4.7 Article

Studies on the Formation of Maillard and Caramelization Products from Glucosamine Incubated at 37 °C

期刊

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
卷 63, 期 27, 页码 6249-6261

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jafc.5b02664

关键词

glucosamine; Heyns compound; Maillard reaction; alpha-dicarbonyl compounds (alpha-DCs); o-phenylenediamine (OPD); fructosazine

资金

  1. Alberta Innovates-Bio Solutions (Al Bio)
  2. ALMA
  3. Natural Sciences and Engineering Research Council (NSERC) of Canada

向作者/读者索取更多资源

This experiment compared the in vitro degradation of glucosamine (GlcN), N-acetylglucosamine, and glucose in the presence of NH3 incubated at 37 degrees C in phosphate buffer from 0.5 to 12 days. The reactions were monitored with UV-vis absorption and fluorescence emission spectroscopies, and the main products of degradation, quinoxaline derivatives of alpha-dicarbonyl compounds and condensation products, were determined using UHPLC-UV and Orbitrap mass spectrometry. GlcN produced two major dicarbonyl compounds, glucosone and 3-deoxyglucosone, ranging from 709 to 3245 mg/kg GlcN and from 272 to 4535 mg/kg GlcN, respectively. 3,4-Dideoxyglucosone-3-ene, glyoxal, hydroxypyruvaldehyde, methylglyoxal, and diacetyl were also detected in lower amounts compared to glucosone and 3-deoxyglucosone. Several pyrazine condensation products resulting from the reaction between dicarbonyls and GlcN were also identified. This study determined that GlcN is a significantly unstable molecule producing a high level of degradation products at 37 degrees C.

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