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A novel enzymatic method for the measurement of lactose in lactose-free products

机译:一种用于测量乳糖产物中乳糖的新酶法

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BACKGROUND In recent years there has been a surge in the number of commercially available lactose-free variants of a wide variety of products. This presents an analytical challenge for the measurement of the residual lactose content in the presence of high levels of mono-, di-, and oligosaccharides. RESULTS In the current work, we describe the development of a novel enzymatic low-lactose determination method termed LOLAC (low lactose), which is based on an optimized glucose removal pre-treatment step followed by a sequential enzymatic assay that measures residual glucose and lactose in a single cuvette. Sensitivity was improved over existing enzymatic lactose assays through the extension of the typical glucose detection biochemical pathway to amplify the signal response. Selectivity for lactose in the presence of structurally similar oligosaccharides was provided by using a beta-galactosidase with much improved selectivity over the analytical industry standards from Aspergillus oryzae and Escherichia coli (EcLacZ), coupled with a 'creep' calculation adjustment to account for any overestimation. The resulting enzymatic method was fully characterized in terms of its linear range (2.3-113 mg per 100 g), limit of detection (LOD) (0.13 mg per 100 g), limit of quantification (LOQ) (0.44 mg per 100 g) and reproducibility (&= 3.2% coefficient of variation (CV)). A range of commercially available lactose-free samples were analyzed with spiking experiments and excellent recoveries were obtained. Lactose quantitation in lactose-free infant formula, a particularly challenging matrix, was carried out using the LOLAC method and the results compared favorably with those obtained from a United Kingdom Accreditation Service (UKAS) accredited laboratory employing quantitative high performance anion exchange chromatography - pulsed amperometric detection (HPAEC-PAD) analysis. CONCLUSION The LOLAC assay is the first reported enzymatic method that accurately quantitates lactose in lactose-free samples. (c) 2018 The Authors. Journal of The Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.
机译:背景技术近年来,在各种产品的可商购自由乳糖变种的数量上存在浪涌。这提出了在高水平的单 - ,二 - 和低聚糖存在下测量残留乳糖含量的分析挑战。结果目前的工作,我们描述了一种新的酶促酶低乳糖测定方法的发展,其称为Lolac(低乳糖),其基于优化的葡萄糖去除预处理步骤,然后是序列酶测定法测量残留葡萄糖和乳糖在单一的比色杯中。通过延伸典型的葡萄糖检测生化途径来改善现有酶乳糖测定的敏感性,以扩增信号响应。通过使用来自Aspergillus oryzae和大肠杆菌(Eclacz)的分析行业标准的β-半乳糖苷酶提供结构相似的寡糖在结构相似的寡糖中的选择性,再加上“蠕变”计算调整,以解释任何高估。得到的酶法在其线性范围(每100克2.3-113mg),检测限(LOD)(每100克0.11mg),定量限(LOQ)(每100g 0.44mg)(每100g 0.44mg)(每100g 0.44mg)的限制和再现性(& = 3.2%的变异系数(cv))。通过尖刺实验分析一系列市售的无乳糖样品,得到优异的回收率。使用Lolac方法进行乳糖婴儿配方中的乳糖定量,使用LOLAC方法进行特别具有挑战性的基质,并且结果与从英国认证服务(UKAS)获得的那些相比,获得了定量的高性能阴离子交换色谱 - 脉冲倍数检测(HPAEC-PAD)分析。结论Lolac测定是第一种预先定量无乳糖样品中乳糖的酶促方法。 (c)2018作者。 John Wiley&amp出版的粮食与农业科学杂志。 SONS LTD代表化学工业社会。

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