Ultrasound-tailored structural remodeling of oleosome-derived proteins enables interfacial engineering and stability of probiotic-loaded high internal phase emulsions.

IF 10.2 1区 化学 Q1 ACOUSTICS
Rongrong Yu, Yuan Huang, Ziyun Tao, Maria Rahman, Shahzad Farooq, Xiu Wang, Juanyan Pan
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引用次数: 0

Abstract

Oleosomes are intracellular lipid-storage organelles found in oilseeds and represent a promising yet underexplored source of proteinaceous emulsifiers for structuring food-grade colloidal systems. In this study, extrinsic proteins (OP) from soybean oleosomes were extracted under controlled alkaline-ultrasonic treatment (0-400 W) to elucidate how ultrasound-mediated protein remodeling governs interfacial adsorption kinetics, high-internal-phase emulsion (HIPE) formation, rheological behavior, and probiotic protection. Alkaline-ultrasonic treatment from 0 to 300 W significantly increased the protein recovery from 40.15% to 58.84%, solubility from 74.10% to 87.61%, and zeta potential from -8.81 to -13.31 mV, while reduced the particle size from 651 to 389 nm. Spectroscopic analyses revealed controlled protein remodeling characterized by increased exposure of hydrophobic and aromatic residues, reduced α-helix content from 22.95% to 15.03%, and increased β-sheet structures from 34.16% to 42.14%. Ultrasonic treatment (300 W) effectively improved the protein diffusion rate (0.106 to 0.182 mNm-1s-0.5) and penetration rate (3.971 × 10-4 to 4.682 × 10-4 s-1) at the oil-water interface, indicating the formation of strengthened interfacial protein films. HIPEs stabilized by OP-300 revealed the smallest droplet size, intensified droplet-droplet interactions, superior viscoelastic properties, and excellent storage stability. LAOS analysis further confirmed that HIPEs prepared with OP-200 and OP-300 maintained structural integrity under large deformation amplitudes ≤100%, compared to the untreated sample ≤10%, indicating the formation of stronger and more cohesive gel networks. Moreover, encapsulated Lactobacillus reuteri showed improved survival rate during simulated digestion, increasing viable cell counts from 4.12 × 107 to 7.21 × 107 CFU/mL. These findings established that ultrasound tailors OP structure-function relationships, enabling their use as sustainable emulsifiers for robust HIPEs with enhanced probiotic delivery.

超声定制的油质体衍生蛋白的结构重塑使益生菌负载高内相乳剂的界面工程和稳定性成为可能。
油小体是在油籽中发现的细胞内脂质储存细胞器,代表了一种有希望但尚未开发的蛋白质乳化剂来源,用于构建食品级胶体系统。在本研究中,在控制碱-超声处理(0-400 W)下提取大豆油小体中的外源蛋白(OP),以阐明超声介导的蛋白质重塑如何影响界面吸附动力学、高内相乳剂(HIPE)形成、流变行为和益生菌保护。在0 ~ 300 W的碱液超声处理下,蛋白质回收率从40.15%提高到58.84%,溶解度从74.10%提高到87.61%,zeta电位从-8.81提高到-13.31 mV,粒径从651减小到389 nm。光谱分析表明,蛋白质的重塑受到控制,其特征是疏水和芳香残基暴露增加,α-螺旋含量从22.95%降低到15.03%,β-片结构从34.16%增加到42.14%。超声处理(300 W)有效提高了蛋白质在油水界面的扩散速率(0.106 ~ 0.182 mNm-1s-0.5)和渗透速率(3.971 × 10-4 ~ 4.682 × 10-4 s-1),界面蛋白膜得到强化。OP-300稳定的HIPEs显示出最小的液滴尺寸,增强的液滴-液滴相互作用,优越的粘弹性性能和优异的储存稳定性。老挝分析进一步证实,与未经处理的样品相比,OP-200和OP-300制备的HIPEs在大变形幅度≤100%时保持了结构完整性,表明形成了更强、更有凝聚力的凝胶网络。此外,在模拟消化过程中,包封的罗伊氏乳杆菌的存活率也有所提高,活菌数从4.12 × 107增加到7.21 × 107 CFU/mL。这些发现表明,超声调整了OP的结构-功能关系,使其能够作为可持续的乳化剂用于增强益生菌输送的强效HIPEs。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ultrasonics Sonochemistry
Ultrasonics Sonochemistry 化学-化学综合
CiteScore
15.80
自引率
11.90%
发文量
361
审稿时长
59 days
期刊介绍: Ultrasonics Sonochemistry stands as a premier international journal dedicated to the publication of high-quality research articles primarily focusing on chemical reactions and reactors induced by ultrasonic waves, known as sonochemistry. Beyond chemical reactions, the journal also welcomes contributions related to cavitation-induced events and processing, including sonoluminescence, and the transformation of materials on chemical, physical, and biological levels. Since its inception in 1994, Ultrasonics Sonochemistry has consistently maintained a top ranking in the "Acoustics" category, reflecting its esteemed reputation in the field. The journal publishes exceptional papers covering various areas of ultrasonics and sonochemistry. Its contributions are highly regarded by both academia and industry stakeholders, demonstrating its relevance and impact in advancing research and innovation.
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