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A fast and accurate UPLC method for analysis of proteinogenic amino acids.

机译:一种快速,准确的UPLC方法,用于分析蛋白原氨基酸。

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摘要

A reliable and inexpensive method for the measurement of proteinogenic amino acids was developed. It allows the screening of large sample volumes that is important for current food and feed applications, but also for future biobased applications. The method is based on acid hydrolysis and automated pre-column derivatision in the injection needle of the autosampler using o-phthalaldehyde/ethanethiol reagent in combination with 9-fluorenylmethyl chloroformate. The calculated mean limit of detection and limit of quantification of pure amino acids were 2.3 and 4.6 muM, respectively. With this method, it was possible to accurately analyse the amino acid composition of bovine serum albumin, soy meal, Jatropha press cake, and cyanophycin. Mean reproducibility of all amino acids from bovine serum albumin was 6.8 %, with a mean recovery of 95 %. The sample run time is 16 min with a total cycle time from injection to injection of an acid hydrolyzed sample of 22 min, resulting in a greener method due to a reduction in solvent consumption. copyright Springer Science+Business Media New York 2013.
机译:开发了一种可靠且廉价的蛋白质原氨基酸测量方法。它可以筛查大量样品,这对于当前的食品和饲料应用以及未来的生物基应用都很重要。该方法基于酸水解和自动进样器在进样针中的自动柱前衍生化,该方法使用邻苯二甲醛/乙硫醇试剂与9-芴基甲基氯甲酸酯联用。计算得出的平均检测极限和纯氨基酸定量极限分别为2.3和4.6μM。通过这种方法,可以准确地分析牛血清白蛋白,豆粕,麻风树压滤饼和蓝霉素的氨基酸组成。牛血清白蛋白中所有氨基酸的平均重现性为6.8%,平均回收率为95%。样品运行时间为16分钟,从注入到注入酸水解样品的总循环时间为22分钟,由于减少了溶剂消耗,因此方法更环保。版权所有Springer Science + Business Media纽约,2013年。

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