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朝着预测蛋白稳定乳液的稳定性的方向发展。

Towards predicting the stability of protein-stabilized emulsions.

机构信息

Laboratory of Food Chemistry, Wageningen University, Bornse Weilanden 9, 6708 WG Wageningen, The Netherlands.

AVEBE, Prins Hendrikplein 20, 9641 GK Veendam, The Netherlands.

出版信息

Adv Colloid Interface Sci. 2015 May;219:1-9. doi: 10.1016/j.cis.2015.01.008. Epub 2015 Feb 7.

Abstract

The protein concentration is known to determine the stability against coalescence during formation of emulsions. Recently, it was observed that the protein concentration also influences the stability of formed emulsions against flocculation as a result of changes in the ionic strength. In both cases, the stability was postulated to be the result of a complete (i.e. saturated) coverage of the interface. By combining the current views on emulsion stability against coalescence and flocculation with new experimental data, an empiric model is established to predict emulsion stability based on protein molecular properties such as exposed hydrophobicity and charge. It was shown that besides protein concentration, the adsorbed layer (i.e. maximum adsorbed amount and interfacial area) dominates emulsion stability against coalescence and flocculation. Surprisingly, the emulsion stability was also affected by the adsorption rate. From these observations, it was concluded that a completely covered interface indeed ensures the stability of an emulsion against coalescence and flocculation. The contribution of adsorption rate and adsorbed amount on the stability of emulsions was combined in a surface coverage model. For this model, the adsorbed amount was predicted from the protein radius, surface charge and ionic strength. Moreover, the adsorption rate, which depends on the protein charge and exposed hydrophobicity, was approximated by the relative exposed hydrophobicity (QH). The model in the current state already showed good correspondence with the experimental data, and was furthermore shown to be applicable to describe data obtained from literature.

摘要

蛋白质浓度已知会影响乳状液形成过程中抵抗聚结的稳定性。最近观察到,由于离子强度的变化,蛋白质浓度也会影响形成的乳状液抵抗絮凝的稳定性。在这两种情况下,稳定性被假定为界面完全(即饱和)覆盖的结果。通过将目前关于乳状液抗聚结和絮凝稳定性的观点与新的实验数据结合起来,建立了一种经验模型,该模型基于蛋白质的分子特性,如暴露的疏水性和电荷,来预测乳状液的稳定性。结果表明,除了蛋白质浓度外,吸附层(即最大吸附量和界面面积)也会影响乳状液的抗聚结和絮凝稳定性。令人惊讶的是,乳状液的稳定性也受到吸附速率的影响。从这些观察结果可以得出结论,完全覆盖的界面确实可以确保乳状液的抗聚结和絮凝稳定性。吸附速率和吸附量对乳状液稳定性的影响被结合在一个表面覆盖模型中。对于该模型,吸附量是根据蛋白质半径、表面电荷和离子强度来预测的。此外,吸附速率取决于蛋白质的电荷和暴露的疏水性,可通过相对暴露的疏水性(QH)来近似。该模型目前已经与实验数据有很好的一致性,并且还可以应用于描述从文献中获得的数据。

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