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应用基于 DNA 和免疫化学方法的商业试剂盒检测泡菜及其成分中的虾过敏原。

Application of commercial kits using DNA-based and immunochemical methods for determination of shrimp allergens in kimchi and its ingredients.

机构信息

Research and Development Division, World Institute of Kimchi, Gwangju, 61755, Republic of Korea.

出版信息

J Food Sci. 2020 Oct;85(10):3638-3643. doi: 10.1111/1750-3841.15320. Epub 2020 Aug 27.

Abstract

Shrimps cause a significant part of crustacea-related allergies. It is used in processed foods, including fermented Korean foods, such as kimchi. Even low amounts of shrimp allergens can provoke reactions in consumers allergic to shrimp. Accurate food labeling is the most effective means of preventing the consumption of allergenic ingredients. To validate labeling compliance and minimize the risk of cross-contaminations, the effectiveness of methodologies used for the detection of allergens in foods should be compared. Here, seven commercial kits, based on quantitative real-time polymerase chain reaction (PCR) or enzyme-linked immunosorbent assay (ELISA), were assessed for their ability to detect the presence of shrimp allergens in food. Our results showed that SureFood real-time PCR kit and Ridascreen ELISA kit had the highest recovery, whereas five other kits underperformed in the determination of allergen content of kimchi and its ingredients. The variation in recovery among the kits depended on the limit of detection and reactivity to the shrimp allergens, tropomyosin, and sarcoplasmic calcium-binding protein. PRACTICAL APPLICATION: This research confirms the performance of commercial kits to detect the presence of shrimp allergens in kimchi, and demonstrates that the sensitivity of these kits depends on reactivity to the specific shrimp allergenic proteins. These results can be used to food allergy labeling and can be applied by the food industry to develop allergen test kits for fermented foods with improved performance.

摘要

虾是导致甲壳类相关过敏的主要原因之一。它被用于加工食品中,包括发酵的韩国食品,如泡菜。即使是低量的虾过敏原也会引起对虾过敏的消费者的反应。准确的食品标签是预防食用过敏原成分的最有效手段。为了验证标签的合规性并最大程度地减少交叉污染的风险,应比较用于检测食品中过敏原的方法的有效性。在这里,评估了七种基于定量实时聚合酶链反应 (PCR) 或酶联免疫吸附测定 (ELISA) 的商业试剂盒,以评估它们在检测食品中虾过敏原存在方面的能力。我们的结果表明,SureFood real-time PCR 试剂盒和 Ridascreen ELISA 试剂盒具有最高的回收率,而其他五个试剂盒在确定泡菜及其成分中的过敏原含量方面表现不佳。试剂盒之间回收率的差异取决于检测限和对虾过敏原、肌球蛋白和肌浆钙结合蛋白的反应性。实际应用:本研究证实了商业试剂盒在检测泡菜中虾过敏原存在方面的性能,并表明这些试剂盒的灵敏度取决于对特定虾过敏原蛋白的反应性。这些结果可用于食品过敏标签,并可由食品行业应用于开发具有改进性能的发酵食品过敏原检测试剂盒。

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