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泽蛙红细胞中磷酸己糖支路的调节与速率

Regulation and rate of the hexose monophosphate shunt in Rana ridibunda erythrocytes.

作者信息

Kaloyianni M, Kalomenopoulou M

机构信息

Department of Zoology, University of Thessaloniki, Greece.

出版信息

Comp Biochem Physiol B. 1990;95(2):287-94. doi: 10.1016/0305-0491(90)90078-8.

Abstract
  1. Resting rates of Rana ridibunda erythrocyte glucose consumption and 14CO2 production from 1-14C-glucose were found to be significantly lower than the respective values in human erythrocytes. 2. In the presence of 1-14C-glucose Methylene Blue stimulated 14CO2 production 7-fold, while in the presence of 6-14C-glucose Methylene Blue stimulated 14CO2 production 1.2-fold. 3. The Km of G-6-PD for G-6-P and NADP were 29 and 12 microM, respectively while the Km of 6-PGD for 6-PG and NADP were 83 and 32 microM, respectively. The Ki of G-6-PD and 6-PGD for NADPH were 80 and 12 microM, respectively. 4. Excess amounts of NADP resulted in a significant decrease of 14CO2 production from 1-14C-glucose in total haemolysates. 5. ATP, ADP and fructose diphosphate inhibited both G-6-PD and 6-PGD, the latter being more sensitive than G-6-PD to their inhibitory effect, 2,3-DPG and reduced and oxidized glutathione showed a marked inhibitory effect on 6-PGD, while the phosphorylated trioses inhibited only G-6-PD. 6. Physiological concentrations of oxidized glutathione decreased the inhibition exercised by NADPH on G-6-PD. 7. The possible role of the two dehydrogenases in the regulation of the HMS is discussed.
摘要
  1. 发现食用葡萄糖的食用蛙红细胞的静息率以及1-14C-葡萄糖生成14CO2的静息率显著低于人类红细胞中的相应值。2. 在1-14C-葡萄糖存在的情况下,亚甲蓝刺激14CO2生成增加了7倍,而在6-14C-葡萄糖存在的情况下,亚甲蓝刺激14CO2生成增加了1.2倍。3. 葡萄糖-6-磷酸脱氢酶(G-6-PD)对葡萄糖-6-磷酸(G-6-P)和烟酰胺腺嘌呤二核苷酸磷酸(NADP)的米氏常数(Km)分别为29和12微摩尔,而6-磷酸葡萄糖脱氢酶(6-PGD)对6-磷酸葡萄糖(6-PG)和NADP的Km分别为83和32微摩尔。G-6-PD和6-PGD对还原型辅酶II(NADPH)的抑制常数(Ki)分别为80和12微摩尔。4. 过量的NADP导致总溶血产物中1-14C-葡萄糖生成14CO2的量显著减少。5. 三磷酸腺苷(ATP)、二磷酸腺苷(ADP)和果糖二磷酸抑制G-6-PD和6-PGD,后者对它们的抑制作用比G-6-PD更敏感,2,3-二磷酸甘油酸(2,3-DPG)以及还原型和氧化型谷胱甘肽对6-PGD有显著抑制作用,而磷酸化丙糖仅抑制G-6-PD。6. 氧化型谷胱甘肽的生理浓度降低了NADPH对G-6-PD的抑制作用。7. 讨论了这两种脱氢酶在磷酸戊糖途径调节中的可能作用。

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