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First published online March 12, 2008; 10.1104/pp.107.113613

Plant Physiology 147:101-114 (2008)
© 2008 American Society of Plant Biologists

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Right arrow Reactive Oxygen Species
BIOENERGETICS AND PHOTOSYNTHESIS

Decrease in Manganese Superoxide Dismutase Leads to Reduced Root Growth and Affects Tricarboxylic Acid Cycle Flux and Mitochondrial Redox Homeostasis1,[C],[W]

Megan J. Morgan, Martin Lehmann, Markus Schwarzländer, Charles J. Baxter2, Agata Sienkiewicz-Porzucek, Thomas C.R. Williams, Nicolas Schauer, Alisdair R. Fernie, Mark D. Fricker, R. George Ratcliffe, Lee J. Sweetlove* and Iris Finkemeier

Department of Plant Sciences, University of Oxford, Oxford OX1 3RB, United Kingdom (M.J.M., M.S., C.J.B., T.C.R.W., M.D.F., R.G.R., L.J.S., I.F.); and Max-Planck-Institute of Molecular Plant Physiology, 14476 Potsdam-Golm, Germany (M.L., A.S.-P., N.S., A.R.F.)

Superoxide dismutases (SODs) are key components of the plant antioxidant defense system. While plastidic and cytosolic isoforms have been extensively studied, the importance of mitochondrial SOD at a cellular and whole-plant level has not been established. To address this, transgenic Arabidopsis (Arabidopsis thaliana) plants were generated in which expression of AtMSD1, encoding the mitochondrial manganese (Mn)SOD, was suppressed by antisense. The strongest antisense line showed retarded root growth even under control growth conditions. There was evidence for a specific disturbance of mitochondrial redox homeostasis in seedlings grown in liquid culture: a mitochondrially targeted redox-sensitive green fluorescent protein was significantly more oxidized in the MnSOD-antisense background. In contrast, there was no substantial change in oxidation of cytosolically targeted redox-sensitive green fluorescent protein, nor changes in antioxidant defense components. The consequences of altered mitochondrial redox status of seedlings were subtle with no widespread increase of mitochondrial protein carbonyls or inhibition of mitochondrial respiratory complexes. However, there were specific inhibitions of tricarboxylic acid (TCA) cycle enzymes (aconitase and isocitrate dehydrogenase) and an inhibition of TCA cycle flux in isolated mitochondria. Nevertheless, total respiratory CO2 output of seedlings was not decreased, suggesting that the inhibited TCA cycle enzymes can be bypassed. In older, soil-grown plants, redox perturbation was more pronounced with changes in the amount and/or redox poise of ascorbate and glutathione. Overall, the results demonstrate that reduced MnSOD affects mitochondrial redox balance and plant growth. The data also highlight the flexibility of plant metabolism with TCA cycle inhibition having little effect on overall respiratory rates.


1 This work was supported by the Biotechnology and Biological Sciences Research Council United Kingdom (to M.J.M., C.J.B., T.C.R.W., M.D.F., R.G.R., and L.J.S.), the Gatsby Charitable Foundation (to M.S.), the Alexander von Humboldt Foundation (to I.F.), the Max-Planck-Gesellschaft (to A.S., M.L., and A.R.F.), and by the Bundesministerium für Bildung und Forschung in the framework of Deutsch Israeli Projekt award (to N.S.).

2 Present address: Syngenta, Jealott's Hill International Research Centre, Bracknell, Berkshire RG42 6EY, UK.

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Lee J. Sweetlove (lee.sweetlove{at}plants.ox.ac.uk).

[C] Some figures in this article are displayed in color online but in black and white in the print edition.

[W] The online version of this article contains Web-only data.

www.plantphysiol.org/cgi/doi/10.1104/pp.107.113613

* Corresponding author; e-mail lee.sweetlove{at}plants.ox.ac.uk.

Received November 21, 2007; accepted March 3, 2008; published March 12, 2008.




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