The deamination of cytidine and cytosine by acidic buffer solutions. Mutagenic implications.
The deamination of cytidine and cytosine by acidic buffer solutions. Mutagenic implications.
复制标题
酸性缓冲溶液使胞苷和胞嘧啶脱氨基。
DOI:
10.1021/bi00871a026
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发表时间:
1966
期刊:
影响因子:
2.9
通讯作者:
R. Klein
中科院分区:
文献类型:
--
作者:
R. Shapiro;R. Klein
The rate of the reaction with cytidine has been studied and appears to be dependent upon the con-centration of buffer anion and of protonated cytidine. In 0.5 m sodium citrate buffer, a rate maximum oc-itrous acid, a potent chemical mutagen, exerts its effect by the deamination of the amino groups of the adenine, cytosine, and guanine residues of the nucleic acids (Schuster and Schramm, 1958). The fact that three bases are attacked has made it difficult, however, to correlate a mutational event with a particular chemical change. We have been studying alternative chemical methods of deamination of the nucleic acidcomponents in order to develop potential mutagenic agents of greater specificity. It is known that adenine, cytosine, and guanine are deaminated during the hydrolysis of nucleic acids under strongly acidic conditions (Jordan, 1960). We have now found that cytidine and cytosine can be deaminated, in acidic buffer solutions of pH up to 5.0, under conditions which donot deaminate adeno-sine or guanosine. In order to find the optimal conditions for this reaction, and to obtain information about the mechanism, we have studied the dependence of the rate of deamination upon the pH, and the type and concentration of the buffer.