Literature DB >> 34968913

Unravelling caramelization and Maillard reactions in glucose and glucose + leucine model cakes: Formation and degradation kinetics of precursors, α-dicarbonyl intermediates and furanic compounds during baking.

J Lee1, S Roux2, E Le Roux3, S Keller4, B Rega5, C Bonazzi6.   

Abstract

Understanding the mechanisms leading to the multitude of newly-formed compounds generated during the thermal processing of food is important for the reasoned construction of quality. Thanks to a solid food model with a structure and technological history comparable to that of a real sponge cake and containing only known amounts of precursors (glucose with or without leucine), an adapted reaction scheme unravelling Maillard and caramelization reactions was built and then compared to experimental kinetic data measured on numerous reaction markers (precursors, α-dicarbonyl intermediates and furanic compounds). For caramelization, this study showed that glucose mainly formed 1,2-enediol and then fructose rather than glucosone and glyoxal. 5-hydroxymethylfurfural started to form when there were sufficient quantities of fructose, and 3,4-dideoxyoglucosone was not generated until after this step. Furfural was mainly formed via 3-deoxyglucosone. The involvement of leucine tended to accelerate the breakdown of sugars as more degradation pathways (via enaminols) were added.
Copyright © 2021 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  1deoxyglucosone (PubChem CID: 11228966, IUPAC name: (4R,5R)4,5,6trihydroxyhexane2,3dione); 3,4dideoxyglucosone (PubChem CID: 132520491, IUPAC name: (5R)5,6dihydroxy2oxohexanal); 3deoxyglucosone (PubChem CID: 114839, IUPAC name: (4S,5R)4,5,6trihydroxy2oxohexanal); 5-Hydroxymethylfurfural; 5hydroxymethylfurfural (PubChem CID: 237332, IUPAC name: 5(hydroxymethyl)furan2carbaldehyde); Deoxyglucosone; Diacetyl (PubChem CID: 650, IUPAC name: Butane2,3dione); Fructose (PubChem CID: 2723872); Furfual (PubChem CID: 7362, IUPAC name: furan2carbaldehyde); Furfural; Glucose (PubChem CID: 107526); Glucosone (PubChem CID: 159630, IUPAC name: (4S,5R)4,5,6trihydroxy2oxohexanal); Glyoxal (PubChem CID: 7860, IUPAC name: oxaldehyde); Heat transfer; Leucine (PubChem CID: 6106); Methylglyoxal (PubChem CID: 880, IUPAC name: 2oxopropanal); Reaction pathways

Year:  2021        PMID: 34968913     DOI: 10.1016/j.foodchem.2021.131917

Source DB:  PubMed          Journal:  Food Chem        ISSN: 0308-8146            Impact factor:   7.514


  1 in total

1.  Development of Innovative Candied Chestnuts from Three Chestnut Cultivars Grown in Portugal.

Authors:  Laure Foucher; Maria João Barroca; Yuliya Dulyanska; Paula M R Correia; Raquel P F Guiné
Journal:  Foods       Date:  2022-03-23
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.