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Spreading of Monoglycerides onto beta-Casein Adsorbed Film.Structural and Dilatational Characteristics

机译:甘油单酸酯在β-酪蛋白吸附膜上的扩散结构和膨胀特性

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The effect of monoglycerides (monopalmitin and monoolein) on the structural,topographical,and dilatational characteristics of beta-casein adsorbed film at the air-water interface has been analyzed by means of surface pressure (pi)-area (A) isotherms,Brewster angle microscopy (BAM),and surface dilatational rheology.The static and dynamic characteristics of the mixed films depend on the interfacial composition and the surface pressure.At surface pressures lower than that for the beta-casein collapse (at the equilibrium surface pressure of the protein,pi_e~(beta-casein)) a mixed film of beta-casein and monoglyceride may exist.At higher surface pressures the collapsed beta-casein is partially displaced from the interface by monoglycerides.However,beta-casein displacement by monoglycerides is not quantitative at the monoglyceride concentrations studied in this work.The protein displacement by a monoglyceride is higher for monopalmitin than for monoolein and for spread than for adsorbed films.The viscoelastic characteristics of the mixed films were dominated by the presence of beta-casein in the mixture.Even at the higher surface pressures (at pi > pi_e~(beta-casein)) the small amounts of beta-casein collapsed residues at the interface have a significant effect on the surface dilatational properties of the mixed films.The structural,topographical,and viscoelastic characteristics of the mixed films corroborate the fact that protein displacement for monoglycerides is higher for spread than for adsorbed mixed films.
机译:通过表面压力(pi)-面积(A)等温线,布鲁斯特角分析了甘油一酸酯(monopalmitin和monoolein)对β-酪蛋白吸附膜在空气-水界面的结构,形貌和膨胀特性的影响显微技术(BAM)和表面膨胀流变性。混合膜的静态和动态特性取决于界面组成和表面压力。在表面压力低于β-酪蛋白塌陷的情况下(在蛋白质的平衡表面压力下) β-酪蛋白和甘油单酸酯的混合膜可能存在。在较高的表面压力下,塌陷的β-酪蛋白被甘油单酸酯部分地从界面上置换掉。但是,β-酪蛋白被甘油单酸酯置换的数量不定量单棕榈酸的蛋白质置换率高于单油酸甘油酯和涂抹油的甘油三酸酯的蛋白质置换率高于吸附膜混合膜的粘弹性特征主要由混合物中存在的β-酪蛋白决定,即使在较高的表面压力下(在pi> pi_e〜(β-酪蛋白)处),少量的β-酪蛋白在残基处也会塌陷界面对混合膜的表面膨胀性能有显着影响。混合膜的结构,形貌和粘弹性特性证实了这样的事实,即涂抹甘油单酸酯的蛋白质位移高于吸附混合物的蛋白质位移。

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