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. 1971 Feb;47(2):236–245. doi: 10.1104/pp.47.2.236

Cyanide-insensitive Respiration in Plant Mitochondria 1

D S Bendall a,2, W D Bonner Jr a
PMCID: PMC365849  PMID: 16657603

Abstract

Pathways of electron transport have been studied in mitochondria isolated from hypocotyls of etiolated mung bean seedlings and skunk cabbage spadices that show cyanide-resistant respiratory activity. The residual flux through cytochrome c oxidase is shown to be small in comparison with the flux through an unidentified alternative oxidase that is known to have a high affinity for oxygen. This alternative oxidase is not a cytochrome. Skunk cabbage and mung bean mitochondria contain cytochromes a and a3 that have absorption peaks differing slightly from those of animal preparations. A slow oxidation-reduction of cytochrome a3-CN has been demonstrated. Cytochromes b undergo oxidation and reduction in the presence of cyanide but play no essential role in the cyanide-resistant pathway. Antimycin inhibits to an extent similar to that of cyanide; the respiratory chain bifurcates on the substrate side of the antimycin-sensitive site. Evidence is presented for the selective inhibition by thiocyanate, α, α′-dipyridyl, and 8-hydroxyquinoline of the alternative oxidase pathway, which may therefore contain a non-heme iron protein.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BENDALL D. S. Cytochromes and some respiratory enzymes in mitochondria from the spadix of Arum maculatum. Biochem J. 1958 Nov;70(3):381–390. doi: 10.1042/bj0700381. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bonner W. D., Bendall D. S. Reversed electron transport in mitochondria from the spadix of Arum maculatum. Biochem J. 1968 Sep;109(3):47P–47P. doi: 10.1042/bj1090047pa. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Chance B., Hackett D. P. The Electron Transfer System of Skunk Cabbage Mitochondria. Plant Physiol. 1959 Jan;34(1):33–49. doi: 10.1104/pp.34.1.33. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. DIXON M. The determination of enzyme inhibitor constants. Biochem J. 1953 Aug;55(1):170–171. doi: 10.1042/bj0550170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Deverall B. J., Daly J. M. Metabolism of Indoleacetic Acid in Rust Diseases. II. Metabolites of Carboxyl-labeled Indoleacetic Acid in Tissues. Plant Physiol. 1964 Jan;39(1):1–9. doi: 10.1104/pp.39.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Gilmour M. V., Wilson D. F., Lemberg R. The low-temperature spectral properties of mammalian cytochromes oxidase. II. The enzyme isolated from beef-heart mitochondria. Biochim Biophys Acta. 1967;143(3):487–499. doi: 10.1016/0005-2728(67)90054-0. [DOI] [PubMed] [Google Scholar]
  7. Hackett D. P., Haas D. W. Oxidative Phosphorylation and Functional Cytochromes in Skunk Cabbage Mitochondria. Plant Physiol. 1958 Jan;33(1):27–32. doi: 10.1104/pp.33.1.27. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Ikuma H., Bonner W. D. Properties of Higher Plant Mitochondria. III. Effects of Respiratory Inhibitors. Plant Physiol. 1967 Nov;42(11):1535–1544. doi: 10.1104/pp.42.11.1535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Lance C., Bonner W. D. The respiratory chain components of higher plant mitochondria. Plant Physiol. 1968 May;43(5):756–766. doi: 10.1104/pp.43.5.756. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Nicholls P., Kimelberg H. K. Cytochromes a and a3. Catalytic activity and spectral shifts in situ and in solution. Biochim Biophys Acta. 1968 Jul 16;162(1):11–21. doi: 10.1016/0005-2728(68)90209-0. [DOI] [PubMed] [Google Scholar]
  11. POTTER V. R., REIF A. E. Inhibition of an electron transport component by antimycin A. J Biol Chem. 1952 Jan;194(1):287–297. [PubMed] [Google Scholar]
  12. Plesnicar M., Bonner W. D., Jr, Storey B. T. Peroxidase associated with higher plant mitochondria. Plant Physiol. 1967 Mar;42(3):366–370. doi: 10.1104/pp.42.3.366. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Storey B. T., Bahr J. T. The respiratory chain of plant mitochondria. I. Electron transport between succinate and oxygen in skunk cabbage mitochondria. Plant Physiol. 1969 Jan;44(1):115–125. doi: 10.1104/pp.44.1.115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Wilson D. F. Azide inhibition of mitochondrial electron transport. II. Spectral changes induced by azide. Biochim Biophys Acta. 1967 May 9;131(3):431–440. doi: 10.1016/0005-2728(67)90003-5. [DOI] [PubMed] [Google Scholar]
  15. Wiskich J. T., Bonner W. D. Preparation and Properties of Sweet Potato Mitochondria. Plant Physiol. 1963 Sep;38(5):594–604. doi: 10.1104/pp.38.5.594. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. YLER D. D., ESTABROOK R. W., SANADI D. R. ELECTRON AND ENERGY REQUIREMENTS FOR CYTOCHROME B REDUCTION DURING THE OXIDATION OF TETRAMETHYL-P-PHENYLENE DIAMINE. Biochem Biophys Res Commun. 1965 Jan 18;18:264–269. doi: 10.1016/0006-291x(65)90751-5. [DOI] [PubMed] [Google Scholar]
  17. Yocum C. S., Hackett D. P. Participation of Cytochromes in the Respiration of the Aroid Spadix. Plant Physiol. 1957 May;32(3):186–191. doi: 10.1104/pp.32.3.186. [DOI] [PMC free article] [PubMed] [Google Scholar]

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