The solutions of 5'-ribonucleotides (inosine or guanosine 5'-monophosphate) or/and D-glucose (Glc) were heated at 90_??_120°C for various reaction times, and the measurements of browning and pH values and analyses of the degradation products from nucleotides or Glc were carried out. Browning reaction of aldoses with phosphate was also examined.
1. It is concluded that phosphate plays an important role in the browning reaction of aldoses with nucleotides, and that the phosphate ester at the primary alcohol of ribose residue, as well as the inorganic orthophosphate which is liberated due to the hydrolysis of the ester is causative of development of the browning.
2. At higher temperature (120°C), the presence of Glc accelerates the degradation of inosine 5'-monophosphate (IMP), and the fact may be attributed to interactions of nucleotides with some reactive compounds such as osones and others which are possibly formed through 1, 2- or/and 2, 3-enolization of aldoses and further degradation, condensation and polymerization.
3. Although IMP is more stable than guanosine 5'-monophosphate (GMP), IMP-Glc solution produced more 3-deoxy-D-glucosone and developed more intense brown color than GMP-Glc solution did, and these differences may be attributed to the amino group on the purine ring in GMP.
4. Though there are some differences in the browning reaction of phosphate- and nucleotide-aldose system, for instance, the dependence of browning on the concentration of IMP or phosphate, browning of both systems are thought to be, as a whole, of similar type considering the similarity in the degradation products of aldose in both browning systems.
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