Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1994 Dec;106(4):1633–1638. doi: 10.1104/pp.106.4.1633

Distribution of Pyruvate Dehydrogenase Complex Activities between Chloroplasts and Mitochondria from Leaves of Different Species.

U Lernmark 1, P Gardestrom 1
PMCID: PMC159707  PMID: 12232437

Abstract

Protoplasts from barley (Hordeum vulgare), pea (Pisum sativum), wheat (Triticum aestivum), and spinach (Spinacia oleracea) leaves were fractionated into chloroplast- and mitochondrion-enriched fractions. Pyruvate dehydrogenase complex capacities in mitochondria (mtPDC) and chloroplasts (cpPDC) were measured in appropriate fractions under conditions optimal for each isozyme. The total cellular capacity of PDC was similar in barley and pea but about 50% lower in wheat and spinach. In pea a distribution of 87% mtPDC and 13% cpPDC was found on a cellular basis. In barley, wheat, and spinach the subcellular distribution was the opposite, with about 15% mtPDC and 85% cpPDC. cpPDC activity was constant at about 0.1 nmol cell-1 h-1 in cells from different regions along the developing barley leaf and showed no correlation with developmental patterns of photosynthetic parameters, such as increasing Chl and NADP-glyceraldehyde-3-phosphate dehydrogenase activity. Similarly, the capacity of the mitochondrial isoform did not change during barley leaf development and had a developmental pattern similar to that of citrate synthase and fumarase. Differences in subcellular distribution of PDCs in barley and pea are proposed to be due to differences in regulation, not to changes in isozyme proportions during leaf development or to species-specific differences in phosphorylation state of mtPDC after organelle separation.

Full Text

The Full Text of this article is available as a PDF (707.2 KB).

Selected References

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

  1. Arnon D. I. COPPER ENZYMES IN ISOLATED CHLOROPLASTS. POLYPHENOLOXIDASE IN BETA VULGARIS. Plant Physiol. 1949 Jan;24(1):1–15. doi: 10.1104/pp.24.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Browse J., Roughan P. G., Slack C. R. Light control of fatty acid synthesis and diurnal fluctuations of fatty acid composition in leaves. Biochem J. 1981 Apr 15;196(1):347–354. doi: 10.1042/bj1960347. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Budde R. J., Randall D. D. Pea leaf mitochondrial pyruvate dehydrogenase complex is inactivated in vivo in a light-dependent manner. Proc Natl Acad Sci U S A. 1990 Jan;87(2):673–676. doi: 10.1073/pnas.87.2.673. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Camp P. J., Randall D. D. Purification and Characterization of the Pea Chloroplast Pyruvate Dehydrogenase Complex : A Source of Acetyl-CoA and NADH for Fatty Acid Biosynthesis. Plant Physiol. 1985 Mar;77(3):571–577. doi: 10.1104/pp.77.3.571. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Gardeström P., Edwards G. E. Isolation of Mitochondria from Leaf Tissue of Panicum miliaceum, a NAD-Malic Enzyme Type C(4) Plant. Plant Physiol. 1983 Jan;71(1):24–29. doi: 10.1104/pp.71.1.24. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Gardeström P., Wigge B. Influence of Photorespiration on ATP/ADP Ratios in the Chloroplasts, Mitochondria, and Cytosol, Studied by Rapid Fractionation of Barley (Hordeum vulgare) Protoplasts. Plant Physiol. 1988 Sep;88(1):69–76. doi: 10.1104/pp.88.1.69. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Gemel J., Randall D. D. Light regulation of leaf mitochondrial pyruvate dehydrogenase complex : role of photorespiratory carbon metabolism. Plant Physiol. 1992 Oct;100(2):908–914. doi: 10.1104/pp.100.2.908. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hatch M. D. A simple spectrophotometric assay for fumarate hydratase in crude tissue extracts. Anal Biochem. 1978 Mar;85(1):271–275. doi: 10.1016/0003-2697(78)90299-3. [DOI] [PubMed] [Google Scholar]
  9. Heintze A., Görlach J., Leuschner C., Hoppe P., Hagelstein P., Schulze-Siebert D., Schultz G. Plastidic Isoprenoid Synthesis during Chloroplast Development : Change from Metabolic Autonomy to a Division-of-Labor Stage. Plant Physiol. 1990 Jul;93(3):1121–1127. doi: 10.1104/pp.93.3.1121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Kuhn D. N., Knauf M., Stumpf P. K. Subcellular localization of acetyl-CoA synthetase in leaf protoplasts of Spinacia oleracea. Arch Biochem Biophys. 1981 Jul;209(2):441–450. doi: 10.1016/0003-9861(81)90301-5. [DOI] [PubMed] [Google Scholar]
  11. Murphy D. J., Stumpf P. K. The origin of chloroplastic acetyl coenzyme A. Arch Biochem Biophys. 1981 Dec;212(2):730–739. doi: 10.1016/0003-9861(81)90417-3. [DOI] [PubMed] [Google Scholar]
  12. Randall D. D., Miernyk J. A., Fang T. K., Budde R. J., Schuller K. A. Regulation of the pyruvate dehydrogenase complexes in plants. Ann N Y Acad Sci. 1989;573:192–205. doi: 10.1111/j.1749-6632.1989.tb14997.x. [DOI] [PubMed] [Google Scholar]
  13. Rao K. P., Randall D. D. Plant pyruvate dehydrogenase complex: inactivation and reactivation by phosphorylation and dephosphorylation. Arch Biochem Biophys. 1980 Apr 1;200(2):461–466. doi: 10.1016/0003-9861(80)90377-x. [DOI] [PubMed] [Google Scholar]
  14. Rubin P. M., Randall D. D. Purification and characterization of pyruvate dehydrogenase complex from borccoli floral buds. Arch Biochem Biophys. 1977 Jan 30;178(2):342–349. doi: 10.1016/0003-9861(77)90202-8. [DOI] [PubMed] [Google Scholar]
  15. Sibley M. H., Anderson L. E. Light/Dark modulation of enzyme activity in developing barley leaves. Plant Physiol. 1989 Dec;91(4):1620–1624. doi: 10.1104/pp.91.4.1620. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Smith R. G., Gauthier D. A., Dennis D. T., Turpin D. H. Malate- and pyruvate-dependent Fatty Acid synthesis in leucoplasts from developing castor endosperm. Plant Physiol. 1992 Apr;98(4):1233–1238. doi: 10.1104/pp.98.4.1233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Williams M., Randall D. D. Pyruvate Dehydrogenase Complex from Chloroplasts of Pisum sativum L. Plant Physiol. 1979 Dec;64(6):1099–1103. doi: 10.1104/pp.64.6.1099. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Zeiher C. A., Randall D. D. Identification and Characterization of Mitochondrial Acetyl-Coenzyme A Hydrolase from Pisum sativum L. Seedlings. Plant Physiol. 1990 Sep;94(1):20–27. doi: 10.1104/pp.94.1.20. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES