Liang Ningjian, Koh Jeewon, Kim Bum Jin, Ozturk Gulustan, Barile Daniela, Dallas David C
Nutrition Program, School of Biological and Population Health Sciences, College of Public Health and Human Sciences, Oregon State University, Corvallis, OR, United States.
Department of Food Science and Technology, University of California, Davis, Davis, CA, United States.
Front Nutr. 2022 Sep 15;9:926814. doi: 10.3389/fnut.2022.926814. eCollection 2022.
Donor human milk should be processed to guarantee microbiological safety prior to infant feeding, but this process can influence the structure and quantity of functional proteins.
The aim of this study was to determine the effect of thawing, homogenization, vat-pasteurization (Vat-PT), retort sterilization (RTR) and ultra-high-temperature (UHT) processing on the structure of bioactive proteins in donor milk.
Pooled donor milk was either not treated (Raw) or treated with an additional freeze-thaw cycle with and without homogenization, Vat-PT, RTR with and without homogenization, and UHT processing with and without homogenization. Overall protein retention was assessed sodium-dodecyl sulfate (SDS-PAGE), and the immunoreactivity of 13 bioactive proteins were assessed enzyme-linked immunosorbent assay (ELISA).
Freeze-thawing, freeze-thawing plus homogenization and Vat-PT preserved all the immunoglobulins (sIgA/IgA, IgG, IgM) in donor milk, whereas RTR and UHT degraded almost all immunoglobulins. UHT did not alter osteopontin immunoreactivity, but Vat-PT and retort decreased it by ~50 and 70%, respectively. Freeze-thawing with homogenization, Vat-PT and UHT reduced lactoferrin's immunoreactivity by 35, 65, and 84%, respectively. Lysozyme survived unaltered throughout all processing conditions. In contrast, elastase immunoreactivity was decreased by all methods except freeze-thawing. Freeze-thawing, freeze-thawing plus homogenization and Vat-PT did not alter polymeric immunoglobulin receptor (PIGR) immunoreactivity, but RTR, RTR plus homogenization and UHT increased detection. All heat processing methods increased α-lactalbumin immunoreactivity. Vat-PT preserved all the growth factors (vascular/endothelial growth factor, and transforming growth factors β1 and β2), and UHT treatments preserved the majority of these factors.
Different bioactive proteins have different sensitivity to the treatments tested. Overall, Vat-PT preserved more of the bioactive proteins compared with UHT or RTR. Therefore, human milk processors should consider the impact of processing methods on key bioactive proteins in human milk.
捐赠的人乳在用于婴儿喂养之前应进行处理以确保微生物安全,但此过程可能会影响功能蛋白的结构和数量。
本研究旨在确定解冻、均质化、巴氏杀菌、高温高压灭菌和超高温处理对捐赠人乳中生物活性蛋白结构的影响。
将汇集的捐赠人乳分为未处理组(生鲜组),以及经过额外冻融循环且有无均质化处理的组、巴氏杀菌组、有无均质化处理的高温高压灭菌组和有无均质化处理的超高温处理组。通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)评估总蛋白保留情况,并通过酶联免疫吸附测定(ELISA)评估13种生物活性蛋白的免疫反应性。
冻融、冻融加均质化以及巴氏杀菌可保留捐赠人乳中的所有免疫球蛋白(分泌型IgA/IgA、IgG、IgM),而高温高压灭菌和超高温处理几乎会降解所有免疫球蛋白。超高温处理未改变骨桥蛋白的免疫反应性,但巴氏杀菌和高温高压灭菌分别使其降低了约50%和70%。冻融加均质化、巴氏杀菌和超高温处理分别使乳铁蛋白的免疫反应性降低了35%、65%和84%。溶菌酶在所有处理条件下均未发生变化。相比之下,除冻融外,所有处理方法均降低了弹性蛋白酶的免疫反应性。冻融、冻融加均质化以及巴氏杀菌未改变聚合免疫球蛋白受体(PIGR)的免疫反应性,但高温高压灭菌、高温高压灭菌加均质化以及超高温处理增加了其检测值。所有热处理方法均增加了α-乳白蛋白的免疫反应性。巴氏杀菌保留了所有生长因子(血管/内皮生长因子以及转化生长因子β1和β2),超高温处理保留了这些因子中的大部分。
不同的生物活性蛋白对所测试的处理方法具有不同的敏感性。总体而言,与超高温处理或高温高压灭菌相比,巴氏杀菌保留了更多的生物活性蛋白。因此,人乳加工者应考虑加工方法对人乳中关键生物活性蛋白的影响。