Bashkin P, Sperling O
Biochim Biophys Acta. 1978 Feb 1;538(3):505-11. doi: 10.1016/0304-4165(78)90411-7.
De novo synthesis of purine nucleotides and some regulatory properties of this pathway were studied in cultured epithelial-like rat liver cells. It was found that the physiological 5-phosphoribosyl 1-pyrophosphate (P-Rib-PP) concentration in these cells is limited for purine synthesis de novo. Increase of P-Rib-PP availability, achieved by activation of P-Rib-PP synthetase at high Pi concentration, resulted in acceleration of purine synthesis. The effects of increasing cellular ribose 5-phosphate (Rib-5-P) availability, by methylene blue-induced acceleration of the oxidative pentose phosphate pathway, on P-Rib-PP availability and on the rate of the novo purine synthesis were also studied. It was found that at the Pi concentration prevailing in the tissue at extracellular physiological Pi concentration, Rib-5-P availability is saturating for P-Rib-PP generation and therefore also for purine synthesis.
在培养的大鼠肝上皮样细胞中研究了嘌呤核苷酸的从头合成及其该途径的一些调节特性。发现这些细胞中用于嘌呤从头合成的生理性5-磷酸核糖-1-焦磷酸(P-Rib-PP)浓度有限。通过在高Pi浓度下激活P-Rib-PP合成酶来增加P-Rib-PP的可利用性,导致嘌呤合成加速。还研究了通过亚甲蓝诱导的氧化戊糖磷酸途径加速来增加细胞核糖5-磷酸(Rib-5-P)可利用性对P-Rib-PP可利用性和嘌呤从头合成速率的影响。发现在细胞外生理Pi浓度下组织中占主导的Pi浓度时,Rib-5-P的可利用性对于P-Rib-PP的生成是饱和的,因此对于嘌呤合成也是饱和的。