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A micro- and macro-scale approach to probe the dynamics of sol-gel transition in cereal β-glucan solutions varying in molecular characteristics

机译:微观和宏观方法探讨分子特性变化的谷物β-葡聚糖溶液中溶胶-凝胶转变的动力学

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Cereal β-glucans are known to display functional properties with health benefits, such as reduction of plasma cholesterol and of postprandial serum glucose levels in humans and animals; such effects have been lately attributed to viscosity and gelation potential of these water soluble fibres. The local dynamics of β-glucan solutions differing in molecular size and the molar ratio of trimers to tetramers (DP3/DP4) chain segments, which undergo gelation upon ageing, was investigated. Confocal microscopy, particle tracking microrheology and conventional bulk shear Theological measurements have been employed to study the microstructure and mechanical properties of the polysaccharide networks on various length scales. The structural features of β-glucans, such as molecular weight and ratio of DP3/DP4, were found to be important determinants of their gelling properties and microstructure. For the β-glucan gels cured at 25 ℃ both the microrheology and the bulk rheology revealed that with decreasing molecular weight and increasing DP3/DP4 molar ratio the gelation time decreased, while the gelation rate increased along with the storage modulus. In all samples studied, particulate clusters of β-glucan assemblies were generated with size ~ 1-15 μm and the clusters were eventually interconnected to expand over the available space to form an elastic network. The pore size and the structural entities were found to increase in size at lower values of the DP3/DP4 molar ratio and with preparations of high molecular weight. The size and the compactness of the structural entities seem to play an important role in the network reinforcement. The embedded tracer particles were found to experience relatively homogeneous microenvironments at DP3/DP4 ~2.1, reflecting a rather slow rate of chain aggregates structuring. The behaviour of the polysaccharide network dynamics at a microscopic level does not always seem to match the overall bulk macroscopic response.
机译:已知谷类β-葡聚糖具有有益健康的功能特性,例如降低人和动物的血浆胆固醇和餐后血清葡萄糖水平。这些作用最近归因于这些水溶性纤维的粘度和胶凝潜力。研究了在老化后发生凝胶化的分子大小和三聚体与四聚体(DP3 / DP4)链段的摩尔比不同的β-葡聚糖溶液的局部动力学。共聚焦显微镜,颗粒跟踪微观流变学和常规的整体剪切流变学测量已被用于研究各种长度尺度上多糖网络的微观结构和力学性能。发现β-葡聚糖的结构特征,例如分子量和DP3 / DP4的比率,是决定其胶凝性能和微观结构的重要因素。对于在25℃固化的β-葡聚糖凝胶,其微观流变学和本体流变学均表明,随着分子量的降低和DP3 / DP4摩尔比的增加,胶凝时间缩短,而胶凝速率随储能模量的增加而增加。在所有研究的样品中,都生成了大小约为1-15μm的β-葡聚糖组件颗粒簇,这些簇最终相互连接以在可用空间上扩展以形成弹性网络。发现在较低的DP3 / DP4摩尔比值和高分子量制剂下,孔径和结构实体的尺寸增加。结构实体的大小和紧凑性似乎在网络加强中起着重要作用。发现包埋的示踪剂颗粒在DP3 / DP4〜2.1处具有相对均质的微环境,反映出链状聚集体构造的速度相当慢。在微观水平上,多糖网络动力学的行为似乎并不总是与整体整体宏观响应相匹配。

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