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首页> 外文期刊>Theoretical and Experimental Plant Physiology >Ascorbic acid toxicity is related to oxidative stress and enhanced by high light and knockdown of chloroplast ascorbate peroxidases in rice plants
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Ascorbic acid toxicity is related to oxidative stress and enhanced by high light and knockdown of chloroplast ascorbate peroxidases in rice plants

机译:抗坏血酸毒性与氧化胁迫有关,并通过水稻植物中的叶绿体抗坏血酸过氧化物酶的高光和敲低而增强

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Toxicity caused by high concentrations of ascorbic acid (AA) has been widely reported in animal cells but is scarcely described in plants. In this study, rice plants deficient (knockdown) in two chloroplast ascorbate peroxidases (APX7/8) and non-transformed (NT) were exposed to wide exogenous AA concentrations in the presence of low light and high light (HL). Reduced (ASC) and oxidized (DHA) ascorbate reached much higher concentrations in symplast compared to the apoplastic space, and high redox states were found in both cellular compartments. Exogenous AA concentrations above 30 mM caused strong cellular and oxidative damage indicated by decreased cell integrity and increased lipid peroxidation in leaves. These toxic effects were strongly enhanced by HL and, to a small extent, by deficiency of both chloroplastic proteins APX7/8. The combination of HL and high AA concentration induced a strong increase in H2O2, associated with decrease in the content of chlorophylls and carotenoids. High AA concentrations strongly induced stomatal closure and impairment in CO2 assimilation, in combination with decreased quantum efficiency of photosystem II (PSII) and PSI. We postulate that oxidative stress caused by AA toxicity in the presence of HL was induced by over-production of reactive oxygen species due to an imbalance between excess energy in the photosystems and low CO2 assimilation, which was related closely to strong decrease in stomatal conductance. In addition, high ASC levels might have acted as a pro-oxidant in the presence of high H2O2 concentrations, stimulating the Fenton reaction and contributing to the intensification of oxidative stress in rice leaves.
机译:由高浓度的抗坏血酸(AA)引起的毒性已被广泛报道动物细胞中,但在植物中几乎没有描述。在该研究中,在两种叶绿体抗坏血酸过氧化物(APX7 / 8)中缺乏(敲低)和未转化的(NT)在低光和高光(HL)存在下暴露于宽外源AA浓度。与痉挛空间相比,减少(ASC)和氧化(DHA)抗坏血酸率达到较高的浓度,并且在两个细胞室中发现了高氧化还原态。外源AA浓度高于30mm,导致细胞完整性降低和叶片中的脂质过氧化增加了强细胞和氧化损伤。通过HL和小程度地,通过叶片蛋白质APX7 / 8的缺乏强烈地增强了这些毒性作用。 HL和高AA浓度的组合诱导H 2 O 2的强烈增加,与叶绿素和类胡萝卜素的含量降低相关。高AA浓度强烈诱导了在CO2同化中的气孔闭合和损伤,相结合了光照II(PSII)和PSI的量子效率。我们假设由于光照中的过量能量和低CO2同化之间的不平衡,通过过度产生,通过过度产生,通过过度产生,通过过度产生的反应性氧气诱导,诱导由HL的毒性引起的氧化应激。此外,在高H2O2浓度存在下,高ASC水平可能是促氧化剂,刺激芬顿反应并有助于稻壳中氧化应激的增强。

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