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可溶性淀粉对微生物转谷氨酰胺酶诱导的牛血清白蛋白冷置凝胶的影响及机制:一种显著改良的活性物质载体

Effect and Mechanism of Soluble Starch on Bovine Serum Albumin Cold-Set Gel Induced by Microbial Transglutaminase: A Significantly Improved Carrier for Active Substances.

作者信息

Shi Haoting, Ding Changsheng, Yuan Jianglan

机构信息

Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), College of Bioengineering and Food, Hubei University of Technology, Wuhan 430068, China.

出版信息

Foods. 2023 Nov 29;12(23):4313. doi: 10.3390/foods12234313.

Abstract

Soluble starch (SS) could significantly accelerate the process of bovine serum albumin (BSA) cold-set gelation by glucono-δ-lactone (GDL) and microbial transglutaminase (MTGase) coupling inducers, and enhance the mechanical properties. Hardness, WHC, loss modulus (G″) and storage modulus (G') of the gel increased significantly, along with the addition of SS, and gelation time was also shortened from 41 min (SS free) to 9 min (containing 4.0% SS); the microstructure also became more and more dense. The results from FTIR, fluorescence quenching and circular dichroism (CD) suggested that SS could bind to BSA to form their composites, and the hydrogen bond was probably the dominant force. Moreover, the ability of SS to bind the original free water in BSA gel was relatively strong, thereby indirectly increasing the concentration of BSA and improving the texture properties of the gel. The acceleration of gelling could also be attributed to the fact that SS reduced the negative charge of BSA aggregates and further promoted the rapid formation of the gel. The embedding efficiency (EE) of quercetin in BSA-SS cold-set gel increased from 68.3% (SS free) to 87.45% (containing 4.0% SS), and a controlled-released effect was detected by simulated gastrointestinal digestion tests. The work could put forward new insights into protein gelation accelerated by polysaccharide, and provide a candidate for the structural design of new products in the food and pharmaceutical fields.

摘要

可溶性淀粉(SS)可通过葡萄糖酸 - δ - 内酯(GDL)和微生物转谷氨酰胺酶(MTGase)偶联诱导剂显著加速牛血清白蛋白(BSA)的冷胶凝过程,并增强其机械性能。随着SS的添加,凝胶的硬度、持水能力、损耗模量(G″)和储能模量(G')显著增加,胶凝时间也从41分钟(无SS)缩短至9分钟(含4.0% SS);微观结构也变得越来越致密。傅里叶变换红外光谱(FTIR)、荧光猝灭和圆二色性(CD)结果表明,SS可与BSA结合形成复合物,氢键可能是主要作用力。此外,SS结合BSA凝胶中原始自由水的能力较强,从而间接提高了BSA的浓度并改善了凝胶的质地特性。胶凝加速还可归因于SS降低了BSA聚集体的负电荷,进一步促进了凝胶的快速形成。槲皮素在BSA - SS冷胶凝中的包封效率(EE)从68.3%(无SS)提高到87.45%(含4.0% SS),通过模拟胃肠消化试验检测到了控释效果。该研究可为多糖加速蛋白质凝胶化提供新的见解,并为食品和制药领域新产品的结构设计提供候选方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daf1/10706570/9a107dbec924/foods-12-04313-g001.jpg

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