Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous Abstract"Characterization of ambient volatile organic compounds at a landfill site in Guangzhou, South China"    Next AbstractEstablishment of a simple system to analyse the molecular interaction in the agglutination of Saccharomyces cerevisiae »

J Food Sci


Title:Discovery of Amadori-Type Conjugates in a Peptide Maillard Reaction and Their Corresponding Influence on the Formation of Pyrazines
Author(s):Zou T; Liu J; Song H; Liu Y;
Address:"Beijing Advanced Innovation Center for Food Nutrition and Human Health, Lab. of Molecular Sensory Science, Beijing Technology and Business Univ., Beijing, 100048, China"
Journal Title:J Food Sci
Year:2018
Volume:20180510
Issue:6
Page Number:1588 - 1595
DOI: 10.1111/1750-3841.14156
ISSN/ISBN:1750-3841 (Electronic) 0022-1147 (Linking)
Abstract:"Knowledge of the role of peptides in the Maillard reaction is rather limited. In this study, peptide Maillard reaction model systems were established. Volatile and nonvolatile MRPs (Maillard reaction products) were investigated by GC-O-MS and LC-MS. Carbohydrate module labeling (CAMOLA) experiments were performed to elucidate the carbon skeleton of these compounds. Results showed that the peptide reaction system generated more pyrazines than the free amino acid group. Several new Amadori-type conjugates were identified as novel Maillard reaction products that could greatly influence the formation of pyrazines. Our work suggested anew mechanism involving these Amadori-type conjugates and subsequent investigation revealed that the conjugates could be important intermediate products in the reaction between dicarbonyl and dipeptide. Our findings demonstrate anew pyrazine generation mechanism in the dipeptide Maillard reaction. PRACTICAL APPLICATION: We found that a dipeptide Maillard reaction system generated more pyrazines than a reaction system composed of free amino acids. New cross-linked peptide-sugar compounds were identified and found to impact the formation of pyrazines. The results of this study may help in the preparation of thermal reaction flavors using enzymatically hydrolyzed vegetable/animal proteins, which contain a considerable amount of peptides, as one of the major reactants"
Keywords:"Amino Acids/chemistry Gas Chromatography-Mass Spectrometry Glycation End Products, Advanced/chemistry *Maillard Reaction Peptides/*chemistry Proteins/chemistry Pyrazines/*chemistry Volatile Organic Compounds/chemistry Amadori-type conjugates Lc-q-tof-ms c;"
Notes:"MedlineZou, Tingting Liu, Jianbin Song, Huanlu Liu, Ye eng 2018/05/11 J Food Sci. 2018 Jun; 83(6):1588-1595. doi: 10.1111/1750-3841.14156. Epub 2018 May 10"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 19-12-2024