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Ferritin and iron management in legume plant development and nodulation

机译:豆科植物开发和旋转铁艺和铁路管理

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Iron is one of the most important nutrients for all eukaryotes. However, it is also one of the most dangerous elements. Because of its redox properties, iron is a critical element for such basic processes as DNA and hormone synthesis, respiration and photosynthesis (Briat et al. 1995). Although iron is the fourth most abundant element in the Earth crust, it is not easily available. This is because of low solubility of iron-containing minerals, especially in aerobic and neutral pH environments (Guerinot, Yi 1994). In order to cope with this problem, plants have developed several mechanisms of iron acquisition. Except for morphological changes leading to the extension of active root area, these mechanisms include proton pumping (acidification), secretion of organic acids and phenolics (chelation) and induction of the membrane bound reductase (dicots and nongraminaceous monocots). In addition, high-affinity chelators are used to dissolve Fe(III) oxides (Fox, Guerinot 1998; Hinsinger 1998; Jones 1998; Marschner, Rornheld 1996; Schmidt 1999; Thoiron et al. 1997). However, in the presence of active oxygen species the same desirable iron may catalyze the generation of hydroxyl radicals (OH~.) - the most powerful oxidizing agents known thus far (Fentonreaction) (Cadenas 1989; Meneghini et al. 1995; Nappi, Vass 2000). Attack of toxic oxygen species usually leads to severe results like lipid peroxidation, protein and DNA oxidation and eventually cell disintegration. Plant antioxidant defenses include such compounds like glutathione, ascorbate, carotenoids, tocopherols, etc. Antioxidant enzymes like catalase, peroxidases, dismutases and enzymes of the ascorbate-glutathione cycle are also activated (Becana et al. 1998; Larson 1995). It is obvious that there has to be a strict control of "free" iron in the cell, just to prevent generation of reactive oxygen species (ROS) in the first place. Limited generation of ROS, however, may be a part of plant defense systems against pathogens (Wojtaszek 1997). Predominant portion of cell iron is bound in proteins and enzyme cofactors, but it may easily be "set free" under stress situations.
机译:铁是所有真核生物最重要的营养素之一。但是,它也是最危险的元素之一。由于其氧化还原性能,铁是DNA和激素合成,呼吸和光合作用的这种基本方法的关键因素(Briat等人1995)。虽然铁是地壳中的第四个最丰富的元素,但它不易使用。这是因为含铁矿物质的溶解度低,特别是在有氧和中性pH环境(Guerinot,Yi 1994)中。为了应对这个问题,植物已经开发了几种铁采集机制。除了导致活性根区域的延伸的形态变化,这些机制包括质子泵送(酸化),有机酸分泌和酚类(螯合物)和膜结合还原酶(Dicots和非图形别)的诱导。此外,高亲和力螯合剂用于溶解Fe(III)氧化物(Fox,GueLinot 1998; Hinsinger 1998; Jones 1998; Marschner,Rorrorneld 1996; Schmidt 1999; Thoiron等,1997)。然而,在活性氧物质的存在下,相同的理想铁可以催化羟基自由基的产生(OH〜。) - 迄今为止已知的最强大的氧化剂(髁射)(Cadenas 1989; Meneghini等,1995; Nappi,Vass 2000)。毒性氧气的攻击通常导致严重的结果,如脂质过氧化,蛋白质和DNA氧化,最终细胞崩解。植物抗氧化防御包括如谷胱甘肽,抗坏血酸,类胡萝卜素,生育酚等化合物。还活化了过氧化氢酶,过氧化物酶,乳腺裂解酶的抗氧化酶(BECANA等,1998; Larson 1995)。很明显,必须严格控制细胞中的“免费”铁,只是为了防止在第一处产生反应性氧物种(ROS)。然而,有限的ROS可能是针对病原体的植物防御系统的一部分(Wojtaszek 1997)。细胞铁的主要部分在蛋白质和酶辅助剂中结合,但在应力情况下,它可能很容易“自由”。

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