Zhang Hongbin, Nishinari Katsuyoshi, Williams Martin A K, Foster Tim J, Norton Ian T
College of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, People's Republic of China.
Int J Biol Macromol. 2002 Mar 8;30(1):7-16. doi: 10.1016/s0141-8130(01)00187-8.
The gelation of aqueous suspensions of the polysaccharide curdlan has been studied by dynamic rheological measurements, differential scanning calorimetry, and low-resolution time-domain 1H-NMR. Gel formation from several samples, each originating from a curdlan fraction of differing molecular weight, has been observed in order to further clarify the nature of observed phenomena by monitoring their dependence on degree of polymerisation. The results from the complementary techniques described here, in addition to those in existing literature, both for curdlan and for other ss-(1,3) glucans, have been used to build up a consistent framework for the interpretation of results. Broadly, this involves the plasticisation and dissolution of dried material on heating, the time-dependent annealing of native (as biosynthesised) structures, and the trapping of imperfectly formed pseudo-equilibrium states on re-cooling, in concert with the creation of microfibrils and network formation.
通过动态流变学测量、差示扫描量热法和低分辨率时域1H-NMR研究了多糖凝胶多糖水悬浮液的凝胶化过程。观察了几个样品的凝胶形成,每个样品都来自不同分子量的凝胶多糖级分,以便通过监测它们对聚合度的依赖性来进一步阐明所观察到的现象的性质。除了现有文献中关于凝胶多糖和其他β-(1,3)葡聚糖的结果外,这里描述的互补技术的结果已被用于建立一个一致的框架来解释结果。概括地说,这涉及加热时干燥材料的增塑和溶解、天然(生物合成)结构的时间依赖性退火,以及重新冷却时捕获不完全形成的准平衡状态,同时形成微纤维和网络。