Lead heavy metal toxicity induced changes on growth and antioxidative enzymes level in water hyacinths [Eichhornia crassipes (Mart.)]
© Srinivasan et al.; licensee Springer 2014
Received: 17 March 2014
Accepted: 26 June 2014
Published: 24 July 2014
Lead (Pb) heavy metal pollution in water bodies is one of the serious problems across the world. This study was designed to find out the effect of Pb toxicity on physiological and biochemical changes in Eichhornia crassipes (water hyacinth) seedlings.
The plant growth was significantly inhibited (50%) at 1000 mg/L Pb concentration. Accumulation of Pb was higher in root than in shoot tissues. The maximum level of Pb accumulation was noticed in roots (5.45%) followed by petiole (2.72%) and leaf tissues (0.66%). Increasing the Pb concentration gradually decreased the chlorophyll content. Intracellular distribution of Pb was also studied using SEM-EDX, where the Pb deposition was observed in both root and leaf tissues. MDA content increased in both the leaf and root tissues up to the 400 mg/L Pb treatment and slightly decreased at higher concentrations. The activity of antioxidative enzymes, such as APX and POX, positively correlated with Pb treatment, while in the case of SOD and CAT enzymes increased up to 800 mg/L treatment and then slightly decreased at higher concentration in both leaf and root tissues.
These results suggest that water hyacinth plants have efficient mechanism to tolerate Pb toxicity, as evidenced by an increased level of antioxidative enzymes. Results clearly indicate that water hyacinth is a feasible plant for hyperaccumulation of heavy metals from polluted wetlands.
KeywordsHeavy metal stress Aquatic plant Reactive oxygen species Lead hyperaccumulation Phytoremediation
Heavy metal pollution has become one of the important environmental problems worldwide. Metal pollutants are particularly difficult to remediate from the soil, water and air because, unlike organic pollutants that can be degraded to harmless small molecules, toxic elements, such as lead, mercury, cadmium, copper and zinc, are immutable by biochemical reactions. Phytoremediation technology has recently started to gain great importance for the removal of elemental pollutants from soil and water. Hyperaccumulator plants represent a resource for phytoremediation of metal polluted sites, as they can tolerate, uptake and translocate high levels of certain heavy metals that would be toxic to most organisms (Meagher and Heaton ).
Among heavy metals, lead (Pb) is one of the most hazardous pollutants of the environment and Pb pollution in air, water and agricultural soil is an ecological concern due to its impact on human health and environment. The main sources of Pb pollution in the environment are mining and smelting of Pb ore, industrial effluents, fertilizers, pesticides, and municipal sewage sludge (Sharma and Dubey ). It has adverse effects on both plant and animals. In plants, lead affects several metabolic activities in different cell components. Lead toxicity leads to decreases in the percentage of seed germination, as well as growth, dry biomass of roots and shoots, disruption of mineral nutrition (Sharma and Dubey ), reduction in cell division and inhibition of photosynthesis (Ekmekci et al. ).
In addition, Pb is reported to produce reactive oxygen species (ROS) and enhance antioxidant enzyme activity in plants (Mishra et al. ). The ROS produced as a result of oxidative stress causes a variety of harmful effects in plant cells, such as inhibition of photosynthetic activity, inhibition of ATP production, lipid peroxidation, and DNA damage (Ruley ). One of the major consequences is the enhanced production of reactive oxygen species (ROS), which damage cell membranes, nucleic acids and chloroplast pigments (Tewari et al. ). A number of different reactive oxygen species, including the superoxide anion (O2-.), singlet oxygen (1O2), hydroxyl radical (·OH) and the hydrogen peroxide (H2O2) are produced when plants are under heavy metal stress, but these ROS can pose a severe threat when produced in larger amounts. Production of excess ROS in heavy metal stressed plants may be a consequence of the distribution of the balance between their production and the antioxidative enzyme activity, composed of enzymic antioxidants, such as superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX) and peroxidase (POX) (Zhang et al. [2007b]; Jiang et al. ). The superoxide radical (O2.-.), is scavenged in stressed plants by superoxide dismutase, which converts O2-. to hydrogen peroxide (H2O2) (Reddy et al. ). H2O2 is scavenged directly by catalase, converting it to H2O and O2. Peroxidases, such as ascorbate peroxidase and peroxidase, also scavenge H2O2 indirectly by combining it with antioxidant compounds such as ascorbate (Yingli et al. ). The effect of Pb stress has been studied recently in various plant species, including Sesbania drummondii (Venkatachalam et al. ); Triticum aestivum L. (Ekmekci et al. ); Sesuvium portulacastrum and Brassica juncea (Zaier et al. ); Salsola passerine and Chenpodium album L. (Hu et al. ); and, in aquatic plants (Zhang et al. [2007a]; Piotrowska et al. ; Singh et al. ). Plants have divergent mechanisms for modulating heavy metal levels to adapt to a change in the concentration of metals in the polluted environment. Heavy metals are toxic to plants if their accumulation levels exceed the detoxification capacity of the plant tissues (Zhang et al. [2007b]).
