Department of Environmental Sciences, COMSATS Institute of Information Technology, Vehari, 61100, Pakistan.
Rev Environ Contam Toxicol. 2014;232:1-44. doi: 10.1007/978-3-319-06746-9_1.
As a result of the industrial revolution, anthropogenic activities have enhanced there distribution of many toxic heavy metals from the earth's crust to different environmental compartments. Environmental pollution by toxic heavy metals is increasing worldwide, and poses a rising threat to both the environment and to human health.Plants are exposed to heavy metals from various sources: mining and refining of ores, fertilizer and pesticide applications, battery chemicals, disposal of solid wastes(including sewage sludge), irrigation with wastewater, vehicular exhaust emissions and adjacent industrial activity.Heavy metals induce various morphological, physiological, and biochemical dysfunctions in plants, either directly or indirectly, and cause various damaging effects. The most frequently documented and earliest consequence of heavy metal toxicity in plants cells is the overproduction of ROS. Unlike redox-active metals such as iron and copper, heavy metals (e.g, Pb, Cd, Ni, AI, Mn and Zn) cannot generate ROS directly by participating in biological redox reactions such as Haber Weiss/Fenton reactions. However, these metals induce ROS generation via different indirect mechanisms, such as stimulating the activity of NADPH oxidases, displacing essential cations from specific binding sites of enzymes and inhibiting enzymatic activities from their affinity for -SH groups on the enzyme.Under normal conditions, ROS play several essential roles in regulating the expression of different genes. Reactive oxygen species control numerous processes like the cell cycle, plant growth, abiotic stress responses, systemic signalling, programmed cell death, pathogen defence and development. Enhanced generation of these species from heavy metal toxicity deteriorates the intrinsic antioxidant defense system of cells, and causes oxidative stress. Cells with oxidative stress display various chemical,biological and physiological toxic symptoms as a result of the interaction between ROS and biomolecules. Heavy-metal-induced ROS cause lipid peroxidation, membrane dismantling and damage to DNA, protein and carbohydrates. Plants have very well-organized defense systems, consisting of enzymatic and non-enzymatic antioxidation processes. The primary defense mechanism for heavy metal detoxification is the reduced absorption of these metals into plants or their sequestration in root cells.Secondary heavy metal tolerance mechanisms include activation of antioxidant enzymes and the binding of heavy metals by phytochelatins, glutathione and amino acids. These defense systems work in combination to manage the cascades of oxidative stress and to defend plant cells from the toxic effects of ROS.In this review, we summarized the biochemiCal processes involved in the over production of ROS as an aftermath to heavy metal exposure. We also described the ROS scavenging process that is associated with the antioxidant defense machinery.Despite considerable progress in understanding the biochemistry of ROS overproduction and scavenging, we still lack in-depth studies on the parameters associated with heavy metal exclusion and tolerance capacity of plants. For example, data about the role of glutathione-glutaredoxin-thioredoxin system in ROS detoxification in plant cells are scarce. Moreover, how ROS mediate glutathionylation (redox signalling)is still not completely understood. Similarly, induction of glutathione and phytochelatins under oxidative stress is very well reported, but it is still unexplained that some studied compounds are not involved in the detoxification mechanisms. Moreover,although the role of metal transporters and gene expression is well established for a few metals and plants, much more research is needed. Eventually, when results for more metals and plants are available, the mechanism of the biochemical and genetic basis of heavy metal detoxification in plants will be better understood. Moreover, by using recently developed genetic and biotechnological tools it may be possible to produce plants that have traits desirable for imparting heavy metal tolerance.
由于工业革命,人类活动增强了许多有毒重金属从地壳到不同环境隔室的分布。有毒重金属的环境污染在全球范围内不断增加,对环境和人类健康都构成了日益严重的威胁。植物从各种来源暴露于重金属:矿石的开采和精炼、肥料和农药的应用、电池化学品、固体废物(包括污水污泥)的处置、废水灌溉、车辆废气排放和相邻的工业活动。重金属直接或间接地在植物细胞中引起各种形态、生理和生化功能障碍,并造成各种损害效应。重金属毒性对植物细胞最早和最常记录的后果是活性氧物质(ROS)的过度产生。与铁和铜等氧化还原活性金属不同,重金属(例如 Pb、Cd、Ni、AI、Mn 和 Zn)不能通过参与 Haber Weiss/Fenton 反应等生物氧化还原反应直接生成 ROS。然而,这些金属通过不同的间接机制诱导 ROS 的产生,例如刺激 NADPH 氧化酶的活性、从酶的特定结合位点置换必需的阳离子以及抑制酶的活性与其对酶上的 -SH 基团的亲和力。
在正常条件下,ROS 在调节不同基因的表达中发挥着几个重要的作用。活性氧物质控制着许多过程,如细胞周期、植物生长、非生物胁迫反应、系统信号、程序性细胞死亡、病原体防御和发育。这些物种的增强产生源自重金属毒性会破坏细胞内固有的抗氧化防御系统,并导致氧化应激。细胞受到氧化应激的影响,由于 ROS 和生物分子之间的相互作用,会显示出各种化学、生物和生理毒性症状。重金属诱导的 ROS 会导致脂质过氧化、膜解体和 DNA、蛋白质和碳水化合物的损伤。植物具有非常有组织的防御系统,由酶和非酶抗氧化过程组成。重金属解毒的主要防御机制是减少这些金属进入植物的吸收或在根细胞中隔离它们。
重金属耐受的次要机制包括抗氧化酶的激活和植物螯合肽、谷胱甘肽和氨基酸与重金属的结合。这些防御系统协同工作,管理氧化应激的级联反应,并保护植物细胞免受 ROS 的毒性影响。
在这篇综述中,我们总结了重金属暴露后 ROS 过度产生所涉及的生化过程。我们还描述了与抗氧化防御机制相关的 ROS 清除过程。
尽管在理解 ROS 过度产生和清除的生物化学方面取得了相当大的进展,但我们仍然缺乏对植物重金属排除和耐受能力相关参数的深入研究。例如,关于谷胱甘肽-谷胱甘肽还原酶-硫氧还蛋白系统在植物细胞中 ROS 解毒中的作用的数据还很缺乏。此外,ROS 如何介导谷胱甘肽化(氧化还原信号)仍不完全清楚。同样,在氧化应激下诱导谷胱甘肽和植物螯合肽的情况已经得到很好的报道,但仍未解释为什么有些研究化合物不参与解毒机制。此外,虽然金属转运体和基因表达的作用已经在几种金属和植物中得到很好的确定,但还需要更多的研究。最终,当更多的金属和植物的结果可用时,将更好地理解植物中重金属解毒的生化和遗传基础的机制。此外,通过使用最近开发的遗传和生物技术工具,有可能生产出具有赋予重金属耐受特性的理想性状的植物。