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Aging Properties of Films of Plasticized Vital Wheat Gluten Cast from Acidic and Basic Solutions

机译:酸性和碱性溶液浇铸的增塑重要小麦面筋膜的老化性能

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In order to understand the mechanisms behind the undesired aging of films based on vital wheat gluten plasticized with glycerol,films cast from water/ethanol solutions were investigated.The effect of pH was studied by casting from solutions at pH 4 and pH 11.The films were aged for 120 days at 50% relative humidity and 23 deg C,and the tensile properties and oxygen and water vapor permeabilities were measured as a function of aging time.The changes in the protein structure were determined by infrared spectroscopy and size-exclusion and reverse-phase high-performance liquid chromatography,and the film structure was revealed by optical and scanning electron microscopy.The pH 11 film was mechanically more stable with time than the pH 4 film,the latter being initially very ductile but turning brittle toward the end of the aging period.The protein solubility and infrared spectroscopy measurements indicated that the protein structure of the pH 4 film was initially significantly less polymerized/ aggregated than that of the pH 11 film.The polymerization of the pH 4 film increased during storage but it did not reach the degree of aggregation of the pH 11 film.Reverse-phase chromatography indicated that the pH 11 films were to some extent deamidated and that this increased with aging.At the same time a large fraction of the aged pH 11 film was unaffected by reducing agents,suggesting that a time-induced isopeptide cross-linking had occurred.This isopeptide formation did not,however,change the overall degree of aggregation and consequently the mechanical properties of the film.During aging,the pH 4 films lost more mass than the pH 11 films mainly due to migration of glycerol but also due to some loss of volatile mass.Scanning electron and optical microscopy showed that the pH 11 film was more uniform in thickness and that the film structure was more homogeneous than that of the pH 4 film.The oxygen permeability was also lower for the pH 11 film.The fact that the pH 4 film experienced a larger and more rapid change in its mechanical properties with time than the pH 11 film,as a consequence of a greater loss of plasticizer,was presumably due to its initial lower degree of protein aggregation/ polymerization.Consequently,the cross-link density achieved at pH 4 was too low to effectively retain volatiles and glycerol within the matrix.
机译:为了理解甘油增塑的重要小麦面筋膜的不期望老化的机理,研究了水/乙醇溶液流延的膜。通过在pH 4和pH 11的溶液流延来研究pH的影响。在50%相对湿度和23摄氏度下老化120天,测量拉伸性能以及氧和水蒸气渗透率随老化时间的变化。通过红外光谱和尺寸排阻法测定蛋白质结构的变化反相高效液相色谱,并通过光学和扫描电子显微镜显示薄膜结构。pH11薄膜在时间上比pH 4薄膜在机械上更稳定,后者最初具有很好的延展性,但最终变脆蛋白质溶解度和红外光谱测量表明,pH 4薄膜的蛋白质结构最初的聚合度明显降低。与pH 11膜相比zed /聚集.pH 4膜在储存过程中聚合增加,但未达到pH 11膜的聚集度。反相色谱表明pH 11膜在一定程度上同时,大部分老化的pH 11膜不受还原剂的影响,这表明发生了时间诱导的异肽交联。这种异肽的形成并没有改变。在老化过程中,pH 4薄膜的质量损失比pH 11薄膜大,这主要是由于甘油的迁移,也由于挥发性物质的损失。扫描电子和光学显微镜显示与pH 4膜相比,pH 11膜的厚度更均匀,膜的结构更均匀.pH 11膜的透氧性也较低。由于增塑剂的损失更大,其机械性能随时间的变化比pH 11膜发生了更大,更迅速的变化,这可能是由于其最初较低的蛋白质聚集/聚合度所致。因此,交联密度在pH 4时获得的值太低,无法有效地将挥发物和甘油保留在基质中。

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