In order to better define the mechanism and the products of guanine oxidation within DNA, we investigated the details of the mechanism of guanine oxidation by a metalloporphyrin, Mn-TMPyP, associated to KHSO5 on oligonucleotides. We found that the three major products of guanine oxidation are formed by independent reaction routes. The oxidized guanidinohydantoin (1) and the proposed spiro compound 3 derivatives are not precursors of imidazolone lesion (Iz). These guanine lesions as well as their degradation products, may account for non-detected guanine oxidation products on oxidatively damaged DNA.
CITATION STYLE
Lapi, A., Pratviel, G., & Meunier, B. (2001). Guanine oxidation in double-stranded DNA by MnTMPyP/KHSO5: At least three independent reaction pathways. Metal-Based Drugs, 8(1), 47–56. https://doi.org/10.1155/MBD.2001.47
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