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牛奶和含牛奶饮料中蛋氨酸亚砜的定量分析——通过厌氧酶解最小化人为氧化。

Quantitation of Methionine Sulfoxide in Milk and Milk-Based Beverages-Minimizing Artificial Oxidation by Anaerobic Enzymatic Hydrolysis.

机构信息

Chair of Food Chemistry , Technische Universität Dresden , D-01062 Dresden , Germany.

出版信息

J Agric Food Chem. 2019 Aug 14;67(32):8967-8976. doi: 10.1021/acs.jafc.9b03605. Epub 2019 Aug 1.

Abstract

Protein oxidation in milk products may entail flavor changes through reactions at methionine residues. However, little is known about the extent of methionine oxidation in milk and milk products. In the present study, a method for quantitation of methionine, methionine sulfoxide, and methionine sulfone by a stable isotope dilution assay using HILIC-ESI-MS/MS was established. For the quantitation of protein-bound analytes, anaerobic enzymatic hydrolysis was optimized to suppress artificial methionine oxidation. Moreover, the method allowed for monitoring of artificial oxidation by coincubation of the labeled probe [H]methionine. The percentage of oxidized methionine was low in UHT milk (up to 1.6%) and evaporated milk (up to 8.8%), but higher in beverages such as cocoa milk drinks (up to 19.0%) and coffee milk drinks (up to 32.8%), resulting in methionine sulfoxide concentrations of up to 6.7 g/kg protein in the latter. These products are important dietary sources of methionine sulfoxide. Model studies revealed that methionine residues can be oxidized strongly in the presence of phenolic compounds such as catechin, caffeic acid, and gallic acid, which are present in cocoa and coffee and may account for the high extent of oxidation in commercial samples.

摘要

乳制品中的蛋白质氧化可能会通过蛋氨酸残基的反应导致风味发生变化。然而,对于乳制品中蛋氨酸氧化的程度知之甚少。在本研究中,建立了一种使用 HILIC-ESI-MS/MS 通过稳定同位素稀释分析定量测定蛋氨酸、蛋氨酸亚砜和蛋氨酸砜的方法。为了定量测定蛋白质结合的分析物,优化了厌氧酶解以抑制人工蛋氨酸氧化。此外,该方法允许通过标记探针 [H]蛋氨酸的共孵育来监测人工氧化。超高温处理(UHT)牛奶(高达 1.6%)和蒸发奶(高达 8.8%)中的氧化蛋氨酸百分比较低,但在可可奶饮料(高达 19.0%)和咖啡奶饮料(高达 32.8%)等饮料中较高,导致后者中蛋白质的蛋氨酸亚砜浓度高达 6.7 g/kg。这些产品是蛋氨酸亚砜的重要膳食来源。模型研究表明,在可可和咖啡中存在的儿茶素、咖啡酸和没食子酸等酚类化合物的存在下,蛋氨酸残基可以强烈氧化,这可能解释了商业样品中高氧化程度的原因。

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