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PMID: 10393984 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

The alternative oxidase lowers mitochondrial reactive oxygen production in plant cells.

Maxwell DP, Wang Y, McIntosh L

Abstract

Besides the cytochrome c pathway, plant mitochondria have an alternative respiratory pathway that is comprised of a single homodimeric protein, alternative oxidase (AOX). Transgenic cultured tobacco cells with altered levels of AOX were used to test the hypothesis that the alternative pathway in plant mitochondria functions as a mechanism to decrease the formation of reactive oxygen species (ROS) produced during respiratory electron transport. Using the ROS-sensitive probe 2',7'-dichlorofluorescein diacetate, we found that antisense suppression of AOX resulted in cells with a significantly higher level of ROS compared with wild-type cells, whereas the overexpression of AOX resulted in cells with lower ROS abundance. Laser-scanning confocal microscopy showed that the difference in ROS abundance among wild-type and AOX transgenic cells was caused by changes in mitochondrial-specific ROS formation. Mitochondrial ROS production was exacerbated by the use of antimycin A, which inhibited normal cytochrome electron transport. In addition, cells overexpressing AOX were found to have consistently lower expression of genes encoding ROS-scavenging enzymes, including the superoxide dismutase genes SodA and SodB, as well as glutathione peroxidase. Also, the abundance of mRNAs encoding salicylic acid-binding catalase and a pathogenesis-related protein were significantly higher in cells deficient in AOX. These results are evidence that AOX plays a role in lowering mitochondrial ROS formation in plant cells.

MeSH Terms
Arabidopsis/metabolism Cells, Cultured DNA Primers Electron Transport Glutathione Peroxidase/genetics Mitochondria/metabolism Mitochondrial Proteins Oligonucleotides, Antisense/pharmacology Oxidoreductases/antagonists & inhibitors,genetics,metabolism Oxygen Consumption Plant Proteins Plants, Genetically Modified Plants, Toxic Reactive Oxygen Species/metabolism Recombinant Proteins/metabolism Reverse Transcriptase Polymerase Chain Reaction Tobacco/cytology,enzymology,metabolism
Chemicals
DNA Primers Mitochondrial Proteins Oligonucleotides, Antisense Plant Proteins Reactive Oxygen Species Recombinant Proteins Oxidoreductases alternative oxidase Glutathione Peroxidase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Maxwell D P
Department of Energy Plant Research Laboratory, Michigan State University, East Lansing, MI 48824, USA.
Wang Y
McIntosh L
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38 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1999-07-06
Pages
8271-6
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC22224
Subset
IM
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