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Antimycin A treatment decreases respiratory internal rotenone-insensitive NADH oxidation capacity in potato leaves

BACKGROUND: The plant respiratory chain contains several energy-dissipating enzymes, these being type II NAD(P)H dehydrogenases and the alternative oxidase, not present in mammals. The physiological functions of type II NAD(P)H dehydrogenases are largely unclear and little is known about their respo...

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Autores principales: Geisler, Daniela A, Johansson, Fredrik I, Svensson, Å Staffan, Rasmusson, Allan G
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC424582/
https://www.ncbi.nlm.nih.gov/pubmed/15140267
http://dx.doi.org/10.1186/1471-2229-4-8
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author Geisler, Daniela A
Johansson, Fredrik I
Svensson, Å Staffan
Rasmusson, Allan G
author_facet Geisler, Daniela A
Johansson, Fredrik I
Svensson, Å Staffan
Rasmusson, Allan G
author_sort Geisler, Daniela A
collection PubMed
description BACKGROUND: The plant respiratory chain contains several energy-dissipating enzymes, these being type II NAD(P)H dehydrogenases and the alternative oxidase, not present in mammals. The physiological functions of type II NAD(P)H dehydrogenases are largely unclear and little is known about their responses to stress. In this investigation, potato plants (Solanum tuberosum L., cv. Desiree) were sprayed with antimycin A, an inhibitor of the cytochrome pathway. Enzyme capacities of NAD(P)H dehydrogenases (EC 1.6.5.3) and the alternative oxidase were then analysed in isolated leaf mitochondria. RESULTS: We report a specific decrease in internal rotenone-insensitive NADH dehydrogenase capacity in mitochondria from antimycin A-treated leaves. External NADPH dehydrogenase and alternative oxidase capacities remained unaffected by the treatment. Western blotting revealed no change in protein abundance for two characterised NAD(P)H dehydrogenase homologues, NDA1 and NDB1, nor for two subunits of complex I. The alternative oxidase was at most only slightly increased. Transcript levels of nda1, as well as an expressed sequence tag derived from a previously uninvestigated closely related potato homologue, remained unchanged by the treatment. As compared to the daily rhythm-regulated nda1, the novel homologue displayed steady transcript levels over the time investigated. CONCLUSIONS: The internal rotenone-insensitive NADH oxidation decreases after antimycin A treatment of potato leaves. However, the decrease is not due to changes in expression of known nda genes. One consequence of the lower NADH dehydrogenase capacity may be a stabilisation of the respiratory chain reduction level, should the overall capacity of the cytochrome and the alternative pathway be restricted.
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spelling pubmed-4245822004-06-17 Antimycin A treatment decreases respiratory internal rotenone-insensitive NADH oxidation capacity in potato leaves Geisler, Daniela A Johansson, Fredrik I Svensson, Å Staffan Rasmusson, Allan G BMC Plant Biol Research Article BACKGROUND: The plant respiratory chain contains several energy-dissipating enzymes, these being type II NAD(P)H dehydrogenases and the alternative oxidase, not present in mammals. The physiological functions of type II NAD(P)H dehydrogenases are largely unclear and little is known about their responses to stress. In this investigation, potato plants (Solanum tuberosum L., cv. Desiree) were sprayed with antimycin A, an inhibitor of the cytochrome pathway. Enzyme capacities of NAD(P)H dehydrogenases (EC 1.6.5.3) and the alternative oxidase were then analysed in isolated leaf mitochondria. RESULTS: We report a specific decrease in internal rotenone-insensitive NADH dehydrogenase capacity in mitochondria from antimycin A-treated leaves. External NADPH dehydrogenase and alternative oxidase capacities remained unaffected by the treatment. Western blotting revealed no change in protein abundance for two characterised NAD(P)H dehydrogenase homologues, NDA1 and NDB1, nor for two subunits of complex I. The alternative oxidase was at most only slightly increased. Transcript levels of nda1, as well as an expressed sequence tag derived from a previously uninvestigated closely related potato homologue, remained unchanged by the treatment. As compared to the daily rhythm-regulated nda1, the novel homologue displayed steady transcript levels over the time investigated. CONCLUSIONS: The internal rotenone-insensitive NADH oxidation decreases after antimycin A treatment of potato leaves. However, the decrease is not due to changes in expression of known nda genes. One consequence of the lower NADH dehydrogenase capacity may be a stabilisation of the respiratory chain reduction level, should the overall capacity of the cytochrome and the alternative pathway be restricted. BioMed Central 2004-05-12 /pmc/articles/PMC424582/ /pubmed/15140267 http://dx.doi.org/10.1186/1471-2229-4-8 Text en Copyright © 2004 Geisler et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Geisler, Daniela A
Johansson, Fredrik I
Svensson, Å Staffan
Rasmusson, Allan G
Antimycin A treatment decreases respiratory internal rotenone-insensitive NADH oxidation capacity in potato leaves
title Antimycin A treatment decreases respiratory internal rotenone-insensitive NADH oxidation capacity in potato leaves
title_full Antimycin A treatment decreases respiratory internal rotenone-insensitive NADH oxidation capacity in potato leaves
title_fullStr Antimycin A treatment decreases respiratory internal rotenone-insensitive NADH oxidation capacity in potato leaves
title_full_unstemmed Antimycin A treatment decreases respiratory internal rotenone-insensitive NADH oxidation capacity in potato leaves
title_short Antimycin A treatment decreases respiratory internal rotenone-insensitive NADH oxidation capacity in potato leaves
title_sort antimycin a treatment decreases respiratory internal rotenone-insensitive nadh oxidation capacity in potato leaves
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC424582/
https://www.ncbi.nlm.nih.gov/pubmed/15140267
http://dx.doi.org/10.1186/1471-2229-4-8
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