Jørgensen Tor Erik, Sletmoen Marit, Draget Kurt I, Stokke Bjørn T
NOBIPOL, Departments of Physics and Biotechnology, The Norwegian University of Science and Technology, NTNU, NO-7491 Trondheim, Norway.
Biomacromolecules. 2007 Aug;8(8):2388-97. doi: 10.1021/bm070208d. Epub 2007 Jun 28.
Structural polysaccharides of the alginate family form gels in aqueous Ca2+-containing solutions by lateral association of chain segments. The effect of adding oligomers of alpha-l-guluronic acid (G blocks) to gelling solutions of alginate was investigated using rheology and atomic force microscopy (AFM). Ca-alginate gels were prepared by in situ release of Ca2+. The gel strength increased with increasing level of calcium saturation of the alginate and decreased with increasing amount of free G blocks. The presence of free G blocks also led to an increased gelation time. The gel point and fractal dimensionalities of the gels were determined based on the rheological characterization. Without added free G blocks the fractal dimension of the gels increased from df = 2.14 to df = 2.46 when increasing [Ca2+] from 10 to 20 mM. This increase was suggested to arise from an increased junction zone multiplicity induced by the increased concentration of calcium ions. In the presence of free G blocks (G block/alginate = 1/1) the fractal dimension increased from 2.14 to 2.29 at 10 mM Ca2+, whereas there was no significant change associated with addition of G blocks at 20 mM Ca2+. These observations indicate that free G blocks are involved in calcium-mediated bonds formed between guluronic acid sequences within the polymeric alginates. Thus, the added oligoguluronate competes with the alginate chains for the calcium ions. The gels and pregel situations close to the gel point were also studied using AFM. The AFM topographs indicated that in situations of low calcium saturation microgels a few hundred nanometers in diameter develop in solution. In situations of higher calcium saturation lateral association of a number of alginate chains are occurring, giving ordered fiber-like structures. These results show that G blocks can be used as modulators of gelation kinetics as well as local network structure formation and equilibrium properties in alginate gels.
藻酸盐家族的结构多糖通过链段的侧向缔合在含Ca2+的水溶液中形成凝胶。使用流变学和原子力显微镜(AFM)研究了向藻酸盐凝胶溶液中添加α-L-古洛糖醛酸(G块)低聚物的影响。通过Ca2+的原位释放制备Ca-藻酸盐凝胶。凝胶强度随着藻酸盐钙饱和度的增加而增加,随着游离G块数量的增加而降低。游离G块的存在还导致凝胶化时间增加。基于流变学表征确定凝胶的凝胶点和分形维数。在不添加游离G块的情况下,当[Ca2+]从10 mM增加到20 mM时,凝胶的分形维数从df = 2.14增加到df = 2.46。这种增加被认为是由钙离子浓度增加引起的连接区多重性增加所致。在存在游离G块(G块/藻酸盐 = 1/1)的情况下,在10 mM Ca2+时,分形维数从2.14增加到2.29,而在20 mM Ca2+时添加G块没有显著变化。这些观察结果表明,游离G块参与了聚合藻酸盐中糖醛酸序列之间形成的钙介导键。因此,添加的低聚古洛糖醛酸与藻酸盐链竞争钙离子。还使用AFM研究了接近凝胶点的凝胶和预凝胶情况。AFM地形图表明,在低钙饱和度情况下,溶液中会形成直径几百纳米的微凝胶。在较高钙饱和度情况下,许多藻酸盐链发生侧向缔合,形成有序的纤维状结构。这些结果表明,G块可作为藻酸盐凝胶中凝胶化动力学、局部网络结构形成和平衡性质的调节剂。