首页> 美国卫生研究院文献>Biochemical Journal >The fate of 14C in glucose 6-phosphate synthesized from 1-14CRibose 5-phosphate by enzymes of rat liver.
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The fate of 14C in glucose 6-phosphate synthesized from 1-14CRibose 5-phosphate by enzymes of rat liver.

机译:通过大鼠肝脏的酶从1-14C核糖5-磷酸合成6-葡萄糖葡萄糖中14 C的命运。

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摘要

1. Glucose 5-phosphate was synthesized from ribose 5-phosphate by an enzyme extract prepared from an acetone-dried powder of rat liver. Three rates of ribose 5-phosphate utilization were observed during incubation for 17 h. An analysis of intermediates and products formed throughout the incubation revealed that as much as 20% of the substrate carbon could not be accounted for. 2. With [1-14C]ribose 5-phosphate as substrate, the specific radioactivity of [14C]glucose 6-phosphate formed was determined at 1, 2, 5 and 30 min and 3, 8 and 17 h. It increased rapidly to 1.9-fold the initial specific radioactivity of [1-14C]ribose 5-phosphate at 3 h and then decreased to a value approximately equal to that of the substrate at 6 h, and finally at 17 h reached a value 0.8-fold that of the initial substrate [1-14C]ribose 5-phosphate. 3. The specific radioactivity of [14C]ribose 5-phosphate decreased to approx. 50% of its inital value during the first 3 h of the incubation and thereafter remained unchanged. 4. The distribution of 14C in the six carbon atoms of [14C]glucose 6-phosphate formed from [1-14C]ribose 5-phosphate at 1, 2, 5 and 30 min and 3, 8 and 17 h was determined. The early time intervals (1--30 min) were characterized by large amounts of 14C in C-2 and in C-6 and with C-1 and C-3 being unlabelled. In contrast, the later time intervals (3--17 h) were characterized by the appearance of 14C in C-1 and C-3 and decreasing amounts of 14C in C-2 and C-6. 5. It is concluded that neither the currently accepted reaction sequence for the non-oxidative pentose phosphate pathway nor the 'defined' pentose phosphate-cycle mechanism can be reconciled with the labelling patterns observed in glucose 6-phosphate formed during the inital 3 h of the incubation.
机译:1.通过从大鼠肝脏的丙酮干燥粉末制备的酶提取物中,从5-磷酸核糖合成5-磷酸葡萄糖。在孵育17小时的过程中,观察到了5种核糖5-磷酸利用率。对整个孵育过程中形成的中间体和产物的分析表明,多达20%的底物碳无法解释。 2.以[1-14C]核糖5-磷酸为底物,在1、2、5和30分钟以及3、8和17小时测定形成的[14C]葡萄糖6-磷酸的比放射性。它在3 h迅速增加到[1-14C]核糖5-磷酸的初始比放射性的1.9倍,然后在6 h降低到大约等于底物的值,最后在17 h达到0.8的值。底物[1-14C]核糖5-磷酸的三倍。 3. [14 C]核糖5-磷酸的比放射性降低至约3。在孵育的前3小时内,其初始值的50%保持不变。 4.确定在1、2、5和30分钟以及3、8和17小时,由[1-14C]核糖5-磷酸形成的[14C]葡萄糖6-磷酸的六个碳原子中14C的分布。早期时间间隔(1--30分钟)的特征是C-2和C-6中含有大量14C,C-1和C-3未标记。相反,较晚的时间间隔(3--17小时)的特征是C-1和C-3中出现14C,C-2和C-6中14C减少。 5.结论是,目前公认的非氧化性戊糖磷酸途径的反应顺序或“确定的”戊糖磷酸循环机制均不能与在孕妇体内最初3小时形成的6-磷酸葡萄糖中观察到的标记模式相吻合。孵化。

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