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Sulfation of citrus pectin by pyridine-sulfurtrioxide complex and its anticoagulant activity

机译:吡啶-三氧化硫配合物对柑桔果胶的硫酸化及其抗凝活性

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Citrus pectin (CP) was sulfated by the pyridine sulfur-trioxide complex in dimethyl sulfoxide (DMSO). Monosaccharide composition analysis revealed a decrease in the GalA content after sulfation. A decrease in the average molecular weight (MW) and a fall in particle size of the pectin gave additional proof of pectin degradation during the sulfation reaction. Structural characterization by IR and NMR spectra indicated sulfation occurred mainly at positions C-2, C-3 of the GalA (located in backbone region of the CP). Anticoagulant assays demonstrated that sulfated CP (TBA-3) could prolong activated partial thromboplastin time and thrombin time, with an activity of 51.96 IU/mg and 15.2 IU/mg, respectively. Further investigation on coagulation factors indicated TBA-3 could achieve inactivation of thrombin with both heparin cofactor II and antithrombin. Our results indicated sulfated pectin might be a promising anticoagulant ingredient with excellent activity and simple monosaccharides, and could be a possible substitute for the limited heparin. (C) 2014 Elsevier Ltd. All rights reserved.
机译:在二甲基亚砜(DMSO)中,吡啶三氧化硫复合物将柑橘果胶(CP)硫酸盐化。单糖组成分析显示硫酸化后GalA含量降低。果胶的平均分子量(MW)的降低和果胶粒径的降低提供了在硫酸化反应期间果胶降解的额外证据。通过IR和NMR光谱的结构表征表明硫酸化主要发生在GalA的C-2,C-3位置(位于CP的骨架区域)。抗凝试验表明,硫酸CP(TBA-3)可以延长活化的部分凝血活酶时间和凝血酶时间,其活性分别为51.96 IU / mg和15.2 IU / mg。对凝血因子的进一步研究表明,TBA-3可以通过肝素辅因子II和抗凝血酶实现凝血酶的灭活。我们的结果表明,硫酸果胶可能是一种很有前途的抗凝成分,具有出色的活性和简单的单糖,并且可能会替代有限的肝素。 (C)2014 Elsevier Ltd.保留所有权利。

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