Literature DB >> 23796138

Formation of 4(5)-methylimidazole and its precursors, α-dicarbonyl compounds, in Maillard model systems.

Hae Won Jang1, Yaping Jiang, Matt Hengel, Takayuki Shibamoto.   

Abstract

Glyoxal, methylglyoxal, and diacetyl formed from sucrose alone and from a D-glucose/ammonia Maillard model system were analyzed by gas chromatography. They are known as precursors of 4(5)-methylimidazole (MI). Glyoxal and methylglyoxal formed more in acidic conditions than in basic conditions, whereas diacetyl formed the most at the highest basic condition of pH 12. Glyoxal formation from sucrose ranged from 0.33 to 32.90 μg/g under four different time and temperature conditions. Amounts of glyoxal, methylglyoxal, and diacetyl formed in Maillard model systems ranged from 2.98 to 46.12 μg/mL, from 8.27 to 156.61 μg/mL, and from 14.94 to 1588.45 μg/mL, respectively. 4(5)-MI formation in the same model systems ranged from 28.56 to 1269.71 μg/mL. Addition of sodium sulfite reduced formation of these chemicals significantly. Total α-dicarbonyl compounds in 12 commercial soft drinks ranged from 5.75 to 50.72 μg/mL. 4(5)-MI was found in levels ranging from 1.76 to 28.11 ng/mL in 10 commercial soft drinks.

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Year:  2013        PMID: 23796138     DOI: 10.1021/jf401958w

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  1 in total

1.  Formation and metabolism of 6-(1-acetol)-8-(1-acetol)-rutin in foods and in vivo, and their cytotoxicity.

Authors:  Min Chen; Pengzhan Liu; Hua Zhou; Caihuan Huang; Weiye Zhai; Yuantao Xiao; Juanying Ou; Jun He; Hani El-Nezami; Jie Zheng
Journal:  Front Nutr       Date:  2022-08-02
  1 in total

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