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通过电泳和圆二色光谱研究发现,β-乳球蛋白是加工牛奶中的一种热标志物。

Beta-lactoglobulin is a thermal marker in processed milk as studied by electrophoresis and circular dichroic spectra.

作者信息

Chen W L, Hwang M T, Liau C Y, Ho J C, Hong K C, Mao S J T

机构信息

Research Institute of Biochemical Engineering, Department of Biological Science and Technology, National Chiao Tung University, Hsinchu, Taiwan, Republic of China.

出版信息

J Dairy Sci. 2005 May;88(5):1618-30. doi: 10.3168/jds.S0022-0302(05)72833-2.

Abstract

As much of the sterilization process involves heat treatment during the preparation of milk on an industrial scale, the unpredictable measures of the process are an essential issue in determining the quality of the milk. The purpose of the present study was to investigate the major protein change(s) of whey proteins in processed milk and extend the knowledge for future reference in the dairy industry. Using a native polyacrylamide gel electrophoresis, we showed almost a 90% loss and denaturation of beta-lactoglobulin (LG), but not alpha-lactalbumin (LA), in some brands of the processed and dry milks. Immunochemical analysis using Western blotting revealed that part of the loss was attributed to the formation of large multiple forms of LG in the processed product. Such denaturation was presumably associated with the heating procedure used in the process. Essentially, LG was the only major fraction converted to aggregates in milk heated at 95 degrees C for 30 min on 2-dimensional PAGE. The detailed thermal denaturation of purified LG and LA at various temperatures (50 to 95 degrees C) and time (5 to 960 s) were investigated using a circular dichroic analysis. The maximal changes of ellipticity at 205 nm (converting beta-structure to disordered structure) were correlated to heating temperature and time. There were no significant conformational changes of LG at temperatures below 70 degrees C for as long as 480 s. Pronounced and rapid changes occurred between 80 to 95 degrees C in a time-dependent manner. Fifty percent of the maximal changes could be reached within 15 s. In conclusion, the unique chemical and immunochemical loss and conformational changes made LG a superior marker for evaluating the thermal processing of milk. The detailed thermal denaturation curves of LG constructed with its time and temperature in this study provide a valuable reference for the dairy industry. We postulate that heat treatment over 80 degrees C in 15 s may induce a significant denaturation of milk LG.

摘要

由于在工业规模制备牛奶的过程中,大部分杀菌过程涉及热处理,因此该过程中不可预测的因素是决定牛奶质量的关键问题。本研究的目的是调查加工牛奶中乳清蛋白的主要蛋白质变化,并扩展相关知识以供乳制品行业未来参考。通过使用天然聚丙烯酰胺凝胶电泳,我们发现某些品牌的加工牛奶和奶粉中,β-乳球蛋白(LG)几乎损失并变性了90%,而α-乳白蛋白(LA)则没有。使用蛋白质免疫印迹法进行的免疫化学分析表明,部分损失归因于加工产品中形成了多种形式的大分子LG。这种变性可能与加工过程中使用的加热程序有关。从本质上讲,在二维聚丙烯酰胺凝胶电泳上,LG是在95摄氏度加热30分钟的牛奶中唯一转化为聚集体的主要成分。使用圆二色性分析研究了纯化的LG和LA在不同温度(50至95摄氏度)和时间(5至960秒)下的详细热变性情况。在205纳米处椭圆率的最大变化(从β-结构转变为无序结构)与加热温度和时间相关。在低于70摄氏度的温度下长达480秒,LG没有明显的构象变化。在80至95摄氏度之间,以时间依赖的方式发生了明显且快速的变化。在15秒内可达到最大变化的50%。总之,独特的化学和免疫化学损失以及构象变化使LG成为评估牛奶热处理的优良标志物。本研究中构建的LG随时间和温度变化的详细热变性曲线为乳制品行业提供了有价值的参考。我们推测,在15秒内超过80摄氏度的热处理可能会导致牛奶LG发生显著变性。

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