Aquatic ecosystems are more sensitive to heavy metal pollutants than terrestrial ones. Large quantities of municipal wastes and industrial effluents are being released to the aquatic environment in major cities where the environment is highly polluted by various hazardous chemicals and metals. Therefore, there is an urgent need for a low cost method to remediate the polluted sites. In order to remove the pollutants using phytoremeidation technology, it is essential to identify a suitable aquatic plant species with high biomass. E. crassipes (Water hyacinth) a free floating plant present in aquatic ecosystems, such as ditches, ponds and lakes, was selected for this study. Water hyacinth can be easily cultivated and could produce high biomass in aquatic ecosystems. Though this species has the capacity to accumulate various heavy metals, there is insufficient information about the plant’s response to Pb exposure under hydroponic systems (Mishra et al. ; Odjegba and Fasidi ; Zhang et al. [2007b]; Mahamadi and Nharingo ; Chunkao et al. ; Singh and Kalamdhad ). In this study, we hypothesize that, due to the multi tolerance mechanism, E. crassipes has the potential to deal with stress at the cellular level and we examined its capability to cope with oxidative stress caused by Pb ions at low, medium and high concentrations in the hydroponic solution. When E. crassipes plants were exposed to different doses of Pb ions and growth rate, biomass, photosynthetic apparatus and antioxidant enzymes, SOD, APX, CAT, and POX were determined. The results obtained in the present study could be useful for understanding the role of E. crassipes antioxidative defense system in efficient Pb tolerance and detoxification strategy adopted by the plants.
Plant material and growth conditions
Water hyacinths seedlings were used for this study. The plants were washed thoroughly with tap water followed by de-ionized water. The plants were grown in plastic cups containing Hoagland nutrient solution (500 mL) (Hoagland and Arnon ) with continuous aeration. The pH of the nutrient solution was 5.8. The seedlings were grown in hydroponics under green house condition for 7 days. In order to select the lead concentrations for treatment, various doses of Pb (NO3)2 (0, 100, 200, 300, 400, 500, 600, 700, 800, 900, 1,000 and 1,500 mg/L) were tried in the preliminary screening of the water hyacinths seedlings. Based on the lead toxicity symptoms and physiological growth of the seedlings, the following doses were finally selected and lead treatment was performed for 10 days. Seedlings were treated with different concentrations of Pb (NO3)2 (100, 200, 400, 600, 800, 1000 mg/L), while seedlings without Pb treatment were used as a control. For each treatment, triplicates were maintained. After ten days of treatment, the seedlings were thoroughly washed with EDTA and root, petiole and leaf samples were used for Pb content analysis. In addition, tolerance index, photosynthetic pigments, MDA content and anti-oxidative enzyme activities of the seedlings were also measured. Scanning Electron Microscopic - EDX observations were also performed to determine the localization and translocation path of Pb in plant tissues.
Determination of seedlings growth tolerance index (GTI)
Estimation of seedling biomass and relative water content (RWC)
Lead content analysis and translocation factor
Estimation of photosynthetic pigment contents
Photosynthetic pigments were extracted from leaves using 80% (v/v) acetone and chlorophyll a, b. Carotenoids content was determined spectrophotometrically at 665, 649 and 470 nm according to (Lichtenthaler ) and expressed in mg/g FW.
Scanning electron microscopy and energy dispersive X-ray spectroscopy
In order to determine the cellular localization of lead, 1000 mg/L of lead treated plant tissues (leaves and roots) were freeze- dried overnight at – 30°C under a vacuum (15–25 torr) using a Labconco’ freeze-dry system (Freezone 4.5, Labconco , Kansas city, MO, USA). Samples were mounted on aluminum stubs with double-sided carbon tape. The SEM observations were performed using a JEOL JSM-5400 LV scanning electron microscope in a low vacuum mode using backscattered electron imaging.
