Nitric oxide degradation by potato tuber mitochondria: Evidence for the involvement of external NAD(P)H dehydrogenases

• Published in: Biochimica et biophysica acta 2008-05, Vol.1777 (5), p.470-476
• Main Authors: de Oliveira, Halley Caixeta, Wulff, Alfredo, Saviani, Elzira Elisabeth, Salgado, Ione
• Format: Article
• Language: English
• Subjects: Calcium - pharmacology; Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone - pharmacology; Electron leakage; External NAD(P)H dehydrogenases; Hydrogen Peroxide - metabolism; Malates - pharmacology; Mitochondria - drug effects; Mitochondria - metabolism; NADH Dehydrogenase - metabolism; NADP - pharmacology; Nitric Oxide - metabolism; Nitric oxide degradation; Plant mitochondria; Potato tuber; Rotenone - pharmacology; Solanum tuberosum - metabolism; Succinic Acid - pharmacology; Superoxide anion; Superoxides - metabolism; Uncoupling Agents - pharmacology
• ISSN: 0005-2728; 0006-3002; 1879-2650
• DOI: 10.1016/j.bbabio.2008.02.006

The mechanisms of nitric oxide (NO) synthesis in plants have been extensively investigated. NO degradation can be just as important as its synthesis in controlling steady-state levels of NO. Here, we examined NO degradation in mitochondria isolated from potato tubers and the contribution of the respiratory chain to this process. NO degradation was faster in mitochondria energized with NAD(P)H than with succinate or malate. Oxygen consumption and the inner membrane potential were transiently inhibited by NO in NAD(P)H-energized mitochondria, in contrast to the persistent inhibition seen with succinate. NO degradation was abolished by anoxia and superoxide dismutase, which suggested that NO was consumed by its reaction with superoxide anion (O 2 −). Antimycin-A stimulated and myxothiazol prevented NO consumption in succinate- and malate-energized mitochondria. Although favored by antimycin-A, NAD(P)H-mediated NO consumption was not abolished by myxothiazol, indicating that an additional site of O 2 − generation, besides complex III, stimulated NO degradation. Larger amounts of O 2 − were generated in NAD(P)H- compared to succinate- or malate-energized mitochondria. NAD(P)H-mediated NO degradation and O 2 − production were stimulated by free Ca 2+ concentration. Together, these results indicate that Ca 2+-dependent external NAD(P)H dehydrogenases, in addition to complex III, contribute to O 2 − production that favors NO degradation in potato tuber mitochondria.