Aix Marseille Univ, CNRS, LCE, Marseille, France.
Laboratoire de Biodiversité et Biotechnologies Marines, Institut National des Sciences et Technologie de la Mer, Centre La Goulette, Port de Pêche, Tunis 2060, Tunisia.
Molecules. 2021 Sep 25;26(19):5809. doi: 10.3390/molecules26195809.
This paper presents the development and the application of a multisyringe flow injection analysis system for the fluorimetric determination of the major heat-stable known allergen in shrimp, rPen a 1 (tropomyosin). This muscle protein, made up of 284 amino acids, is the main allergen in crustaceans and can be hydrolyzed by microwave in hydrochloric acid medium to produce glutamic acid, the major amino acid in the protein. Glutamic acid can then be quantified specifically by thermal conversion into pyroglutamic acid followed by chemical derivatization of the pyroglutamic acid formed by an analytical protocol based on an OPA-NAC reagent. Pyroglutamic acid can thus be quantified between 1 and 100 µM in less than 15 min with a detection limit of 1.3 µM. The method has been validated by measurements on real samples demonstrating that the response increases with the increase in the tropomyosin content or with the increase in the mass of the shrimp sample.
本文介绍了一种多注射器流动注射分析系统的开发和应用,用于荧光测定虾中主要耐热过敏原 rPen a 1(肌球蛋白)。这种由 284 个氨基酸组成的肌肉蛋白是甲壳类动物中的主要过敏原,可在盐酸介质中经微波水解产生谷氨酸,这是蛋白质中的主要氨基酸。然后,通过基于 OPA-NAC 试剂的分析方案,将谷氨酸特异性转化为焦谷氨酸,再对形成的焦谷氨酸进行化学衍生化,可定量测定 1 至 100 μM 之间的谷氨酸,检测限为 1.3 μM。该方法已通过对实际样品的测量进行了验证,结果表明,响应值随肌球蛋白含量的增加或虾样质量的增加而增加。