Degradation of N-(1-Deoxy- d-xylulos-1-yl)glycine and N-(1-Deoxy- d-xylulos-1-yl)proline using thermal treatment.

Summary The formation and degradation of N-(1-Deoxy- d-xylulos-1-yl)glycine and N-(1-Deoxy- d-xylulos-1-yl)proline, derived from the secondary amine Maillard reaction in xylose-amino acid model solutions, were detailed in this study. The identification and quantitative analysis of N-(1-Deoxy- d-xylulos-1-yl)glycine and N-(1-Deoxy- d-xylulos-1-yl)proline were carried out using high-performance anion-exchange chromatography and high-performance liquid chromatography. The formation of intermediate and advanced products derived from N-(1-Deoxy- d-xylulos-1-yl)glycine and N-(1-Deoxy- d-xylulos-1-yl)proline was also tested using an UV-Vis spectrophotometer to gain a better comparing of the degradation process of the two important Maillard reaction products using thermal treatment. Results showed that the degradation of N-(1-Deoxy- d-xylulos-1-yl)glycine was more significant than N-(1-Deoxy- d-xylulos-1-yl)proline. Moreover, xylose was tested in the degradation products of both N-(1-Deoxy- d-xylulos-1-yl)glycine and N-(1-Deoxy- d-xylulos-1-yl)proline, which indicated that the degradation of N-substituted 1-amino-1-deoxyketoses was a reversible reaction to form reducing sugar. [ABSTRACT FROM AUTHOR]