Schützendübel Andres, Polle Andrea
Forstbotanisches Institut, Abteilung I, Forstbotanik und Baumphysiologie, Georg August Universität Göttingen, Büsgenweg 2, 37077 Göttingen, Germany.
J Exp Bot. 2002 May;53(372):1351-65.
The aim of this review is to assess the mode of action and role of antioxidants as protection from heavy metal stress in roots, mycorrhizal fungi and mycorrhizae. Based on their chemical and physical properties three different molecular mechanisms of heavy metal toxicity can be distinguished: (a) production of reactive oxygen species by autoxidation and Fenton reaction; this reaction is typical for transition metals such as iron or copper, (b) blocking of essential functional groups in biomolecules, this reaction has mainly been reported for non-redox-reactive heavy metals such as cadmium and mercury, (c) displacement of essential metal ions from biomolecules; the latter reaction occurs with different kinds of heavy metals. Transition metals cause oxidative injury in plant tissue, but a literature survey did not provide evidence that this stress could be alleviated by increased levels of antioxidative systems. The reason may be that transition metals initiate hydroxyl radical production, which can not be controlled by antioxidants. Exposure of plants to non-redox reactive metals also resulted in oxidative stress as indicated by lipid peroxidation, H(2)O(2) accumulation, and an oxidative burst. Cadmium and some other metals caused a transient depletion of GSH and an inhibition of antioxidative enzymes, especially of glutathione reductase. Assessment of antioxidative capacities by metabolic modelling suggested that the reported diminution of antioxidants was sufficient to cause H(2)O(2) accumulation. The depletion of GSH is apparently a critical step in cadmium sensitivity since plants with improved capacities for GSH synthesis displayed higher Cd tolerance. Available data suggest that cadmium, when not detoxified rapidly enough, may trigger, via the disturbance of the redox control of the cell, a sequence of reactions leading to growth inhibition, stimulation of secondary metabolism, lignification, and finally cell death. This view is in contrast to the idea that cadmium results in unspecific necrosis. Plants in certain mycorrhizal associations are less sensitive to cadmium stress than non-mycorrhizal plants. Data about antioxidative systems in mycorrhizal fungi in pure culture and in symbiosis are scarce. The present results indicate that mycorrhization stimulated the phenolic defence system in the Paxillus-Pinus mycorrhizal symbiosis. Cadmium-induced changes in mycorrhizal roots were absent or smaller than those in non-mycorrhizal roots. These observations suggest that although changes in rhizospheric conditions were perceived by the root part of the symbiosis, the typical Cd-induced stress responses of phenolics were buffered. It is not known whether mycorrhization protected roots from Cd-induced injury by preventing access of cadmium to sensitive extra- or intracellular sites, or by excreted or intrinsic metal-chelators, or by other defence systems. It is possible that mycorrhizal fungi provide protection via GSH since higher concentrations of this thiol were found in pure cultures of the fungi than in bare roots. The development of stress-tolerant plant-mycorrhizal associations may be a promising new strategy for phytoremediation and soil amelioration measures.
本综述的目的是评估抗氧化剂在保护根系、菌根真菌和菌根免受重金属胁迫方面的作用方式和作用。根据其化学和物理性质,可区分出三种不同的重金属毒性分子机制:(a) 通过自氧化和芬顿反应产生活性氧物种;这种反应在铁或铜等过渡金属中很典型,(b) 阻断生物分子中的必需官能团,这种反应主要见于镉和汞等非氧化还原活性重金属,(c) 从生物分子中置换必需金属离子;后一种反应在不同种类的重金属中都会发生。过渡金属会对植物组织造成氧化损伤,但文献调查并未提供证据表明这种胁迫可以通过提高抗氧化系统水平来缓解。原因可能是过渡金属引发羟基自由基的产生,而抗氧化剂无法控制这种产生。植物暴露于非氧化还原活性金属也会导致氧化应激,如脂质过氧化、H(2)O(2) 积累和氧化爆发所示。镉和其他一些金属会导致谷胱甘肽 (GSH) 的短暂消耗,并抑制抗氧化酶,尤其是谷胱甘肽还原酶。通过代谢模型评估抗氧化能力表明,所报道的抗氧化剂减少足以导致 H(2)O(2) 积累。GSH 的消耗显然是镉敏感性的关键步骤,因为 GSH 合成能力提高的植物对镉的耐受性更高。现有数据表明,当镉的解毒速度不够快时,它可能会通过干扰细胞的氧化还原控制,引发一系列导致生长抑制、刺激次生代谢、木质化,最终导致细胞死亡的反应。这种观点与镉导致非特异性坏死的观点相反。某些菌根共生中的植物比非菌根植物对镉胁迫更不敏感。关于纯培养和共生状态下菌根真菌抗氧化系统的数据很少。目前的结果表明,菌根形成刺激了红绒盖牛肝菌 - 松树菌根共生中的酚类防御系统。镉诱导的菌根根系变化不存在或比非菌根根系中的变化小。这些观察结果表明,尽管共生体的根部察觉到了根际条件的变化,但酚类物质典型的镉诱导应激反应得到了缓冲。尚不清楚菌根形成是通过阻止镉进入敏感的细胞外或细胞内位点,还是通过分泌的或内在的金属螯合剂,或通过其他防御系统来保护根系免受镉诱导的损伤。菌根真菌可能通过 GSH 提供保护,因为在真菌的纯培养物中发现这种硫醇的浓度高于裸根中的浓度。培育耐胁迫的植物 - 菌根共生体可能是植物修复和土壤改良措施的一种有前景的新策略。