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首页> 外文期刊>Acta Physiologiae Plantarum >Reactive oxygen species production and antioxidative defense system in pea root tissues treated with lead ions: mitochondrial and peroxisomal level
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Reactive oxygen species production and antioxidative defense system in pea root tissues treated with lead ions: mitochondrial and peroxisomal level

机译:铅离子处理的豌豆根组织中活性氧的产生和抗氧化防御系统:线粒体和过氧化物酶体水平

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Reactive oxygen species (ROS) production and enzymatic antioxidative system [superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APOX), alternative oxidase (AOX)] in nonphotosynthesizing pea plant cells were investigated. From the roots of pea plants cultivated hydroponically on a Hoagland medium with the addition of 0.1 and 0.5 mM of Pb(NO), the three following fractions were isolated by means of a Percoll gradient: cytosol, peroxisomal, and mitochondrial. Lead stress caused HO production in these organelles. The mitochondria from pea cell roots were the main site of HO production. Intensive stress caused by 0.5 mM of Pb(NO) brought about a decrease of HO concentration in mitochondria and peroxisomes after 3 days of the exposition, which was due to an increase of CAT activity. The isoenzymatic profile of antioxidative enzymes indicates mitochondrial and peroxisomal localization of MnSOD and cytoplasmic localization of CuSOD. APOX activity was estimated for all three fractions: cytosol, mitochondria, and peroxisomes. Simultaneously, we observed an increased expression of AOX genes on the basis of the amount of mRNA transcript and confirmed it immunologically on the level of synthesized AOX protein (36 kDa). This has been the first evidence of AOX genes expression of which is induced by the treatment of plants with lead ions and it increases along with the concentration of metal.
机译:研究了非光合作用豌豆植物细胞中活性氧(ROS)的产生和酶促抗氧化系统[超氧化物歧化酶(SOD),过氧化氢酶(CAT),抗坏血酸过氧化物酶(APOX),替代氧化酶(AOX)]。从在Hoagland培养基上水培的豌豆植物的根中,添加0.1和0.5 mM的Pb(NO),通过Percoll梯度分离出以下三个部分:细胞质,过氧化物酶体和线粒体。铅胁迫导致这些细胞器中HO的产生。豌豆细胞根的线粒体是HO产生的主要部位。暴露3天后,由0.5 mM的Pb(NO)引起的强烈压力导致线粒体和过氧化物酶体中HO浓度降低,这是由于CAT活性增加所致。抗氧化酶的同工酶谱表明MnSOD的线粒体和过氧化物酶体定位以及CuSOD的细胞质定位。估计所有三个部分的APOX活性:细胞质,线粒体和过氧化物酶体。同时,我们观察到了基于mRNA转录量的AOX基因表达的增加,并通过免疫学方法在合成的AOX蛋白(36 kDa)的水平上证实了这一点。这是AOX基因表达的第一个证据,其表达是通过用铅离子处理植物诱导的,并且其随金属浓度的增加而增加。

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