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人体红细胞中肌苷酸降解及磷酸核糖-1-磷酸利用的研究。

Studies on IMP degradation and ribose 1-phosphate utilization in human erythrocytes.

作者信息

Gini S, Simonelli C, Ipata P L

出版信息

Int J Biochem. 1987;19(8):699-703. doi: 10.1016/0020-711x(87)90083-8.

Abstract
  1. Intact human red cells do not attack exogenous IMP. The nucleotide is readily broken down by the soluble erythrocyte fraction to inosine, hypoxanthine and ribose 1-phosphate, with a pH optimum of approx. 6.2. 2. Ribose 1-phosphate can be actively reutilized, in the presence of ATP and hypoxanthine, to give IMP, at pH 7.4. The velocity of the IMP salvage synthesis dramatically increases at more alkaline pH values. 3. The two curves relating the velocities of IMP breakdown and of IMP synthesis as a function of hydrogen ion concentration intersect at pH 7.4. 4. The observations might be relevant in the process of purine transport by red cells.
摘要
  1. 完整的人体红细胞不会攻击外源性肌苷一磷酸(IMP)。该核苷酸很容易被可溶性红细胞组分分解为肌苷、次黄嘌呤和磷酸核糖1 - 磷酸,最适pH约为6.2。2. 在ATP和次黄嘌呤存在的情况下,磷酸核糖1 - 磷酸在pH 7.4时可被积极再利用生成IMP。在更碱性的pH值下,IMP补救合成的速度会显著增加。3. 两条分别表示IMP分解速度和IMP合成速度与氢离子浓度关系的曲线在pH 7.4处相交。4. 这些观察结果可能与红细胞嘌呤转运过程有关。

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