Metabolites of Key Flavor Compound 2,3,5-Trimethylpyrazine in Human Urine

被引:3
|
作者
Liang, Dong [1 ,2 ,3 ]
Dirndorfer, Sebastian [1 ]
Somoza, Veronika [1 ]
Krautwurst, Dietmar [1 ]
Lang, Roman [1 ]
Hofmann, Thomas [1 ,2 ]
机构
[1] Tech Univ Munich, Leibniz Inst Food Syst Biol, D-85354 Freising Weihenstephan, Germany
[2] Tech Univ Munich, Chair Food Chem & Mol Sensory Sci, D-85354 Freising Weihenstephan, Germany
[3] Sun Yat Sen Univ, Sch Agr, Shenzhen 518107, Peoples R China
关键词
coffee; trimethylpyrazine; trimethylpyrazine metabolite synthesis; quantitative stable-isotope-dilution-UHPLC-MS; MS analysis; human urine; MAILLARD REACTION; PYRAZINES; GLUCOSE;
D O I
10.1021/acs.jafc.2c06418
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Pyrazines are among the most important compound class conveying the odor impressions "roasty", "nutty", and "earthy". They are formed by the Maillard reaction and occur ubiquitously in heated foods. The excretion of metabolites of the key flavor odorant 2,3,5-trimethylpyrazine, abundant in the volatile fraction of roasted coffee, was investigated. Based on literature suggestions, putative phase 1 and phase 2 metabolites were synthesized, characterized by nuclear magnetic resonance and mass spectroscopy data and used as standards for targeted, quantitative analysis of coffee drinkers' urine using stable-isotope-dilution ultrahigh-performance liquid chromatography tandem mass spectroscopy (SIDA-UHPLC-MS/MS). The analysis of spot urine samples from a coffee intervention study revealed 3,6-dimethylpyrazine-2-carboxylic acid, 3,5-dimethylpyrazine-2-carboxylic acid, and 5,6-dimethylpyrazine-2-carboxylic acid were quantitatively dominating metabolites. Only negligible traces of pyrazinemethanols (3,6-dimethyl-2-pyrazinemethanol and 3,5,6-trimethylpyrazine-2-ol), glucuronides ((3,6-dimethylpyrazine-2-yl-)methyl-O-beta-D-glucuronide and (3,5-dimethylpyrazine-2-yl-)methyl-O-beta-D-glucuronide), and sulfates ((3,6-dimethylpyrazine-2-yl-)methyl-sulfate and (3,5-dimethylpyrazine-2-yl-)methyl-sulfate) were detected.
引用
收藏
页码:15134 / 15142
页数:9
相关论文
共 50 条
  • [1] Optimization of Fermentation Conditions for 2,3,5-Trimethylpyrazine Produced by Bacillus amyloliquefaciens from Daqu
    Liu, Xun
    Yang, Weijie
    Gu, Hongyi
    Bughio, Ayaz Ali
    Liu, Jun
    FERMENTATION-BASEL, 2024, 10 (02):
  • [2] SYNTHESIS AND N-15 NMR-SPECTRA OF 1-N-15-2,3,5-TRIMETHYLPYRAZINE AND 4-N-15-2,3,5-TRIMETHYLPYRAZINE AND THEIR N-OXIDES
    MAEDA, M
    SAKUMA, C
    KAWACHI, S
    TABEI, K
    KERIM, A
    KURIHARA, T
    OHTA, A
    JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 1995, 36 (01): : 85 - 92
  • [3] Mechanism of Carbon Skeleton Formation of 2,3,5-Trimethylpyrazine via a Conversion Reaction between Methylglyoxal and Glyoxal
    Jiang, Wei
    Wang, Xiaoyuan
    Ma, YunJiao
    Du, Ming
    Wu, Chao
    Xu, Xianbing
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2023, 71 (13) : 5337 - 5344
  • [4] RIFM fragrance ingredient safety assessment, 2,3,5-trimethylpyrazine, CAS registry number 14667-55-1
    Api, A. M.
    Belsito, D.
    Botelho, D.
    Bruze, M.
    Burton, G. A.
    Cancellieri, M. A.
    Chon, H.
    Dagli, M. L.
    Dekant, W.
    Deodhar, C.
    Fryer, A. D.
    Jones, L.
    Joshi, K.
    Kumar, M.
    Lapczynski, A.
    Lavelle, M.
    Lee, I.
    Liebler, D. C.
    Moustakas, H.
    Na, M.
    Penning, T. M.
    Ritacco, G.
    Romine, J.
    Sadekar, N.
    Schultz, T. W.
    Selechnik, D.
    Siddiqi, F.
    Sipes, I. G.
    Sullivan, G.
    Thakkar, Y.
    Tokura, Y.
    FOOD AND CHEMICAL TOXICOLOGY, 2023, 173
  • [5] RIFM fragrance ingredient safety assessment, 2,3,5-trimethylpyrazine, CAS registry number 14667-55-1
    Api, A. M.
    Belsito, D.
    Botelho, D.
    Bruze, M.
    Burton, G. A.
    Cancellieri, M. A.
    Chon, H.
    Dagli, M. L.
    Dekant, W.
    Deodhar, C.
    Fryer, A. D.
    Jones, L.
    Joshi, K.
    Kumar, M.
    Lapczynski, A.
    Lavelle, M.
    Lee, I.
    Liebler, D. C.
    Moustakas, H.
    Na, M.
    Penning, T. M.
    Ritacco, G.
    Romine, J.
    Sadekar, N.
    Schultz, T. W.
    Selechnik, D.
    Siddiqi, F.
    Sipes, I. G.
    Sullivan, G.
    Thakkar, Y.
    Tokura, Y.
    FOOD AND CHEMICAL TOXICOLOGY, 2023, 173
  • [6] Efficient degradation of 2,3,5-trimethylpyrazine by catalytic ozonation over MnOx supported on biochar derived from waste tea leaves
    He, Yinning
    Chen, Yi
    Li, Jinzhe
    Wang, Da
    Song, Shuang
    Dong, Feilong
    He, Zhiqiao
    CHEMICAL ENGINEERING JOURNAL, 2023, 464
  • [7] Efficient degradation of 2,3,5-trimethylpyrazine by catalytic ozonation over MnOx supported on biochar derived from waste tea leaves
    He, Yinning
    Chen, Yi
    Li, Jinzhe
    Wang, Da
    Song, Shuang
    Dong, Feilong
    He, Zhiqiao
    Chemical Engineering Journal, 2023, 464
  • [8] Mechanism of Carbon Skeleton Formation of 2,3,5-Trimethylpyrazine via a Conversion Reaction between Methylglyoxal and Glyoxal (vol 71, pg 5337, 2023)
    Jiang, Wei
    Wang, Xiaoyuan
    Ma, YunJiao
    Du, Ming
    Wu, Chao
    Xu, Xianbing
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2023, 71 (16) : 6511 - 6511
  • [9] An Alkylpyrazine Synthesis Mechanism Involving L-Threonine-3-Dehydrogenase Describes the Production of 2,5-Dimethylpyrazine and 2,3,5-Trimethylpyrazine by Bacillus subtilis
    Zhang, Lijie
    Cao, Yanli
    Tong, Jianan
    Xu, Yan
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2019, 85 (24)
  • [10] STUDIES ON THE SUGARY FLAVOR OF RAW CANE SUGAR .3. KEY COMPOUND OF THE SUGARY FLAVOR
    TOKITOMO, Y
    KOBAYASHI, A
    YAMANISHI, T
    MURAKI, S
    PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES, 1980, 56 (07): : 457 - 462