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利用6-磷酸葡萄糖和己糖激酶作为ATP再生系统使亚线粒体颗粒中的氧化磷酸化逆转。

Reversal of oxidative phosphorylation in submitochondrial particles using glucose 6-phosphate and hexokinase as an ATP regenerating system.

作者信息

de Meis L, Grieco M A, Galina A

机构信息

Departamento de Bioquímica, Universidade Federal do Rio de Janeiro, Cidade Universitária, Ilha do Fundão, Brazil.

出版信息

FEBS Lett. 1992 Aug 17;308(2):197-201. doi: 10.1016/0014-5793(92)81273-o.

Abstract

During steady-state, the Pi released in the medium is derived from glucose-6-phosphate which continuously regenerates the ATP hydrolyzed. A membrane potential (delta psi) can be built up in submitochondrial particles using glucose-6-phosphate and hexokinase as an ATP-regenerating system. The energy derived from the membrane potential thus formed, can be used to promote the energy-dependent transhydrogenation from NADH to NADP+ and the uphill electron transfer from succinate to NAD+. In spite of the large differences in the energies of hydrolysis of ATP (delta G degrees = -7.0 to -9.0 kcal/mol) and of glucose-6-phosphate (delta G degrees = -2.5 kcal/mol), the same ratio between Pi production and either NADPH or NADH formation were measured regardless of whether millimolar concentrations of ATP or a mixture of ADP, glucose-6-phosphate and hexokinase were used. Rat liver mitochondria were able to accumulate Ca2+ when incubated in a medium containing hexokinase, ADP and glucose-6-phosphate. The different reaction measured with the use of glucose-6-phosphate and hexokinase were inhibited by glucose concentrations varying from 0.2 to 2 mM. Glucose shifts the equilibrium of the reaction towards glucose-6-phosphate formation thus leading to a decrease of the ATP concentration in the medium.

摘要

在稳态期间,培养基中释放的无机磷酸(Pi)来自6-磷酸葡萄糖,后者持续再生被水解的ATP。使用6-磷酸葡萄糖和己糖激酶作为ATP再生系统,可在亚线粒体颗粒中建立膜电位(Δψ)。由此形成的膜电位所产生的能量,可用于促进从NADH到NADP⁺的能量依赖性转氢作用以及从琥珀酸到NAD⁺的上坡电子转移。尽管ATP水解的能量(ΔG° = -7.0至-9.0千卡/摩尔)与6-磷酸葡萄糖水解的能量(ΔG° = -2.5千卡/摩尔)存在很大差异,但无论使用毫摩尔浓度的ATP还是ADP、6-磷酸葡萄糖和己糖激酶的混合物,所测得的Pi产生与NADPH或NADH形成之间的比例相同。当在含有己糖激酶、ADP和6-磷酸葡萄糖的培养基中孵育时,大鼠肝脏线粒体能够积累Ca²⁺。使用6-磷酸葡萄糖和己糖激酶所测得的不同反应受到0.2至2 mM葡萄糖浓度的抑制。葡萄糖使反应平衡向6-磷酸葡萄糖形成方向移动,从而导致培养基中ATP浓度降低。

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