Nδ-(5-hydroxy-4,6-dimethylpyrimidine-2-yl)-L-ornithine, a novel methylglyoxal-arginine modification in beer

被引:22
作者
Glomb, MA
Rösch, D
Nagaraj, RH
机构
[1] Tech Univ Berlin, Inst Food Chem, D-13355 Berlin, Germany
[2] Univ Hosp Cleveland, Dept Ophthalmol, Ctr Vis Res, Cleveland, OH USA
关键词
N-delta-(5-Hydroxy-4,6-dimethylpyrimidine-2-yl)-L-ornithine; argpyrimidine; 5-deoxypentose; 5-deoxy-D-ribose; Maillard reaction; beer; amino acid modification;
D O I
10.1021/jf000493r
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
N-delta-(5-Hydroxy-4,6-dimethylpyrimidine-2-yl)-L-ornithine, or Argpyrimidine, was identified and quantified in beer by high-performance liquid chromatography (HPLC) and coupled gas chromatography-mass spectrometry (HRGC-MS). This novel fluorescent arginine Maillard modification represents the first amino acid modification reported in beer retaining the full backbone of the original amino acid. Two mechanisms of formation could be verified: the major pathway via methylglyoxal and the minor pathway via 5-deoxypentoses. Argpyrimidine concentrations, determined in 35 lager-type beer varieties, reached up to 27 nmol/L and could be positively correlated to beer color and wort content. Within this context, 5-deoxy-D-ribose was identified as a novel intermediate of the Maillard reaction of maltose by HRGC-MS and independent synthesis.
引用
收藏
页码:366 / 372
页数:7
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