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马铃薯蛋白基微凝胶的体相和界面行为。

Bulk and Interfacial Behavior of Potato Protein-Based Microgels.

机构信息

Food Colloids and Bioprocessing Group, School of Food Science and Nutrition, University of Leeds, Leeds LS2 9JT, U.K.

Molecular and Nanoscale Physics Group, School of Physics and Astronomy, University of Leeds, Leeds LS2 9JT, U.K.

出版信息

Langmuir. 2024 Oct 15;40(41):21341-21351. doi: 10.1021/acs.langmuir.4c01785. Epub 2024 Oct 1.

Abstract

This study aims to understand the bulk and interfacial performance of potato protein microgels. Potato protein (PoP) was used to produce microgels of submicrometer diameter via a top-down approach of thermal cross-linking followed by high-shear homogenization of the bulk gel. Bulk "parent" gels were formed at protein concentrations [PoP] = 5-18 wt %, which subsequently varied in their bulk shear elastic modulus (') by several orders of magnitude (1-100 kPa), ' increasing with increasing [PoP]. The PoP microgels (PoPM) formed from these parent gels had diameters varying between 100 and 300 nm (size increasing with increasing ' and [PoP]), as observed via dynamic light scattering and atomic force microscopy (AFM) of PoPM adsorbed onto silicon. Interfacial rheology (interfacial shear storage and loss moduli, ' and ″) and interfacial tension (γ) of adsorbed films of PoP (i.e., nonheated PoP) and PoPM (both at tetradecane-water interfaces) were also studied, as well as the bulk rheology of the PoPM dispersions. The results showed that PoPM dispersions (at 50 vol %) had significantly higher bulk viscosity and shear thinning properties compared to the nonmicrogelled PoP at the same overall [PoP], but the bulk rheological behavior was in sharp contrast to the interfacial rheological performance, where ' and ″ of PoP were higher than for any of the PoPM. This suggests that the deformability and size of the microgels were key in determining the interfacial rheology of the PoPM. These findings may be attributed to the limited capacity for "unfolding" and lateral interactions of the larger PoPM at the interface, which are presumed to be stiffer due to their production from the strongest PoP gels. Our study further confirmed that heating and cooling the adsorbed films of PoPM after their adsorption showed little change, highlighting that hydrogen bonding was limited between the microgel particles.

摘要

本研究旨在了解马铃薯蛋白微球的体相和界面性能。采用自上而下的方法,通过热交联和随后的大块凝胶高剪切均化,将马铃薯蛋白(PoP)制成亚微米直径的微球。大块“母体”凝胶在蛋白质浓度[PoP] = 5-18wt%下形成,随后其体相剪切弹性模量(')变化了几个数量级(1-100kPa),'随[PoP]的增加而增加。从这些母体凝胶中形成的马铃薯蛋白微球(PoPM)的直径在 100-300nm 之间变化(随着'和[PoP]的增加而增大),这是通过吸附在硅上的 PoPM 的动态光散射和原子力显微镜(AFM)观察到的。还研究了 PoP(即未经加热的 PoP)和 PoPM(均在十四烷-水界面上)吸附膜的界面流变学(界面剪切储能模量和损耗模量'和")和界面张力(γ),以及 PoPM 分散体的体相流变学。结果表明,与相同总[PoP]下的非微凝胶化的 PoP 相比,PoPM 分散体(在 50vol%下)具有显著更高的体相粘度和剪切稀化特性,但体相流变行为与界面流变性能形成鲜明对比,其中 PoP 的'和"高于任何 PoPM。这表明微球的变形性和尺寸是决定 PoPM 界面流变学的关键。这些发现可能归因于在界面上较大的 PoPM 的“展开”和横向相互作用的能力有限,由于它们是由最强的 PoP 凝胶生产的,因此被认为更硬。我们的研究进一步证实,在吸附后加热和冷却 PoPM 的吸附膜几乎没有变化,这突出表明氢键在微凝胶颗粒之间是有限的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be87/11483775/1b28656830c0/la4c01785_0001.jpg

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