The decomposition of 5′-ribonucleotides (5′-RNT) with thorium ion (Th (IV)) was investigated in buffer solutions ranging pH 1 to 12 at 100°C as basic data for an analytical application of Th (IV) to 5′-RNT describing in “The Japanese Standards of Food Additives 3rd Ed.”
5′-Pyrimidine RNT (I) (5′-uridylic and 5′-cytidylic acids) were shown to undergo only dephosphorylation and to give the corresponding ribonucleoside and phosphoric acid all over the range of pH tested, regardless of the presence of Th (IV). In the absence of Th (IV), I were slightly dephosphorylated in acidic media, but in the presence of Th (IV), I liberated much more phosphoric acid and corresponding nucleosides over a wide range of pH being maximum at pH 3, except at around pH 6.
5′-Purine RNT (II) (5′-inosinic, 5′-guanylic and 5′-adenylic acids) were decomposed by two routes, which were dephosphorylation and
N-glycosyl bond cleavage, to the corresponding ribonucleosides and purine bases, and phosphoric acid, especially in acidic media. In the absence of Th (IV), II were slightly dephosphorylated in the pH 1 to 8 region, and preceded by
N-glycosyl bond rupture at pH 1 and 2. In the presence of Th (IV), however, II were much dephosphorylated in a similar manner as I, and dephosphorylation and glycosyl fission took place simultaneously at pH 1-3. The rate of
N-glycosyl bond cleavage of II in acidic media was found to be considerably influenced with Th (IV), using 5′-inosinic acid and its dephosphorylated product, inosine.
Th (IV) was shown not or scarcely to have any effect on other decompositions such as ring breakage and deamination of 5′-RNT.
From the facts described above, it is suggested that Th (IV) can be applied to an analysis of 5′-RNT.
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