摘要 : Traditionally,milk has been heat treated to control microorganisms and to alter its functionality,for example,to increase its heat stability.Pressure treatment has been considered as a possible alternative for microorganism contro... 展开 Traditionally,milk has been heat treated to control microorganisms and to alter its functionality,for example,to increase its heat stability.Pressure treatment has been considered as a possible alternative for microorganism control,but some of the functionality-related milk protein interactions have not been explored.The present study used two novel two-dimensional polyacrylamide gel electrophoresis (2D PAGE)methods to explore the differences in the irreversible disulfide bond changes among the milk proteins after four common heat treatments and after 30-min pressure treatments of milk at 200,400,600,and 800 MPa at ambient temperature (22 deg C).The pasteurizing heat treatment (72 deg C for 15 s)denatured and aggregated only a few minor whey proteins,but the high heat treatments (100 deg C for 120 s,120 deg C for 120 s,and 140 deg C for 5 s)formed disulfide-bonded aggregates that included a high proportion of all of the whey proteins and kappa-casein (kappa-CN)and a proportion of the alpha_(s2)-CN.Pressure treatment of milk at 200 MPa caused beta-lactoglobulin (beta-LG)to form disulfide-bonded dimers and incorporated beta-LG into aggregates,probably disulfide-bonded to kappa-CN.The other whey proteins appeared to be less affected at 200 MPa for 30 min.In contrast,pressure treatment at 800 MPa incorporated beta-LG and most of the minor whey proteins,as well as kappa-CN and much of the alpha_(s2)-CN,into aggregates.The accessibility of alpha_(s2)-CN and formation of complexes involving alpha_(s2)s2-CN,kappa-CN,and whey proteins in the pressure treated milk is an important novel finding.However,only some of the alpha-lactalbumin was denatured or incorporated into the large aggregates.These and other results show that the differences between the stabilities of the proteins and the accessibilities of the disulfide bonds of the proteins at high temperature or pressure affect the formation pathways that give the differences among the resultant aggregates,the sizes of the aggregates,and the product functionalities. 收起