoxigenase were as stabl
e in milk as in buffer.