Wang Pei, Zou Min, Liu Kexin, Gu Zhenxin, Yang Runqiang
College of Food Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Food Chem. 2018 Jan 15;239:984-992. doi: 10.1016/j.foodchem.2017.07.029. Epub 2017 Jul 11.
The physicochemical properties of gliadin upon mild thermal treatment were studied in terms of polymerization behavior, conformation and viscoelasticity. Gliadin samples were heated at 40, 60 and 90°C for up to 20min. Results showed that α-gliadin started to polymerize via disulfide (SS) bonds before γ-gliadin at 90°C, resulting in the extractability loss in aqueous ethanol. β-Turn and specific β-sheet structures were partially conversed to α-helices during thermal treatment. Rearrangement of non-covalent forces might contribute to viscosity loss of gliadin at 40 and 60°C. However, the elevated elasticity at 90°C was mainly due to gliadin polymerization while the viscosity variation was resulted from combined effects of non-covalent forces and covalent SS bonds. This study could offer insight into the variation of gliadin characteristics during the early baking process.
研究了醇溶蛋白在温和热处理条件下的物理化学性质,包括聚合行为、构象和粘弹性。将醇溶蛋白样品在40、60和90°C下加热长达20分钟。结果表明,在90°C时,α-醇溶蛋白比γ-醇溶蛋白更早通过二硫键(SS)开始聚合,导致在乙醇水溶液中的可提取性丧失。在热处理过程中,β-转角和特定的β-折叠结构部分转变为α-螺旋。非共价力的重排可能导致40和60°C下醇溶蛋白的粘度降低。然而,90°C时弹性增加主要是由于醇溶蛋白聚合,而粘度变化是由非共价力和共价SS键的综合作用引起的。该研究可为烘焙初期醇溶蛋白特性的变化提供见解。