Patel Hasmukh A, Singh Harjinder, Anema Skelte G, Creamer Lawrence K
Fonterra Research Centre, Private Bag 11 029, Palmerston North, New Zealand.
J Agric Food Chem. 2006 May 3;54(9):3409-20. doi: 10.1021/jf052834c.
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 degrees C). The pasteurizing heat treatment (72 degrees C for 15 s) denatured and aggregated only a few minor whey proteins, but the high heat treatments (100 degrees C for 120 s, 120 degrees C for 120 s, and 140 degrees 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)-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.
传统上,牛奶经过热处理以控制微生物并改变其功能,例如提高其热稳定性。压力处理已被视为控制微生物的一种可能替代方法,但一些与功能相关的乳蛋白相互作用尚未得到探索。本研究使用两种新型二维聚丙烯酰胺凝胶电泳(2D PAGE)方法,来探究四种常见热处理以及在环境温度(22摄氏度)下200、400、600和800兆帕压力处理30分钟后,乳蛋白中不可逆二硫键变化的差异。巴氏杀菌热处理(72摄氏度15秒)仅使少数几种次要乳清蛋白变性和聚集,但高温处理(100摄氏度120秒、120摄氏度120秒和140摄氏度5秒)形成了二硫键连接的聚集体,其中包含所有乳清蛋白和κ-酪蛋白(κ-CN)的很大比例以及一部分αs2-CN。在200兆帕压力下对牛奶进行处理会使β-乳球蛋白(β-LG)形成二硫键连接的二聚体,并将β-LG纳入聚集体,可能是与κ-CN形成二硫键连接。其他乳清蛋白在200兆帕处理30分钟时似乎受影响较小。相比之下,800兆帕压力处理会将β-LG和大多数次要乳清蛋白以及κ-CN和大部分αs2-CN纳入聚集体。压力处理牛奶中αs2-CN的可及性以及涉及αs2-CN、κ-CN和乳清蛋白的复合物的形成是一个重要的新发现。然而,只有一部分α-乳白蛋白变性或纳入大聚集体中。这些以及其他结果表明,蛋白质稳定性以及高温或高压下蛋白质二硫键可及性之间的差异,会影响形成途径,从而导致所得聚集体之间存在差异、聚集体大小不同以及产品功能各异。