Measurement of MDA contents
Determination of antioxidative enzyme activities
Both root and leaf tissues (>200 mg) from water hyacinth seedlings were homogenized separately in a pre-chilled mortar and pestle under ice-cold conditions with 2.0 ml of extraction buffer [50 mM phosphate buffer (pH 7.5), 0.5 mM ascorbate and 1 mM EDTA]. The homogenate was centrifuged at 10,000 rpm for 15 minutes. The supernatant was used for the measurement of SOD, CAT, APX and POX antioxidative enzyme activities. In addition, the protein content was also measured according to the method of Bradford (), using bovine serum albumin (BSA) as standard.
The SOD activity was quantified by measuring its ability to inhibit the photochemical reduction of nitroblue tetrazolium (NBT) (Beauchamp and Fridovich, ). The reaction mixture (3 ml) contained 100 mM potassium phosphate buffer (pH 7.8), 0.1 mM EDTA, 13 mM methionine, 2.25 mM NBT, 60 μM riboflavin and enzyme extract. After mixing, the contents in the cuvette were illuminated (40 watts light) for 15 minutes. Enzyme extract kept in the dark served as blank, while buffer with no enzyme extract kept in the light served as control. The absorbance was measured at 560 nm against a blank using a UV–visible spectrophotometer. NBT reduction in the light was measured in the presence and absence of enzyme extract. SOD activity was calculated as absorbance of control minus absorbance of sample, giving the total inhibition. One unit of activity was the amount of enzyme required for 50% reduction in color and was expressed in units of the enzyme (mg/protein/h).
Catalase activity was determined by measuring the decomposition of hydrogen peroxide. About 100 μl of enzyme extract was added into the reaction mixture containing 50 mM phosphate buffer (pH 7.0) and 20 mM H2O2. The decrease of the absorbance at 240 nm was recorded. Activity was calculated using an extinction coefficient of 39.04 mM−1 cm−1. One unit of CAT activity was defined as the amount required for decomposing 1 μmol of hydrogen peroxide/min/mg protein under assay conditions (Beer and Sizer ).
APX activity was measured according to the method of Nakano and Asada (). The reaction mixture (3 ml) contained 100 mM potassium phosphate buffer (pH 7.0), 0.5 mM ascorbate, 0.3 mM H2O2 and enzyme extract. The oxidation of ascorbic acid was measured by the decrease in absorbance at 290 nm for 3 min using a UV–visible spectrophotometer. The enzyme activity was calculated using the extinction coefficient 2.8 mM−1 cm−1 and expressed in units/mg protein. One unit of enzyme was the amount necessary to decompose 1 μmol of substrate/min at 25 ºC.
POX activity was estimated according to the method of Zhang et al. (). The reaction mixture (3 ml) contained 100 mM potassium phosphate buffer (pH 6.1), 96 mM guaiacol, 12 mM H2O2 and enzyme extract. The oxidation of guaiacol was measured by the increase in absorbance at 470 nm. The enzyme activity was calculated using the extinction coefficient 25.5 mM−1 cm−1 and expressed in units (mg/protein). One unit of enzyme was the amount necessary to decompose 1 μmol of substrate per min.
Each experiment was performed in triplicate and data was recorded. Statistical analysis was performed using Graphpad InStat Software. Significant differences among treatments were analyzed by one-way ANOVA, using p ≤ 0.05 as a significant level and Tukey-Kramer multiple comparisons tests conducted for pair wise comparisons between treatments.
