Department of Food Science, University of Wisconsin-Madison, 1605 Linden Drive, Madison 53706.
Center for Dairy Research, University of Wisconsin-Madison, 1605 Linden Drive, Madison 53706.
J Dairy Sci. 2018 Sep;101(9):7702-7713. doi: 10.3168/jds.2018-14383. Epub 2018 Jun 21.
In recent years, a large increase in the production of milk protein concentrates (MPC) has occurred. However, compared with other types of milk powders, few studies exist on the effect of key processing parameters on powder properties. In particular, it is important to understand if key processing parameters contribute to the poor solubility observed during storage of high-protein MPC powders. Ultrafiltration (UF) and diafiltration (DF) are processing steps needed to reduce the lactose content of concentrates in the preparation of MPC with a protein content of 80% (MPC80). Evaporation is sometimes used to increase the TS content of concentrates before spray drying, and some indications exist that inclusion of this processing step may affect protein properties. In this study, MPC80 powders were manufactured by 2 types of concentration methods: membrane filtration with and without the inclusion of an evaporation step. Different concentration methods could affect the mineral content of MPC powders, as soluble salts can permeate the UF membrane, whereas no mineral loss occurs during evaporation, although a shift in calcium equilibrium toward insoluble forms may occur at high protein concentration levels. It is more desirable from an energy efficiency perspective to use higher total solids in concentrates before drying, but concerns exist about whether a higher protein content would negatively affect powder functionality. Thus, MPC80 powders were also manufactured from concentrates that had 3 different final protein concentrations (19, 21, and 23%; made from 1 UF retentate using batch recirculation evaporation, a similar concentration method). After manufacture, powders were stored for 6 mo at 30°C to help understand changes in MPC80 properties that might occur during shelf-life. Solubility and foaming properties were determined at various time points during high-temperature powder storage. Inclusion of an evaporation step, as a concentration method, resulted in MPC80 that had higher ash, total calcium, and bound calcium (of rehydrated powder) contents compared to concentration with only membrane filtration. Concentration method did not significantly affect the bulk (tapped) density, solubility, or foaming properties of the MPC powders. Powder produced from concentrate with 23% protein content exhibited a higher bulk density and powder particle size than powder produced from concentrate that had 19% protein. The solubility of MPC80 powder was not influenced by the protein content of the concentrate. The solubility of all powders significantly decreased during storage at 30°C. Higher protein concentrations in concentrates resulted in rehydrated powders that had higher viscosities (even when tested at a constant protein concentration). The protein content of the concentrate did not significantly affect foaming properties. Significant changes in the mineral content are used commercially to improve MPC80 solubility. However, although the concentration method did produce a small change in the total calcium content of experimental MPC80 samples, this modification was not sufficiently large enough (<7%) to influence powder solubility.
近年来,牛奶蛋白浓缩物(MPC)的产量大幅增加。然而,与其他类型的奶粉相比,关于关键加工参数对粉末性质影响的研究很少。特别是,了解关键加工参数是否会导致高蛋白 MPC 粉末在储存过程中出现较差的溶解度非常重要。超滤(UF)和渗滤(DF)是在制备蛋白质含量为 80%的 MPC(MPC80)时降低浓缩物中乳糖含量所需的加工步骤。蒸发有时用于在喷雾干燥前增加浓缩物的总固形物含量,并且有一些迹象表明,包括此加工步骤可能会影响蛋白质性质。在这项研究中,通过两种浓缩方法制造了 MPC80 粉末:包含和不包含蒸发步骤的膜过滤。不同的浓缩方法可能会影响 MPC 粉末的矿物质含量,因为可溶性盐可以渗透 UF 膜,而在蒸发过程中不会损失矿物质,尽管在高蛋白质浓度水平下,钙平衡可能会向不溶性形式转移。从能量效率的角度来看,在干燥之前使用更高的总固体含量更可取,但人们担心更高的蛋白质含量是否会对粉末功能产生负面影响。因此,还使用 3 种不同最终蛋白质浓度(19%、21%和 23%)的浓缩物制造了 MPC80 粉末(使用批循环蒸发从 1 个 UF 保留物制成,这是一种类似的浓缩方法)。在制造后,将粉末在 30°C 下储存 6 个月,以帮助了解在保质期内可能发生的 MPC80 性质变化。在高温粉末储存过程中的各个时间点测定溶解度和泡沫性能。作为浓缩方法,包含蒸发步骤会导致 MPC80 的灰分、总钙和结合钙(复水粉末)含量高于仅通过膜过滤的浓缩物。浓缩方法对 MPC 粉末的堆积(轻敲)密度、溶解度或泡沫性能没有显著影响。由蛋白质含量为 23%的浓缩物生产的粉末的堆积密度和粉末粒径均高于由蛋白质含量为 19%的浓缩物生产的粉末。浓缩物的蛋白质含量不影响 MPC80 粉末的溶解度。在 30°C 下储存时,所有粉末的溶解度均显著降低。浓缩物中的较高蛋白质浓度导致复水粉末的粘度增加(即使在恒定蛋白质浓度下测试也是如此)。浓缩物的蛋白质含量对泡沫性能没有显著影响。商业上使用矿物质含量的变化来改善 MPC80 的溶解度。然而,尽管浓缩方法确实使实验性 MPC80 样品的总钙含量略有变化,但这种变化不够大(<7%),不会影响粉末的溶解度。