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PLANT PHYSIOLOGY , Vol 111, Issue 2 613-618, Copyright © 1996 by American Society of Plant Biologists
Specificity of the Organic Acid Activation of Alternative Oxidase in Plant Mitochondria
A. H. Millar, MHN. Hoefnagel, D. A. Day and J. T. Wiskich
Division of Biochemistry and Molecular Biology, and The Cooperative Research Centre for Plant Science, Australian National University, Canberra 0200, Australia (A.H.M., D.A.D.)
The claim that succinate and malate can directly stimulate the activity of
the alternative oxidase in plant mitochondria (A.M. Wagner, C.W.M. van den
Bergen, H. Wincencjusz [1995] Plant Physiol 108: 1035-1042) was
reinvestigated using sweet potato (Ipomoea batatas L.) mitochondria. In
whole mitochondria, succinate (in the presence of malonate) and both L- and
D-malate stimulated respiration via alternative oxidase in a pH- (and
NAD+)-dependent manner. Solubilized malic enzyme catalyzed the oxidation of
both L- and D-malate, although the latter at only a low rate and only at
acid pH. In submitochondrial particle preparations with negligible malic
enzyme activity, neither L- nor D-malate stimulated alternative oxidase
activity. However, even in the presence of high malonate concentrations,
some succinate oxidation was observed via the alternative oxidase, giving
the impression of stimulation of the oxidase. Neither L-malate nor
succinate (in the presence of malonate) changed the dependence of
alternative oxidase activity on ubiquinone reduction state in
submitochondrial particles. In contrast, a large change in this dependence
was observed upon addition of pyruvate. Half-maximal stimulation of
alternative oxidase by pyruvate occurred at less than 5 [mu]M in
submitochondrial particles, one-twentieth of that reported for whole
mitochondria, suggesting that pyruvate acts on the inside of the
mitochondrion. We suggest that malate and succinate do not directly
stimulate alternative oxidase, and that reports to the contrary reflect
intra-mitochondrial generation of pyruvate via malic enzyme.
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