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首页> 外文期刊>Cellular and molecular life sciences: CMLS >The purine nucleoside cycle in cell-free extracts of rat brain: evidence for the occurrence of an inosine and a guanosine cycl with distinct metabolic roles
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The purine nucleoside cycle in cell-free extracts of rat brain: evidence for the occurrence of an inosine and a guanosine cycl with distinct metabolic roles

机译:大鼠脑无细胞提取物中的嘌呤核苷循环:证据表明肌苷和鸟苷环具有不同的代谢作用

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The purine nucleoside cycle is a cyclic pathway composed of three cytosolic enzymes, hypoxanthine-guanine phosphoribosyltransferase, IMP-GMP specific 5'-nucleotidase, and purine-nucleoside phosphorylase. It may be considered a 'futile cycle', whose net reaction is the hydrolysis of 5-phosphoribosyl-l-pyrophosphate to inorganic pyrophosphate and ribose 1-phosphate. The availability of a highly purified preparation of cytosolic 5'-nucleotidase prompted us to reconstitute the purine nucleoside cycle. Its kinetics were strikingly similar to those observed when dialyzed extracts of rat brain were used. Thus, when the cycle is started by addition of inorganic phospate (Pi) and hypoxanthine or inosine (the 'inosine cycle'), steady-state levels of the intermediates are observed and the cycle 'turns over' as far as 5-phosphoribosyl-l-pyrophosphate is being consumed. In the presence of ATP, which acts both as an activator of IMP-GMP-specific 5'-nucleotidase and as substrate of nucleoside mono- and di-phosphokinases, no IDP and ITP are formed. The inosine cycle is further favored by the extremely low xanthine oxidase activity. Evidence is presented that ribose 1-phosphate needed to salvage pyrimidine bases in rat brain may arise, at least in part, from the 5-phosphoribosyl-l-pyrophosphate hydrolysis as catalyzed by the inosine cycle, showing that it may function as a link between purine and pyrimidine salvage. When the cycle is started by addition of Pi and guanine (the 'guanosine cycle'), xanthine and xanthosine are formed, in addition to GMP and guanosine, showing that the guanosine cycle 'turns over' in conjunction with the recycling of ribose 1-phosphate for nucleoside interconversion. In the presence of ATP, GDP and GTP are also formed, and the velocity of the cycle is drastically reduced, suggesting that it might metabolically modulate the salvage synthesis of guanyl nucleotides.
机译:嘌呤核苷循环是由三种胞质酶,次黄嘌呤-鸟嘌呤磷酸核糖基转移酶,IMP-GMP特异性5'-核苷酸酶和嘌呤核苷磷酸化酶组成的循环途径。可以将其视为“无效循环”,其净反应是将5-磷酸核糖基-1-焦磷酸酯水解为无机焦磷酸酯和核糖1-磷酸酯。高纯度的胞质5'-核苷酸酶制剂的可用性促使我们重新构建嘌呤核苷循环。其动力学与使用大鼠脑透析提取物时观察到的动力学极为相似。因此,当通过添加无机磷酸盐(Pi)和次黄嘌呤或肌苷开始循环时(“肌苷循环”),可以观察到中间体的稳态水平,并且该循环“翻转”到5-磷酸核糖基-焦磷酸正被消耗掉。在ATP的存在下,它既充当IMP-GMP特异性5'核苷酸酶的激活剂,又充当核苷单磷酸酶和双磷酸激酶的底物,则不会形成IDP和ITP。极低的黄嘌呤氧化酶活性进一步有利于肌苷循环。有证据表明,在肌苷循环的催化下,挽救大鼠脑中嘧啶碱基所需的核糖1-磷酸可能至少部分是由5-磷酸核糖基-1-焦磷酸水解产生的,表明其可能与肌苷之间的联系有关。嘌呤和嘧啶的抢救。通过添加Pi和鸟嘌呤开始循环(“鸟苷循环”),除GMP和鸟苷外,还形成了黄嘌呤和黄嘌呤,表明鸟苷循环“翻转”并结合了核糖1-磷酸用于核苷相互转化。在存在ATP的情况下,也会形成GDP和GTP,并且循环速度会大大降低,这表明它可能在代谢上调节了胍基核苷酸的拯救合成。

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