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首页> 外文期刊>Analytica chimica acta >Evaluation and optimization of high-throughput enzymatic assays for fast L-ascorbic acid quantification in fruit and vegetables
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Evaluation and optimization of high-throughput enzymatic assays for fast L-ascorbic acid quantification in fruit and vegetables

机译:评估和优化水果和蔬菜中快速L-抗坏血酸定量的高通量酶促测定

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In this paper, we compare and evaluate the applicability of three UV-VIS absorbance based assays for high-throughput quantification of ascorbic acid in horticultural products. All the methods involve the use of a common enzyme (ascorbate oxidase) in combination with a different indicator molecule. The three methods were retrieved from literature: a direct oxidase-method, an OPDA coupled oxidase-method and a PMS-method, which is commercially available. The analysis in high-throughput context involved the analysis in microplates in combination with the use of an automated liquid handling system. We checked (i) the performance factors of the selected methods on standard solutions, (ii) the applicability of the defined methods in high-throughput context, and, (iii) the accuracy of the methods on real samples using HPLC as a reference technique. The OPDA-method was found to be the most appropriate method for the quantification of ascorbic acid in high-throughput context with a linear range between 7.0 and 950 mgL~(-1) and excellent correlation parameters (slopes close to 1, intercepts close to 0, R~2 > 0.91) with the reference technique when real samples were analyzed. Finally, this method was optimized for assay cost and assay time. Hereto the enzymatic reaction was mathematically described using a model for enzyme kinetics, which was then used to calculate the optimal concentrations of ascorbate oxidase and OPDA. As a result of the modeling the amount of enzyme in the assay could be reduced with a factor 2.5 without affecting significantly the reaction time. In a last step the optimal concentrations were used for a successful validation with the HPLC-reference technique.
机译:在本文中,我们比较并评估了三种基于UV-VIS吸光度的测定方法在园艺产品中抗坏血酸高通量定量分析中的适用性。所有方法都涉及将常见的酶(抗坏血酸氧化酶)与不同的指示剂分子结合使用。从文献中检索了三种方法:直接氧化酶方法,ODPA偶联氧化酶方法和PMS方法(可商购)。高通量分析涉及在微孔板上进行分析,并结合使用自动化液体处理系统。我们检查了(i)在标准溶液中所选方法的性能因素,(ii)在高通量情况下定义的方法的适用性,以及(iii)使用HPLC作为参考技术的方法在实际样品上的准确性。发现OPDA方法是高通量背景下抗坏血酸定量的最合适方法,其线性范围为7.0至950 mgL〜(-1),相关参数极佳(斜率接近1,截距接近1)。 0,R〜2> 0.91)时采用参考技术分析真实样品。最后,针对测定成本和测定时间优化了该方法。迄今为止,使用酶动力学模型数学描述了酶促反应,然后将其用于计算抗坏血酸氧化酶和OPDA的最佳浓度。建模的结果是,测定中的酶量可以减少2.5倍,而不会显着影响反应时间。最后一步,将最佳浓度用于HPLC参考技术的成功验证。

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