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通过高效液相色谱法评估甲醇解用于测定胶凝角叉菜胶和琼脂糖中的复合糖。

Assessment of methanolysis for the determination of composite sugars of gelling carrageenans and agarose by HPLC.

作者信息

Quemener B, Lahaye M, Metro F

机构信息

Institut National de la Recherche Agronomique, Laboratoire de Biochimie et Technologie des Glucides, Nantes, France.

出版信息

Carbohydr Res. 1995 Jan 3;266(1):53-64. doi: 10.1016/0008-6215(94)00249-f.

DOI:10.1016/0008-6215(94)00249-f
PMID:7697651
Abstract

The characterization of the main composite sugars of commercial gelling red algae galactans (agarose, iota and kappa carrageenans) by methanolysis and separation of the methyl glycosides produced by high performance liquid chromatography is described. The methanolysis (methanolic hydrochloric acid strength, temperature, and reaction time) was optimized in order to release monosaccharides in near quantitative yield. The results were compared to those obtained by (1) gas chromatography of the alditol acetates of the neutral sugars released by acid hydrolysis and (2) specific colorimetric determination of the acid-labile 3,6-anhydrogalactosyl residue. Conditions such as methanolic 0.125 M HCl for 1 h at 85 degrees C were sufficient to release all of the galactosidic and 3,6-anhydrogalactosidic bonds for iota carrageenan without apparent degradation of the anhydrogalactosyl unit. However, with the same conditions, the yields of 3,6-anhydrogalactosyl residues were 80 and 70% for kappa carrageenan and agarose, respectively. These yields were not improved by stronger conditions. At the opposite extreme, under very mild methanolysis conditions such as methanolic 0.01 M HCl at 100 degrees C for 1 h, agars and gelling carrageenans were well differentiated by the respective determination of agarobiose- and carrabiose-dimethyl acetal which are well-separated on octadecyl reversed phase HPLC columns with water as eluent.

摘要

描述了通过甲醇解以及高效液相色谱法分离所产生的甲基糖苷,对商业胶凝红藻半乳聚糖(琼脂糖、ι-卡拉胶和κ-卡拉胶)的主要复合糖进行表征的方法。对甲醇解条件(甲醇盐酸浓度、温度和反应时间)进行了优化,以便以接近定量的产率释放单糖。将结果与通过以下方法获得的结果进行比较:(1)对酸水解释放的中性糖的糖醇乙酸酯进行气相色谱分析,以及(2)对酸不稳定的3,6-脱水半乳糖基残基进行特定的比色测定。诸如在85℃下用0.125 M HCl甲醇溶液反应1小时的条件足以释放ι-卡拉胶的所有半乳糖苷键和3,6-脱水半乳糖苷键,而脱水半乳糖基单元没有明显降解。然而,在相同条件下,κ-卡拉胶和琼脂糖的3,6-脱水半乳糖基残基的产率分别为80%和70%。更强的条件并没有提高这些产率。在另一个极端情况下,在非常温和的甲醇解条件下,如在100℃下用0.01 M HCl甲醇溶液反应1小时,通过分别测定琼脂二糖和卡拉二糖二甲基缩醛,可以很好地区分琼脂和胶凝卡拉胶,它们在以水为洗脱剂的十八烷基反相HPLC柱上能够很好地分离。

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