Degradation and interconversion of plant pteridines during sample preparation and ultra-high performance liquid chromatography-tandem mass spectrometry

被引:6
作者
Van Daele, Jeroen [1 ]
Blancquaert, Dieter [2 ]
Kiekens, Filip [1 ]
Van Der Straeten, Dominique [2 ]
Lambert, Willy E. [1 ]
Stove, Christophe P. [1 ]
机构
[1] Univ Ghent, Dept Bioanal, Lab Toxicol, B-9000 Ghent, Belgium
[2] Univ Ghent, Dept Physiol, Lab Funct Plant Biol, B-9000 Ghent, Belgium
关键词
(U)HPLC-MS/MS; Pterins; Stability; Degradation; Interconversion; Potato; Arabidopsis; ALKALINE AQUEOUS-SOLUTIONS; FOLATE BIOSYNTHESIS GENES; URINE SPECIFIC-GRAVITY; EARLY CANCER-DETECTION; ARABIDOPSIS-THALIANA; POTATO-TUBERS; FOLIC-ACID; PTERIN; RICE; HPLC;
D O I
10.1016/j.foodchem.2015.08.098
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The degradation and interconversion of a selected set of pterins (dihydroneopterin, hydroxymethyldihydropterin, diydroxanthopterin, neopterin, hydroxymethylpterin, xanthopterin, 6-formylpterin, 6-carboxypterin and pterin), spiked to charcoal-treated potato and Arabidopsis thaliana matrix was investigated, together with their relative recovery in potato and A. thaliana. As a result, a matrix-specific procedure for the ultra-high performance liquid chromatography-tandem mass spectrometry based determination of 6 aromatic pterins (neopterin, hydroxymethylpterin, xanthopterin, 6-formylpterin, 6-carboxypterin and pterin) is proposed: 1.5 ml of an N-2-flushed, alkaline (pH = 10) extraction solvent is added to 200 mg of plant sample. After boiling and homogenization, the samples are incubated: Arabidopsis samples for 30 min at room temperature, while shaking, and potato samples for 2 h at 37 degrees C (applying a dienzyme treatment with alpha-amylase and protease). After a final boiling step, the samples are ultrafiltrated and resulting extracts are analyzed by UHPLC-MS/MS. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1189 / 1198
页数:10
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