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Effect of homogenization and pasteurization on the structure and stability of whey protein in milk

文献类型： 外文期刊

作者： Qi, Phoebe X. 1 ; Ren, Daxi 2 ; Xiao, Yingping 3 ; Tomasula, Peggy M. 1 ;

作者机构： 1.ARS, Dairy & Funct Foods Res Unit, ERRC, Wyndmoor, PA 19038 USA

2.Zhejiang Univ, Coll Anim Sci, Inst Dairy Sci, Hangzhou 310029, Zhejiang, Peoples R China

3.Zhejiang Acad Agr Sci, Inst Qual & Stand Agroprod, Hangzhou 310021, Zhejiang, Peoples R China

关键词： whey protein;milk processing;molecular structure;spectroscopy;structural stability

期刊名称：JOURNAL OF DAIRY SCIENCE （ 影响因子：4.034； 五年影响因子：4.354 ）

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收录情况： SCI

摘要： The effect of homogenization alone or in combination with high-temperature, short-time (HTST) pasteurization or UHT processing on the whey fraction of milk was investigated using highly sensitive spectroscopic techniques. In pilot plant trials, 1-L quantities of whole milk were homogenized in a 2-stage homogenizer at 35 degrees C (6.9 MPa/10.3 MPa) and, along with skim milk, were subjected to HTST pasteurization (72 degrees C for 15 s) or UHT processing (135 degrees C for 2 s). Other whole milk samples were processed using homogenization followed by either HTST pasteurization or UHT processing. The processed skim and whole milk samples were centrifuged further to remove fat and then acidified to pH 4.6 to isolate the corresponding whey fractions, and centrifuged again. The whey fractions were then purified using dialysis and investigated using the circular dichroism, Fourier transform infrared, and Trp intrinsic fluorescence spectroscopic techniques. Results demonstrated that homogenization combined with UHT processing of milk caused not only changes in protein composition but also significant secondary structural loss, particularly in the amounts of apparent antiparallel beta-sheet and alpha-helix, as well as diminished tertiary structural contact. In both cases of homogenization alone and followed by HTST treatments, neither caused appreciable chemical changes, nor remarkable secondary structural reduction. But disruption was evident in the tertiary structural environment of the whey proteins due to homogenization of whole milk as shown by both the near-UV circular dichroism and Trp intrinsic fluorescence. In-depth structural stability analyses revealed that even though processing of milk imposed little impairment on the secondary structural stability, the tertiary structural stability of whey protein was altered significantly. The following order was derived based on these studies: raw whole > HTST, homogenized, homogenized and pasteurized > skimmed and pasteurized, and skimmed UHT > homogenized UHT. The methodology demonstrated in this study can be used to gain insight into the behavior of milk proteins when processed and provides a new empirical and comparative approach for analyzing and assessing the effect of processing schemes on the nutrition and quality of milk and dairy product without the need for extended separation and purification, which can be both time-consuming and disruptive to protein structures.

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[1]Stabilization of whey protein isolate (WPI) through interactions with sugar beet pectin (SBP) induced by controlled dry-heating. Qi, Phoebe X.,Xiao, Yingping,Wickham, Edward D.,Xiao, Yingping.

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