Zugriffsnummer 39726
Dokumenttyp Zeitschriftenartikel
Peer Review unbekannt
Sprache Englisch
Titel Structural characterization of melanoidin formed from D-glucose and L-alanine at different temperatures applying FTIR, NMR, EPR, and MALDI-ToF-MS
Autor(in); Institution
Mohsin, Ghassan Faisal; Institut für Lebensmitteltechnologie und Lebensmittelchemie, Fachgruppe Lebensmittelchemie und Analytik, Technische Universität Berlin, Berlin, GERMANY
Schmitt, Franz-Josef; Institut für Chemie, Max-Volmer-Labor für Biophysikalische Chemie, Technische Universität Berlin, Berlin, GERMANY
Kanzler, Clemens; Institut für Lebensmitteltechnologie und Lebensmittelchemie, Fachgruppe Lebensmittelchemie und Analytik, Technische Universität Berlin, Berlin, GERMANY
Epping, Jan Dirk; Institut für Chemie, Fachgruppe Anorganische und Analytische Chemie, Technische Universität Berlin, Berlin, GERMANY
Flemig, Sabine; BAM Bundesanstalt für Materialforschung und -prüfung, Berlin, GERMANY
Hornemann, Andrea; 7.2, Kryophysik und Spektrometrie, PTB-Berlin
Quelle/Jahr Food Chemistry: 245 (2018), 4, 761 - 767
ISSN 0308-8146 (PRINT) ; 1873-7072 (ONLINE)
DOI
Verlag Amsterdam [u.a.]: Elsevier
Freie Schlagworte Melanoidin ; Maillard reaction ; FTIR spectroscopy ; EPR spectroscopy ; NMR spectroscopy ; MALDI- ToF-MS ; b-glucose ; L-alanine
Zusammenfassung The aim of this study was to identify specific chemical bonds and characteristic structures in melanoidins formed from D-glucose and L-alanine between 130 and 200 °C. The results might be used to control the type and amount of melanoidin produced during food processing. For this purpose, complementary techniques, such as FTIR, NMR, EPR, and  ALDI-ToF, were employed. At 160 °C color, solubility and UV/Vis absorption change characteristically and consequently, structural transformations could be observed in FTIR and NMR spectra. For example, sharp signals of N-H, C-N, and C-H oscillations in the L-alanine spectrum are prone to inhomogeneous broadening in melanoidins prepared above 150 °C. These changes are caused due to formation of heterogeneous macromolecular structures and occur during condensation reactions that lead to an increasing loss of water from the melanoidins with increasing temperatures. Additionally, MALDI-ToF-MS indicates the polymerization of glyoxal/glyoxylic acid and EPR shows the formation of radical structures.

Zitierung

Mohsin, G. F., Schmitt, F.-J., Kanzler, C., Epping, J. D., Flemig, S., & Hornemann, A. (2018). Structural characterization of melanoidin formed from D-glucose and L-alanine at different temperatures applying FTIR, NMR, EPR, and MALDI-ToF-MS. Food Chemistry, 245(4), 761–767. https://doi.org/10.1016/j.foodchem.2017.11.115

Exportieren

PTB-Publica Menü

Sprache wechseln: uk flag