Literature DB >> 2001241

Succinate-driven reverse electron transport in the respiratory chain of plant mitochondria. The effects of rotenone and adenylates in relation to malate and oxaloacetate metabolism.

P Rustin1, C Lance.   

Abstract

The effects of rotenone on the succinate-driven reduction of matrix nicotinamide nucleotides were investigated in Percoll-purified mitochondria from potato (Solanum tuberosum) tubers. Depending on the presence of ADP or ATP, rotenone caused an increase or a decrease in the level of reduction of the matrix nicotinamide nucleotides. The increase in the reduction induced by rotenone in the presence of ADP was linked to the oxidation of the malate resulting from the oxidation of succinate. Depending on the experimental conditions, malic enzyme (at pH 6.6 or in the presence of added CoA) or malate dehydrogenase (at pH 7.9) were involved in this oxidation. At pH 7.9, the oxaloacetate produced progressively inhibited the succinate dehydrogenase. In the presence of ATP the production of oxaloacetate was stopped, and succinate dehydrogenase was protected from inhibition by oxaloacetate. However, previously accumulated oxaloacetate transitorily decreased the level of the reduction of the NAD+ driven by succinate, by causing the reversal of the malate dehydrogenase reaction. Under these conditions (i.e. presence of ATP), rotenone strongly inhibited the reduction of NAD+ by succinate-driven reverse electron flow. No evidence for an active reverse electron transport through a rotenone-insensitive path could be obtained. The inhibitory effect of rotenone was masked if malate had previously accumulated, owing to the malate-oxidizing enzymes which reduced part or all of the matrix NAD+.

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Year:  1991        PMID: 2001241      PMCID: PMC1149945          DOI: 10.1042/bj2740249

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  23 in total

1.  Safranine as a probe of the mitochondrial membrane potential.

Authors:  K E Akerman; M K Wikström
Journal:  FEBS Lett       Date:  1976-10-01       Impact factor: 4.124

2.  Use of submitochondrial particles for prediction of chemical toxicity in man.

Authors:  L M Knobeloch; G A Blondin; J M Harkin
Journal:  Bull Environ Contam Toxicol       Date:  1990-05       Impact factor: 2.151

3.  Isolation of subcellular organelles of metabolism on isopycnic sucrose gradients.

Authors:  N E Tolbert
Journal:  Methods Enzymol       Date:  1974       Impact factor: 1.600

4.  Mechanism of inhibition by uncouples of succinate oxidation in isolated mitochondria.

Authors:  S Papa; N E Lofrumento; G Paradies; E Quagliariello
Journal:  Biochim Biophys Acta       Date:  1969-05

5.  Regulatory function of malate dehydrogenase isoenzymes in the cotyledons of mung bean.

Authors:  T Asahi; M Nishimura
Journal:  J Biochem       Date:  1973-02       Impact factor: 3.387

6.  Measurements of membrane potentials in plant mitochondria with the safranine method.

Authors:  A L Moore; W D Bonner
Journal:  Plant Physiol       Date:  1982-11       Impact factor: 8.340

7.  Malate Oxidation in Plant Mitochondria via Malic Enzyme and the Cyanide-insensitive Electron Transport Pathway.

Authors:  P Rustin; F Moreau; C Lance
Journal:  Plant Physiol       Date:  1980-09       Impact factor: 8.340

8.  The Respiratory Chain of Plant Mitochondria: XI. Electron Transport from Succinate to Endogenous Pyridine Nucleotide in Mung Bean Mitochondria.

Authors:  B T Storey
Journal:  Plant Physiol       Date:  1971-12       Impact factor: 8.340

9.  Effects of guanidine inhibitors on mung bean mitochondria.

Authors:  S B Wilson; W D Bonner
Journal:  Plant Physiol       Date:  1970-07       Impact factor: 8.340

10.  Purification and characterization of the rotenone-insensitive NADH dehydrogenase of mitochondria from Arum maculatum.

Authors:  N D Cook; R Cammack
Journal:  Eur J Biochem       Date:  1984-06-15
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  6 in total

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Review 6.  Succinate Dehydrogenase, Succinate, and Superoxides: A Genetic, Epigenetic, Metabolic, Environmental Explosive Crossroad.

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