RESUMO
The aim of this study was to determine the influence of different heat treatments on the alternative cyanide-resistant oxidase (AOX) capacity and establish a relation between the heat stress tolerance of spring wheat (Triticum aestivum L.), content of water-soluble carbohydrates in leaves and the alternative respiratory pathway (AP) capacity. We identified a positive relation between these studied parameters. Heat exposure at 39 °C for 24 h increased the heat stress tolerance of seedlings, content of water-soluble carbohydrates and AOX capacity, and the AOX capacity was also high after the subsequent influence of heat shock (50 °C for 3 h). The increased AOX capacity correlated with an increased level of water-soluble carbohydrates in leaves. The content of the AOX protein increased after heat exposure at 39 °C (for 3 h and 24 h) and after the subsequent influence of heat shock (50 °C for 1 and 3 h) at 39 °C for 24 h. We also detected that the content of AOX protein isoforms depends on the duration and intensity of heat treatment. It was concluded that AOX plays an important role in the acclimation of plants to high temperatures.
Assuntos
Oxirredutases/fisiologia , Triticum/enzimologia , Metabolismo dos Carboidratos , Resposta ao Choque Térmico , Mitocôndrias/enzimologia , Mitocôndrias/metabolismo , Oxirredução , Oxirredutases/metabolismo , Folhas de Planta/metabolismo , Plântula/enzimologia , Plântula/metabolismo , Plântula/fisiologia , Triticum/metabolismo , Triticum/fisiologiaRESUMO
Mitochondrial respiratory components participate in the maintenance of chloroplast functional activity. This study investigates the effects 48h de-etiolation of spring wheat seedlings (Triticum aestivum L., var. Irgina) on the expression of genes that encode energy-dissipating respiratory components and antioxidant enzymes under continuous light conditions. The expression of AOX1a following the prolonged darkness exhibited a pattern indicating a prominent dependence on light. The expression of other respiratory genes, including NDA2, NDB2, and UCP1b, increased during de-etiolation and dark-to-light transition; however, changes in the expression of these genes occurred later than those in AOX1a expression. A high expression of NDA1 was detected after 12h of de-etiolation. The suppression of AOX1a, NDA2, NDB2, and UCP1b was observed 24h after de-etiolation when the photosynthetic apparatus and its defence systems against excess light were completely developed. The expression patterns of the respiratory genes and several genes encoding antioxidant enzymes (MnSOD, Cu-ZnSOD, t-APX, GR, and GRX) were quite similar. Our data indicate that the induction of nuclear genes encoding respiratory and antioxidant enzymes allow the plants to control reactive oxygen species (ROS) production and avoid oxidative stress during de-etiolation.
Assuntos
Antioxidantes/metabolismo , Mitocôndrias/metabolismo , Folhas de Planta/metabolismo , Proteínas de Plantas/metabolismo , Triticum/metabolismo , Estiolamento/genética , Estiolamento/fisiologia , Regulação da Expressão Gênica de Plantas/genética , Regulação da Expressão Gênica de Plantas/fisiologia , Proteínas Mitocondriais/genética , Proteínas Mitocondriais/metabolismo , Estresse Oxidativo/genética , Estresse Oxidativo/fisiologia , Oxirredutases/genética , Oxirredutases/metabolismo , Fotossíntese/genética , Fotossíntese/fisiologia , Proteínas de Plantas/genética , Espécies Reativas de Oxigênio/metabolismoRESUMO
This study deals with effects of de-etiolation (48h) of spring wheat (Triticum aestivum L., var. Irgina) seedlings on differential expression of AOX1 genes, levels of AOX protein and the alternative respiratory pathway (AP) capacity. As a result of exposure to continuous irradiation of dark-grown wheat seedlings, the respiratory activity and AP capacity in leaves significantly increased during the first 6h of studies. Expression of AOX1a was up-regulated by light and proved consistent with changes in the AP capacity. Effects on expression of AOX1c were less pronounced. Immunoblot analysis showed three distinct bands of AOX with molecular weights of 34, 36 and 38kDa, with no significant changes in the relative levels during de-etiolation. The lack of a clear correlation between AOX protein amount, AOX1a expression, and AP capacity suggests post-translational control of the enzyme activation. The AOX1a suppression and a decrease in the AP capacity correlated with the sugar pool depletion after 24h of the de-etiolation, which may mean a possible substrate dependence of the AOX activity in the green cells. More efficient malate oxidation by mitochondria as well as the higher AOX capacity during the first 6h of de-etiolation was detected, whereas respiration and AOX capacity with exogenous NADH and glycine increased after 6 and 24h, respectively. We conclude that AOX plays an important role during development of an actively photosynthesizing cell, and can rapidly adapt to changes in metabolism and photosynthesis.