Effects of ultrasound on pH, intermediate products, browning, glycin and glucose contents, reducing power, and antioxidant activity of a glycin-glucose solution were examined. Results showed that the ultrasonic treatment at the intensity of 17.83 W/cm 2 for 50 min resulted in the increases of the solution's absorbance at 294 and 420 nm and the antioxidant activity from approximately 0% to 2.40%, 1.19%, and 18.62%, respectively. At the same time, 21% reduction in glycin and 92% in glucose were observed. Gas chromatography/mass spectrum analysis showed that the ultrasonic treatment induced a Maillard reaction in the model system producing substances including 2,5-dimethyl-pyrazine, trimethyl-pyrazine, (Z)-9-octadecenamide, 1,2-benzenedicarboxylic acid, and mono (2-ethylhexyl) ester. This study indicated that ultrasound, especially at higher intensities, could potentially be employed as a means to promote the Maillard reaction in the glycin-glucose solution.
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 UVVis 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.
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