Université de Toulouse, UPS, LBAE, IUT «A», 24 rue d'Embaqués, F-32000 Auch, France.
Water Res. 2013 May 15;47(8):2901-8. doi: 10.1016/j.watres.2013.03.010. Epub 2013 Mar 18.
A colorimetric assay based on the conventional anthrone reaction was investigated for specific quantification of uronic acids (UA) in the presence of neutral sugars and/or proteins. Scanning of glucose (Glu) and glucuronic acid (GlA) was performed after the reaction with anthrone and a double absorbance reading was made, at 560 nm and at 620 nm, in order to quantify the UA and neutral sugars separately. The assay was implemented on binary or ternary solutions containing Glu, GlA and bovine serum albumin (BSA) in order to validate its specificity towards sugars and check possible interference with other biochemical components such as proteins. Statistical analysis indicated that this assay provided correct quantification of uronic sugars from 50 to 400 mg/l and of neutral sugars from 20 to 80 mg/l, in the presence of proteins with concentrations reaching 600 mg/l. The proposed protocol can be of great interest for simultaneous determination of uronic and neutral sugars in complex biological samples. In particular, it can be used to correctly quantify the Extracellular Polymeric Substances (EPS) isolated from the biological matrix of many bacterial aggregates, even in the presence of EPS extractant such as EDTA.
基于传统蒽酮反应的比色法被用于在中性糖和/或蛋白质存在的情况下特异性定量检测糖醛酸(UA)。在与蒽酮反应后,对葡萄糖(Glu)和葡萄糖醛酸(GlA)进行扫描,并在 560nm 和 620nm 处进行双吸收读数,以分别定量 UA 和中性糖。该测定法用于含有 Glu、GlA 和牛血清白蛋白(BSA)的二元或三元溶液中,以验证其对糖的特异性,并检查与其他生化成分(如蛋白质)可能存在的干扰。统计分析表明,该测定法在蛋白质浓度达到 600mg/L 的情况下,能够正确定量 50-400mg/L 的糖醛酸和 20-80mg/L 的中性糖。该方案对于同时测定复杂生物样品中的糖醛酸和中性糖具有重要意义。特别是,它可以用于正确定量从许多细菌聚集体的生物基质中分离出的细胞外聚合物质(EPS),即使存在 EDTA 等 EPS 提取剂也是如此。