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通过液相色谱和离子喷雾串联质谱法测定1-氨基环丙烷-1-羧酸及其结构类似物

Determination of 1-aminocyclopropane-1-carboxylic acid and its structural analogue by liquid chromatography and ion spray tandem mass spectrometry.

作者信息

Petritis K, Dourtoglou V, Elfakir C, Dreux M

机构信息

Institut de Chimie Organique et Analytique, CNRS UPRES-A, Université d'Orléans, France.

出版信息

J Chromatogr A. 2000 Oct 27;896(1-2):335-41. doi: 10.1016/s0021-9673(00)00757-3.

Abstract

Liquid chromatography coupled to ion spray tandem mass spectrometry was developed as a method for the simultaneous analysis of the amino acid 1-aminocyclopropane-1-carboxylic acid (ACC) and its structural analogue, cyclopropane-1,1-dicarboxylic acid (CDA). ACC and CDA fragmentation as well as optimization of MS parameters were investigated in positive ion mode. In selective reaction monitoring mode the protonated molecule [M+H]+ was selected as parent ion for both ACC and CDA, while the immonium ion from ACC and the [M+H-H2O]+ ion from CDA were selected, respectively, as product ions. In spite of the high selectivity of MS/MS among the 20 protein amino acids potentially present with ACC and CDA in the plant material analyzed, Glu and Thr can interfere with the signal of ACC. As a result, their chromatographic separation is necessary. This was achieved in less than 4 min by ion-pair reversed-phase chromatography with nonafluoropentanoic acid as ion-pair reagent. A linear response within a concentration range of 1-5 mg l(-1) was observed for this LC method and the detection limit was found to be 20 pmol for ACC and 150 pmol for CDA (using a 20-microl loop). This methodology was successfully applied to the detection of ACC in apple tissue.

摘要

液相色谱-离子喷雾串联质谱联用技术被开发为一种同时分析氨基酸1-氨基环丙烷-1-羧酸(ACC)及其结构类似物环丙烷-1,1-二羧酸(CDA)的方法。在正离子模式下研究了ACC和CDA的碎片化以及质谱参数的优化。在选择反应监测模式下,质子化分子[M+H]+被选为ACC和CDA的母离子,而来自ACC的铵离子和来自CDA的[M+H-H2O]+离子分别被选为产物离子。尽管在分析的植物材料中可能与ACC和CDA同时存在的20种蛋白质氨基酸之间,MS/MS具有高选择性,但Glu和Thr会干扰ACC的信号。因此,它们的色谱分离是必要的。通过以九氟戊酸为离子对试剂的离子对反相色谱法,在不到4分钟内实现了分离。该液相色谱方法在1-5 mg l(-1)的浓度范围内观察到线性响应,ACC的检测限为20 pmol,CDA的检测限为150 pmol(使用20微升定量环)。该方法成功应用于苹果组织中ACC的检测。

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