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Determination of wheat, rye and spelt authenticity in bread by targeted peptide biomarkers

机译:用靶向肽生物标志物测定小麦,黑麦和拼写真实性

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Adulteration of food and mislabeled products in global market is a major financial and reputational risk for food manufacturers and trade companies. Consequently, there is a necessity to develop analytical methods to meet these issues. An analytical strategy to check the authenticity of wheat, spelt and rye addition in bread products was developed based on database research, in silico digestion confirming peptide specificity and finally quantification by liquid chromatography-tandem mass spectrometry analysis. Peptide markers for wheat (SQQQISQQPQQLPQQQQIPQQPQQF; QQHQIPQQPQQFPQQQQF and QPHQPQQPYPQQ), spelt (ASIVVGIGGQ; SQQPGQIIPQQPQQPSPL) and rye (LPQSHKQHVGQGAL; AQVQGIIQPQQL and QQFPQQPQQSFPQQPQQPVPQQPL) were identified, verified by protein Basic Local Alignment Search Tool and database research and used for quantification in bread. The specific use of multi-reaction monitoring transitions of selected peptides permitted the identification of closely related species wheat and spelt. Other cereal species (emmer, einkorn, barley, maize, rye and oat) were also checked. The target peptides were quantified at different levels using own reference baked products (bread) after in-solution chymotryptic digestion. Sensitivity of the identification was 0.5-1% using flour-based (0-25%) matrix calibration and the analytical recovery in bread was 80-125%. The analytical strategy described here supplies an emerging, independent and flexible tool in controlling the labeling of bread. (C) 2017 Elsevier Inc. All rights reserved.
机译:全球市场食品和误标产品的掺杂是食品制造商和贸易公司的主要财务和声誉风险。因此,有必要开发分析方法以满足这些问题。基于数据库研究,开发了一种检查小麦的真实性的分析策略,在面包产品中,在硅片消化中,通过液相色谱 - 串联质谱分析进行了硅片特异性,硅质消化,并最终进行量化。小麦肽标记(SQQQISQQPQQLPQQQQIPQQPQQF; QQHQIPQQPQQFPQQQQF和QPHQPQQPYPQQ),拼(ASIVVGIGGQ; SQQPGQIIPQQPQQPSPL)和黑麦(LPQSHKQHVGQGAL; AQVQGIIQPQQL和QQFPQQPQQSFPQQPQQPVPQQPL)进行了鉴定,通过蛋白基本局部比对搜索工具和数据库研究验证,用于面包定量。多反应监测选定肽的特定用途允许鉴定密切相关的物种小麦并拼写。还检查了其他谷物(emmer,einkorn,大麦,玉米,黑麦和燕麦)。使用自己的参考烘焙产品(面包)在溶液内凋亡物质消化后在不同水平下量化靶肽。使用面粉(0-25%)基质校准鉴定的敏感性为0.5-1%,并且面包中的分析恢复为80-125%。这里描述的分析策略提供了控制面包标记的新出现,独立和灵活的工具。 (c)2017年Elsevier Inc.保留所有权利。

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