共查询到19条相似文献,搜索用时 125 毫秒
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芥末等8种食物过敏原的多重PCR检测技术 总被引:1,自引:0,他引:1
依据芥末Sin a I基因、羽扇豆核糖体内转录间隔区(ITS)基因、胡桃Jug r 2基因、榛果Oleosin基因、芹菜Mtd基因、杏仁Pru du 1基因、燕麦Avenin基因和芝麻2S albumin mRNA基因设计的特异性引物序列,在普通PCR方法的基础上,通过2组4重PCR扩增,建立了同时检测芹菜、杏仁、燕麦、芝麻、芥末、羽扇豆、胡桃和榛果等8种食物过敏原的方法。该方法特异性强,灵敏性高,可应用于食品中多种食物过敏原的快速检测和监控。 相似文献
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脂肪作为食品的常见成分,会与牛乳过敏原蛋白之间发生相互作用从而影响过敏原蛋白的提取效果和检测准确性。然而,有关高脂肪型复杂食物基质的脱脂方法仍鲜有研究。以含有牛乳过敏原的巧克力模拟高脂肪型复杂基质,分别测定了正己烷、异丙醇、乙酸乙酯和脂肪酶脱脂处理后模拟基质的脱脂率和蛋白损失率,比较了脱脂前后蛋白结构、粒度、脂肪分布和微观结构的变化,同时利用间接ELISA测定脱脂前后从模拟基质中主要牛乳过敏原的含量。结果表明:正己烷的脱脂率最高且蛋白损失率最低,分别为87.87%和6.86%;脱脂会改变蛋白质的空间结构,整体由紧凑变为松散,其中正己烷组和乙酸乙酯组的变化较小。粒径在脱脂后略微降低,但异丙醇处理会使蛋白聚集成较大的颗粒,粒径由297.9nm升高至445.1nm。正己烷和乙酸乙酯脱脂后模拟基质的脂肪分布更为均一且液滴变小,表面形貌由致密光滑的块状变为疏松多孔结构;而异丙醇组和脂肪酶组仍然存在部分结块。间接ELISA结果表明:酪蛋白在乙酸乙酯组中的提取率提升了61.02%;α-乳白蛋白和β-乳球蛋白在正己烷处理后的提取质量浓度最高,分别为0.73mg/mL和1.89mg/mL。正己烷脱脂处理可以明显改善高脂肪复杂基质中过敏原的提取效果,希望研究结果可为实现高脂肪型复杂食物基质中过敏原的准确检测提供参考。 相似文献
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M. Prado I. Ortea S. Vial J. Rivas P. Calo-Mata J. Barros-Velázquez 《Critical reviews in food science and nutrition》2016,56(15):2511-2542
Currently, food allergies are an important health concern worldwide. The presence of undeclared allergenic ingredients or the presence of traces of allergens due to contamination during food processing poses a great health risk to sensitized individuals. Therefore, reliable analytical methods are required to detect and identify allergenic ingredients in food products. The present review addresses the recent developments regarding the application of DNA- and protein-based methods for the detection of allergenic ingredients in foods. The fitness-for-purpose of reviewed methodology will be discussed, and future trends will be highlighted. Special attention will be given to the evaluation of the potential of newly developed and promising technologies that can improve the detection and identification of allergenic ingredients in foods, such as the use of biosensors and/or nanomaterials to improve detection limits, specificity, ease of use, or to reduce the time of analysis. Such rapid food allergen test methods are required to facilitate the reliable detection of allergenic ingredients by control laboratories, to give the food industry the means to easily determine whether its product has been subjected to cross-contamination and, simultaneously, to identify how and when this cross-contamination occurred. 相似文献
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Hsiao‐Wei Wen Wlodzimierz Borejsza‐Wysocki Thomas R. DeCory Richard A. Durst 《Comprehensive Reviews in Food Science and Food Safety》2007,6(2):47-58
ABSTRACT: Attention to peanut allergy has been rising rapidly for the last 5 y, because it accounts for the majority of severe food‐related anaphylaxis, it tends to appear early in life, and it usually is not resolved. Low milligram amounts of peanut allergens can induce severe allergic reactions in highly sensitized individuals, and no cure is available for peanut allergy. This review presents updated information on peanut allergy, peanut allergens (Ara h1 to h8), and available methods for detecting peanuts in foods. These methods are based on the detection of either peanut proteins or a specific DNA fragment of peanut allergens. A summary of published methods for detecting peanut in foods is given with a comparison of assay formats, target analyte, and assay sensitivity. Moreover, a summary of the current availability of commercial peanut allergen kits is presented with information about assay format, target analyte, sensitivity, testing time, company/kit name, and AOAC validation. 相似文献
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食品安全是人类健康的重要保障与前提。因此,建立食品病原微生物的快速检测方法对于食品安全及人类健康有着重要的意义。简要的综述食品微生物快速检测技术的研究进展。 相似文献
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Rita C. Alves M. Fátima Barroso María Begoña González-García M. Beatriz P.P. Oliveira Cristina Delerue-Matos 《Critical reviews in food science and nutrition》2016,56(14):2304-2319
Food allergens are a real threat to sensitized individuals. Although food labeling is crucial to provide information to consumers with food allergies, accidental exposure to allergenic proteins may result from undeclared allergenic substances by means of food adulteration, fraud or uncontrolled cross-contamination. Allergens detection in foodstuffs can be a very hard task, due to their presence usually in trace amounts, together with the natural interference of the matrix. Methods for allergens analysis can be mainly divided in two large groups: the immunological assays and the DNA-based ones. Mass spectrometry has also been used as a confirmatory tool. Recently, biosensors appeared as innovative, sensitive, selective, environmentally friendly, cheaper and fast techniques (especially when automated and/or miniaturized), able to effectively replace the classical methodologies. In this review, we present the advances in the field of food allergens detection toward the biosensing strategies and discuss the challenges and future perspectives of this technology. 相似文献
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Xuli Wu Yao Li Bo Liu Yue Feng Weiyi He Zhigang Liu Lizhong Liu Zimei Wang Haizhen Huang 《Food Analytical Methods》2016,9(3):582-588
Bovine protein β-lactoglobulin (βLG) and peanut protein Ara h1 are considered good targets for detecting milk and peanut allergen, respectively. We used surface plasmon resonance (SPR) to detect βLG and Ara h1 by immobilizing the affinity-purified monoclonal antibodies on the biosensor chip. Proteins that bound to the antibody surface were detected by a shift in resonance angle. Adding polyclonal antibodies in the sandwich assay enhanced the sensitivity. βLG and Ara h1 were detected at 5.54 and 0.77 ng/mL, respectively, by SPR, and the results demonstrated good linear relation with relatively low concentrations of protein. The limit of detection with SPR was comparable to that with sandwich enzyme-linked immunosorbent assay (S-ELISA) with the same polyclonal and monoclonal antibodies. Use of the SPR biosensor is a simple, fast, and reliable way to detect βLG and Ara h1. 相似文献