Siew D C, Heilmann C, Easteal A J, Cooney R P
Industrial Research Limited, Auckland, New Zealand.
J Agric Food Chem. 1999 Aug;47(8):3432-40. doi: 10.1021/jf9806311.
The aim of this study is to determine the effects of plasticizer hydrogen bonding capability and chain length on the molecular structure of sodium caseinate (NaCAS), in NaCAS/glycerol and NaCAS/polyethylene glycol 400 (PEG) systems. Both solution and film phases were investigated. Glycerol and PEG reduced the viscosity of aqueous NaCAS, with the latter having a greater effect. This was explained in terms of protein/plasticizer aggregate size and changes to the conformation of the caseinate chain. In the film phase, glycerol caused more pronounced changes to the film tensile strength compared with PEG. However, the effect of glycerol on film water vapor permeability was smaller. These observations are attributed to the differences in plasticizer size and hydrogen bonding strength that controls the protein-plasticizer and protein-protein interactions in the films. Glass transition calculations from the tensile strength data indicate that the distribution of bonding interactions is more homogeneous in NaCAS/PEG films than in NaCAS/glycerol films.
本研究的目的是确定在酪蛋白酸钠(NaCAS)/甘油和NaCAS/聚乙二醇400(PEG)体系中,增塑剂的氢键能力和链长对NaCAS分子结构的影响。对溶液相和薄膜相都进行了研究。甘油和PEG降低了NaCAS水溶液的粘度,其中PEG的影响更大。这可以从蛋白质/增塑剂聚集体尺寸以及酪蛋白链构象的变化方面来解释。在薄膜相中,与PEG相比,甘油对薄膜拉伸强度的影响更为显著。然而,甘油对薄膜水蒸气透过率的影响较小。这些观察结果归因于增塑剂尺寸和氢键强度的差异,它们控制着薄膜中蛋白质-增塑剂和蛋白质-蛋白质的相互作用。根据拉伸强度数据进行的玻璃化转变计算表明,与NaCAS/甘油薄膜相比,NaCAS/PEG薄膜中键合相互作用的分布更为均匀。