Document Detail


The peptide-catalyzed Maillard reaction: characterization of 13C reductones.
MedLine Citation:
PMID:  18448823     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The reaction pathways of amino acids and reducing sugars are now fully understood. The focus in the last few years, however, has turned to the reaction of peptides and proteins with reducing sugars. We have investigated the reaction of gamma-aminobutanoic acid, the heptapeptide Nalpha-Acetyl-Lys-Lys-beta-Ala-Lys-beta-Ala-Lys-Gly, and the model protein beta-casein in Maillard reactions with 1-13C arabinose. Characterization of 13C-labeled acetic acid and norfuraneol by gas chromatography-mass spectrometry and nuclear magnetic resonance revealed new formation pathways. The results demonstrate significant differences in the labeling pattern of the products depending on the amine used, indicating different formation pathways of acetic acid and norfuraneol.
Authors:
Leif Alexander Garbe; Alexander Würtz; Christian T Piechotta; Roland Tressl
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Annals of the New York Academy of Sciences     Volume:  1126     ISSN:  0077-8923     ISO Abbreviation:  Ann. N. Y. Acad. Sci.     Publication Date:  2008 Apr 
Date Detail:
Created Date:  2008-05-01     Completed Date:  2008-08-12     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7506858     Medline TA:  Ann N Y Acad Sci     Country:  United States    
Other Details:
Languages:  eng     Pagination:  244-7     Citation Subset:  IM    
Affiliation:
Technische Universität Berlin, Molecular Analysis, Berlin, Germany. leif-a.garbe@tu-berlin.de
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MeSH Terms
Descriptor/Qualifier:
Amines / chemistry
Carbon Isotopes
Maillard Reaction*
Mass Spectrometry
Oligopeptides / chemical synthesis,  chemistry
Organic Chemicals / chemistry
Oxidation-Reduction
Peptides / chemistry*
gamma-Aminobutyric Acid / chemistry
Chemical
Reg. No./Substance:
0/Amines; 0/Carbon Isotopes; 0/Oligopeptides; 0/Organic Chemicals; 0/Peptides; 56-12-2/gamma-Aminobutyric Acid

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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