商品β-葡聚糖与萃取β-葡聚糖的理化比较及酶纯化后的结构表征

S. M. V. Mejía, A. D. Francisco, P. Barreto, B. Mattioni, A. W. Zibetti, L. Molognoni, H. Daguer
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引用次数: 3

摘要

背景:β-葡聚糖(1- 3,1 -4)是一种可溶纤维,由于其技术特性(水结合能力、粘度、乳化和稳定)及其对健康的有益影响而应用于食品中。β-葡聚糖的功能特性在提取和纯化过程中会丧失。β-葡聚糖的高粘度与其在肠道中的高分子量及其生理特性有关。因此,在提取和纯化后对纤维进行表征是了解其在食品中的可能应用的基础。目的:表征β-葡聚糖提取物(e - β g),并将其与三种商品β-葡聚糖(c - β g - a、c - β g - b和c - β g - c)进行比较,以确定其在食品中的可能应用,并评估酶纯化是否会影响β-葡聚糖的分子和结构。方法:提取大麦β-葡聚糖(e - β g),对其进行化学分析、流变学行为和颜色表征,并与3种市售样品进行比较。然后对提取液进行纯化,计算其结构和分子特性。结果:EβG β-葡聚糖含量为64.38±3.54%,淀粉污染高(12.70±1.73%),钙含量高(8894 mg/kg),具有假塑性行为,颜色深(L* = 52.77±0.7)。所有商业样品显示低淀粉污染,较浅的颜色,和牛顿行为。纯化后淀粉和蛋白质污染降低(分别为0.85±0.46%和5.50±0.12%),βG含量提高(69.45±0.81%),亮度提高(L* = 92.60±1.70)。纯化后的β-葡聚糖(p - β g)分子量为690±1.6 kDa,在结构上鉴定出聚合度为3 (DP3) ~ 11 (DP11)的物质。结论:纯化前的EβG提取物粘度高,污染严重。酶净化过程是有效的,并允许保持高摩尔质量的p - β g及其独特的分子结构(具有DP3和DP4的物种)。商品样品CβG-A和CβG-B β-葡聚糖含量低。结果表明,c - β g - c具有较好的理化和流变性能,可用于食品加工。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PHYSICOCHEMICAL COMPARISON OF COMMERCIAL VS. EXTRACTED β-GLUCANS AND STRUCTURAL CHARACTERIZATION AFTER ENZYMATIC PURIFICATION
Background: β-glucans (1-3: 1-4) are soluble fibers applied to foods due to their technological properties (water binding capacity, viscosity, emulsification and stabilization) and their beneficial effects on health. The functional properties of β-glucans can be lost during the extraction and purification processes. The high viscosity of β-glucans is related to a high molecular weight and its physiological properties in the intestine. Therefore, to characterize the fiber after its extraction and purification is fundamental to understand its possible applications in foods. Objectives: characterize β-glucans extracted (EβG) and compare them with three commercial β-glucans (CβG-A, CβG-B and CβG-C) to identify its possible applications in foods and to evaluate if enzymatic purification affects molecular and structurally the β-glucans. Methods: barley β-glucans were extracted (EβG), characterized by chemical analyzes, rheological behavior, and color, and compared to three commercial β-glucans samples. Then, the extract was purified and its structural and molecular characteristics were calculated. Results: EβG contained 64.38 ± 3.54% of β-glucans, high starch contamination (12.70 ± 1.73%), high content of calcium (8894 mg/kg), pseudoplastic behavior, and dark color (L* = 52.77 ± 0.7). All commercial samples showed low starch contamination, lighter color, and Newtonian behavior. After purification starch and protein contamination decreased (0.85 ± 0.46% and 5.50 ± 0.12% respectively), increased the content of βG (69.45 ± 0.81%) and increased brightness (L* = 92.60 ± 1.70). Purified β-glucans (PβG) showed a molar weight of 690 ± 1.6 kDa and species with degree polymerization 3 (DP3) to 11 (DP11) were identified on the structure. Conclusions: EβG extracts before the purification presented a high viscosity and contamination. The enzymatic purification process was effective and allowed to maintain a high molar mass of PβG and its distinctive molecular structures (species with DP3 and DP4). The commercial samples CβG-A and CβG-B showed a low content of β-glucans. Finally, CβG-C presented the best physicochemical and rheological properties for its subsequent application in food.
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