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Interfacial properties of whey protein and whey protein hydrolysates and their influence on O/W emulsion stability

机译:乳清蛋白和乳清蛋白水解物的界面性质及其对O / W乳液稳定性的影响

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摘要

Protein hydrolysates are commonly used in high-tolerance or hypoallergenic formulae. The relation between the physicochemical properties of hydrolysed proteins (i.e., size, molecular weight distribution, charge, hydrophobicity), and their emulsifying properties is not fully understood. In this work, the emulsion forming ability (i. e., the equilibrium between droplet formation and coalescence during emulsification), the gravitational stability, the adsorption kinetics and the interfacial dilatational rheology of whey proteins and whey protein hydrolysates were investigated. More extensive hydrolysis resulted in a progressive decrease of the surface hydrophobicity of the emulsifiers (i. e., whey protein or whey protein hydrolysates). Whey protein was able to form smaller emulsion droplets at low concentrations (< 1 wt%) compared to whey protein hydrolysates (WPH). When the concentration of WPH was in excess (> 2 wt%), similar minimum droplet sizes were obtained due to the adsorption of large peptides. Whey protein-stabilised interfaces showed the lowest interfacial tension and z-potential, which both increased with increasing degree of hydrolysis. Whey protein produced stronger oil-water interfacial layers (i. e., high dilatational moduli and non-linear behavior) and had higher protein surface coverage compared to WPH. Small whey protein peptides (< 5 kDa) formed a weak oil-water interfacial film, which led to unstable emulsions. In whey protein-stabilised emulsions, b-lactoglobulin showed preferential interfacial adsorption over a-lactalbumin. In emulsions containing WPH, large peptides (> 5 kDa) were preferentially adsorbed over small peptides. Emulsion physical stability was strongly influenced by the oil droplet size, and by the formation of an inter-connected viscoelastic film at the oil droplet interface which was observed only for whey protein and peptides with high molecular weight (> 5 kDa). These results should be considered when formulating specialized nutrition emulsions. (C) 2017 Elsevier Ltd. All rights reserved.
机译:蛋白质水解物通常用于高耐受性或低变应原配方中。水解蛋白质的物理化学性质(即大小,分子量分布,电荷,疏水性)与其乳化性质之间的关系尚不完全清楚。在这项工作中,研究了乳清蛋白和乳清蛋白水解物的乳液形成能力(即,乳化过程中液滴形成和聚结之间的平衡),重力稳定性,吸附动力学和界面膨胀流变学。更广泛的水解导致乳化剂(即乳清蛋白或乳清蛋白水解产物)的表面疏水性逐渐降低。与乳清蛋白水解物(WPH)相比,乳清蛋白在低浓度(<1 wt%)时能够形成较小的乳液液滴。当WPH浓度超过(> 2 wt%)时,由于大肽的吸附,获得了相似的最小液滴尺寸。乳清蛋白稳定的界面显示出最低的界面张力和z电位,它们都随着水解程度的增加而增加。与WPH相比,乳清蛋白产生更强的油水界面层(即,高的膨胀模量和非线性行为),并具有更高的蛋白表面覆盖率。乳清蛋白小肽(<5 kDa)形成了弱的油水界面膜,导致乳液不稳定。在乳清蛋白稳定的乳液中,β-乳球蛋白比α-乳白蛋白显示出优先的界面吸附。在含有WPH的乳液中,大肽(> 5 kDa)比小肽优先吸附。乳剂的物理稳定性受油滴大小和油滴界面处相互连接的粘弹性膜形成的强烈影响,只有在高分子量(> 5 kDa)的乳清蛋白和肽中才能观察到。在配制专用营养乳液时应考虑这些结果。 (C)2017 Elsevier Ltd.保留所有权利。

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