Literature DB >> 6337871

Control of mitochondrial respiration.

J M Tager, R J Wanders, A K Groen, W Kunz, R Bohnensack, U Küster, G Letko, G Böhme, J Duszynski, L Wojtczak.   

Abstract

The control theory of Kacser and Burns [in: Rate Control of Biological Processes (Davies, D.D. ed) pp. 65-104, Cambridge University Press, London, 1973] and Heinrich and Rapoport [Eur. J. Biochem. (1974) 42, 97-105] has been used to quantify the amount of control exerted by different steps on mitochondrial oxidative phosphorylation in rat-liver mitochondria. Inhibitors were used to manipulate the amount of active enzyme. The control strength of the adenine nucleotide translocator was measured by carrying out titrations with carboxyatractyloside. In state 4, the control strength of the translocator was found to be zero. As the rate of respiration was increased by adding hexokinase, the control strength of the translocator increased to a maximum value of approximately 30% at approximately 80% of state 3 respiration. In state 3, control of respiration is distributed between a number of steps, including the adenine nucleotide translocator, the dicarboxylate carrier and cytochrome c oxidase. The measured values for the distribution of control agree very well with those calculated with the aid of a model for mitochondrial oxidative phosphorylation developed by Bohnensack et al. [Biochim. Biophys. Acta (1982) 680, 271-280].

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Year:  1983        PMID: 6337871     DOI: 10.1016/0014-5793(83)80330-5

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  41 in total

1.  Tissue variation in the control of oxidative phosphorylation: implication for mitochondrial diseases.

Authors:  R Rossignol; T Letellier; M Malgat; C Rocher; J P Mazat
Journal:  Biochem J       Date:  2000-04-01       Impact factor: 3.857

2.  NADH is specifically channeled through the mitochondrial porin channel in Saccharomyces cerevisiae.

Authors:  N Avéret; H Aguilaniu; O Bunoust; L Gustafsson; M Rigoulet
Journal:  J Bioenerg Biomembr       Date:  2002-12       Impact factor: 2.945

Review 3.  Kinetic studies of ATP synthase: the case for the positional change mechanism.

Authors:  K F LaNoue; J Duszynski
Journal:  J Bioenerg Biomembr       Date:  1992-10       Impact factor: 2.945

4.  Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells.

Authors:  H R Scholte; H F Busch; I E Luyt-Houwen; M H Vaandrager-Verduin; H Przyrembel; W F Arts
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

5.  Is the cytosolic pi concentration a limiting factor for plant cell respiration?

Authors:  F Rebeille; R Bligny; R Douce
Journal:  Plant Physiol       Date:  1984-02       Impact factor: 8.340

6.  Modulation of F0F1-ATP synthase activity by cyclophilin D regulates matrix adenine nucleotide levels.

Authors:  Christos Chinopoulos; Csaba Konràd; Gergely Kiss; Eugeniy Metelkin; Beata Töröcsik; Steven F Zhang; Anatoly A Starkov
Journal:  FEBS J       Date:  2011-02-23       Impact factor: 5.542

7.  Control by cytochrome c oxidase of the cellular oxidative phosphorylation system depends on the mitochondrial energy state.

Authors:  Claudia Piccoli; Rosella Scrima; Domenico Boffoli; Nazzareno Capitanio
Journal:  Biochem J       Date:  2006-06-15       Impact factor: 3.857

Review 8.  Dehydrogenase activation by Ca2+ in cells and tissues.

Authors:  R G Hansford
Journal:  J Bioenerg Biomembr       Date:  1991-12       Impact factor: 2.945

Review 9.  Control of respiration and ATP synthesis in mammalian mitochondria and cells.

Authors:  G C Brown
Journal:  Biochem J       Date:  1992-05-15       Impact factor: 3.857

10.  Regulation of mitochondrial respiration by inorganic phosphate; comparing permeabilized muscle fibers and isolated mitochondria prepared from type-1 and type-2 rat skeletal muscle.

Authors:  Morten Scheibye-Knudsen; Bjørn Quistorff
Journal:  Eur J Appl Physiol       Date:  2008-11-07       Impact factor: 3.078

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