Bioactive Products Engineering Research Center For Gansu Distinctive Plants, Northwest Normal University, Lanzhou, China.
Int J Biol Macromol. 2012 Jun 1;50(5):1201-6. doi: 10.1016/j.ijbiomac.2012.03.009. Epub 2012 Mar 29.
It was essential to understand the chemical structure of polysaccharides for further research and biochemical or medical application of this natural biopolymer. In the present study, sulfated derivatives of guar gum with high degree of sulfation (DS) were synthesized using 4-dimethylaminopyridine (DMAP)/dimethylcyclohexylcarbodiimide (DCC) as catalyst in homogeneous conditions. The effects of the ratio of chlorosulfuric acid to pyridine, the content of catalyst and reaction temperature were investigated. Results of FT-IR, (1)H and (13)C NMR indicated that C-6 substitution was predominant in sulfated polysaccharide. In the sulfation reaction, a sharp decrease in M(W) was observed. The enhanced antioxidant activities of sulfated polysaccharides were not a function of a single factor but a combination of high DS and low molecule weight.
为了进一步研究和生物化学或医学应用这种天然生物聚合物,了解多糖的化学结构是至关重要的。在本研究中,使用 4-二甲氨基吡啶(DMAP)/二甲基环己基碳二亚胺(DCC)作为均相条件下的催化剂,合成了高度硫酸化(DS)的瓜尔胶硫酸酯衍生物。考察了氯磺酸与吡啶的比例、催化剂含量和反应温度的影响。FT-IR、(1)H 和(13)C NMR 的结果表明,C-6 取代在硫酸化多糖中占主导地位。在硫酸化反应中,观察到 M(W)急剧下降。硫酸化多糖增强的抗氧化活性不是单一因素的功能,而是高 DS 和低分子量的结合。