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. 1994 Dec;106(4):1421–1427. doi: 10.1104/pp.106.4.1421

Regulation of Alternative Oxidase Activity by Pyruvate in Soybean Mitochondria.

D A Day 1, A H Millar 1, J T Wiskich 1, J Whelan 1
PMCID: PMC159681  PMID: 12232419

Abstract

The regulation of alternative oxidase activity by the effector pyruvate was investigated in soybean (Glycine max L.) mitochondria using developmental changes in roots and cotyledons to vary the respiratory capacity of the mitochondria. Rates of cyanide-insensitive oxygen uptake by soybean root mitochondria declined with seedling age. Immunologically detectable protein levels increased slightly with age, and mitochondria from younger, more active roots had less of the protein in the reduced form. Addition of pyruvate stimulated cyanide-insensitive respiration in root mitochondria, up to the same rate, regardless of seedling age. This stimulation was reversed rapidly upon removal of pyruvate, either by pelleting mitochondria (with succinate as substrate) or by adding lactate dehydrogenase with NADH as substrate. In mitochondria from cotyledons of the same seedlings, cyanide-insensitive NADH oxidation was less dependent on added pyruvate, partly due to intramitochondrial generation of pyruvate from endogenous substrates. Cyanide-insensitive oxygen uptake with succinate as substrate was greater than that with NADH, in both root and cotyledon mitochondria, but this difference became much less when an increase in external pH was used to inhibit intramitochondrial pyruvate production via malic enzyme. Malic enzyme activity in root mitochondria declined with seedling age. The results indicate that the activity of the alternative oxidase in soybean mitochondria is very dependent on the presence of pyruvate: differences in the generation of intramitochondrial pyruvate can explain differences in alternative oxidase activity between tissues and substrates, and some of the changes that occur during seedling development.

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Selected References

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  1. Bahr J. T., Bonner W. D., Jr Cyanide-insensitive respiration. II. Control of the alternate pathway. J Biol Chem. 1973 May 25;248(10):3446–3450. [PubMed] [Google Scholar]
  2. Brunswick M., June C. H., Finkelman F. D., Mond J. J. Different patterns of inositol polyphosphate production are seen in B lymphocytes after cross-linking of sIg by anti-Ig antibody or by a multivalent anti-Ig antibody dextran conjugate. J Immunol. 1989 Sep 1;143(5):1414–1421. [PubMed] [Google Scholar]
  3. Conley C. A., Hanson M. R. Tissue-Specific Protein Expression in Plant Mitochondria. Plant Cell. 1994 Jan;6(1):85–91. doi: 10.1105/tpc.6.1.85. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Day D. A., Hanson J. B. Pyruvate and malate transport and oxidation in corn mitochondria. Plant Physiol. 1977 Apr;59(4):630–635. doi: 10.1104/pp.59.4.630. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Delves A. C., Mathews A., Day D. A., Carter A. S., Carroll B. J., Gresshoff P. M. Regulation of the soybean-Rhizobium nodule symbiosis by shoot and root factors. Plant Physiol. 1986 Oct;82(2):588–590. doi: 10.1104/pp.82.2.588. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Dry I. B., Moore A. L., Day D. A., Wiskich J. T. Regulation of alternative pathway activity in plant mitochondria: nonlinear relationship between electron flux and the redox poise of the quinone pool. Arch Biochem Biophys. 1989 Aug 15;273(1):148–157. doi: 10.1016/0003-9861(89)90173-2. [DOI] [PubMed] [Google Scholar]
  7. Hiser C., McIntosh L. Alternative Oxidase of Potato Is an Integral Membrane Protein Synthesized de Novo during Aging of Tuber Slices. Plant Physiol. 1990 May;93(1):312–318. doi: 10.1104/pp.93.1.312. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Millar A. H., Wiskich J. T., Whelan J., Day D. A. Organic acid activation of the alternative oxidase of plant mitochondria. FEBS Lett. 1993 Aug 30;329(3):259–262. doi: 10.1016/0014-5793(93)80233-k. [DOI] [PubMed] [Google Scholar]
  9. Minagawa N., Yoshimoto A. The induction of cyanide-resistant respiration in Hansenula anomala. J Biochem. 1987 May;101(5):1141–1146. doi: 10.1093/oxfordjournals.jbchem.a121978. [DOI] [PubMed] [Google Scholar]
  10. Moore A. L., Siedow J. N. The regulation and nature of the cyanide-resistant alternative oxidase of plant mitochondria. Biochim Biophys Acta. 1991 Aug 23;1059(2):121–140. doi: 10.1016/s0005-2728(05)80197-5. [DOI] [PubMed] [Google Scholar]
  11. Tobin A., Djerdjour B., Journet E., Neuburger M., Douce R. Effect of NAD on Malate Oxidation in Intact Plant Mitochondria. Plant Physiol. 1980 Aug;66(2):225–229. doi: 10.1104/pp.66.2.225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Umbach A. L., Siedow J. N. Covalent and Noncovalent Dimers of the Cyanide-Resistant Alternative Oxidase Protein in Higher Plant Mitochondria and Their Relationship to Enzyme Activity. Plant Physiol. 1993 Nov;103(3):845–854. doi: 10.1104/pp.103.3.845. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Vanlerberghe G. C., McIntosh L. Coordinate regulation of cytochrome and alternative pathway respiration in tobacco. Plant Physiol. 1992 Dec;100(4):1846–1851. doi: 10.1104/pp.100.4.1846. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Vanlerberghe G. C., McIntosh L. Lower growth temperature increases alternative pathway capacity and alternative oxidase protein in tobacco. Plant Physiol. 1992 Sep;100(1):115–119. doi: 10.1104/pp.100.1.115. [DOI] [PMC free article] [PubMed] [Google Scholar]

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