Literature DB >> 18318498

Formation of peptide-bound Heyns compounds.

René Krause1, Kathrin Schlegel, Evelyn Schwarzer, Thomas Henle.   

Abstract

The reaction of the Nalpha-hippuryllysine (BzGK) with fructose was investigated in two model systems to obtain an insight in fructose-induced modification of lysine in bakery products. After BzGK and fructose had been heated in a buffered low-moisture model system (80 degrees C, 60 min, aW = 0.86, pH 7.4), formation of epimeric Heyns compounds Nalpha-hippuryl-Nepsilon-glucosyl-lysine (BzGGlcK) and Nalpha-hippuryl-Nepsilon-mannosyl-lysine (BzGManK) was clearly demonstrated using RP-HPLC with UV as well as MS detection. The Amadori compound Nalpha-hippuryl-Nepsilon-fructosyl-lysine (BzGFruK) was formed in glucose-containing samples. When BzGK was added to the dough of fructose-containing biscuits, the Heyns compounds were detectable after baking at 175 degrees C for 7 min. The yields of the Heyns compounds in the fructose-containing biscuits and the yield of the Amadori compound in the glucose-containing biscuits were determined to 33 and 63%, pointing to the fact that formation of substantial amounts of Heyns products is very likely in fructose-containing bakery products.

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Year:  2008        PMID: 18318498     DOI: 10.1021/jf073256y

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


  2 in total

1.  Solid-phase synthesis of D-fructose-derived Heyns peptides utilizing Nα-Fmoc-Lysin[Nε-(2-deoxy-D-glucos-2-yl),Nε-Boc]-OH as building block.

Authors:  Sebastian Schmutzler; Daniel Knappe; Andreas Marx; Ralf Hoffmann
Journal:  Amino Acids       Date:  2021-05-02       Impact factor: 3.520

2.  Chromatographic separation of glycated peptide isomers derived from glucose and fructose.

Authors:  Sebastian Schmutzler; Ralf Hoffmann
Journal:  Anal Bioanal Chem       Date:  2022-08-03       Impact factor: 4.478

  2 in total

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