Effect of Pb concentration on seedlings growth, biomass and relative water content
Effects of lead heavy metal exposure on growth parameters of E. crassipes seedlings
Pb Conc. (mg/L)
Root length (cm)
Shoot length (cm)
Growth rate inhibition (GRI)%
22.33 ± 0.81a*
23.83 ± 2.23a*
20.41 ± 1.67b
20.25 ± 0.83b
20.16 ± 0.76b
19.50 ± 0.56b
18.41 ± 0.91c
17.75 ± 1.38c
15.75 ± 1.26d
17.00 ± 0.76c
13.25 ± 1.25d
16.66 ± 1.08d
09.83 ± 0.79e
13.25 ± 0.99e
Effects of lead heavy metal on plant biomass and relative water content (RWC) of E. crassipes seedlings
Pb Conc. (mg/L)
Relative water content (RWC)%
Fresh weight (FW)
Dry weight (DW)
10.03 ± 0.033a*
0.727 ± 0.004a*
92.73 ± 0.06e*
09.95 ± 0.043a
0.712 ± 0.007a
92.84 ± 0.07d
09.63 ± 0.031b
0.640 ± 0.003b
93.35 ± 0.05b
08.84 ± 0.141c
0.564 ± 0.012b
93.61 ± 0.04a
07.95 ± 0.142d
0.532 ± 0.005c
93.30 ± 0.03b
07.26 ± 0.167d
0.500 ± 0.006c
93.11 ± 0.03c
06.90 ± 0.063e
0.485 ± 0.001d
92.97 ± 0.04d
Lead accumulation in water hyacinth seedlings
Effect of Pb on photosynthetic pigment contents
Scanning electron microscopic observations
Effect of Pb stress on MDA content
Effect of Pb exposure on antioxidative enzyme activity
In the present study, the catalase activity showed increases in leaf and root tissues up to 800 mg/L Pb concentration (60% and 177% increment in leaf and root tissues). Thereafter it was slightly decreased at 1000 mg/L (Figure 5b). However, the catalase activity showed 35% and 166% increases even at 1000 mg/L Pb treatment of leaf and root tissues, compared to the control. In general, the catalase activity was significantly increased at increasing concentrations of Pb treatment.
The APX activity in leaf and root tissues was increased significantly with increasing concentrations of Pb up to 1000 mg/L (Figure 5c). APX activity also showed 537% and 55% increases in leaf and root tissues respectively, compared to the control. The present result clearly shows that APX activity was positively correlated with Pb treatment to maintain the balance between the formation of ROS and their removal in water hyacinth seedlings.
The application of different Pb concentrations had significant effects on peroxidase activity in water hyacinth seedlings. The peroxidase activity was increased with increasing the Pb concentration up to 1000 mg/L in both leaf and root tissues (Figure 5d). Compared to the control, POX activity was increased about 589% and 254% in leaf and root tissues, respectively. Data on peroxidase activity was statistically significant and positively correlated with Pb treatment. It was observed that the water hyacinth plant has the ability to maintain high levels of POX activity at higher concentrations of Pb heavy metal treatment.
In this study, the major response of plants to Pb toxicity is the inhibition of plant growth and induction of oxidative stress in plants. There were strong morphological differences between lead-treated and control plants. The absence of visual damage to the seedlings suggests that water hyacinth plants have efficient mechanisms to tolerate Pb metal induced stress under the present experimental conditions. The most noticeable symptoms of Pb toxicity in water hyacinths were the inhibition of plant growth. In addition, plant biomass is a good indicator for characterizing the growth performance of plants in the presence of heavy metal. In the present study, as the lead treatment was reduced, water hyacinth plant growth rates and overall biomass production decreased. Similar response to lead treatment was previously noticed in various plants (Piechalak et al. , ; Brunet et al. ). Decreased plant growth might be associated with the inhibition of mitotic index noticed with Pb and Cd heavy metal treatment (Vecchia et al. ). Relative water content (RWC) change has been suggested as an indicator of phytotoxicity after heavy metal stress (Zn and Cr) in Indian mustard and Chinese brake fern (Su et al. ). Relative water content in leaves was slightly higher in lead treated plants than in the control at the end of the treatment. It is most likely that lead treatment induced stomatal closure, triggered over the course of the experiment due to the atmospheric carbon fixing activities that were compromised as a consequence (Brunet et al. ).
Plant tolerance to heavy metal stress is estimated based on their root and/or shoot growth inhibition by the metal present in a nutrient solution (Michalal and Wierzbicka ; Wang and Zhou ). Earlier studies on the mechanism of Pb toxicity suggested that Pb binds to nucleic acids and causes aggregation and condensation of chromatin, as well as inhibiting the process of replication, transcription and ultimately affecting cell division and plant growth (Johnson ). In addition, other symptom, such as chlorosis and drying of leaf edge has also been reported in Sesbania drummondii following Pb treatment (Venkatachalam et al. ).
Accumulation of heavy metal content in different plant tissues was greatly varied depending on the Pb concentrations. In this study, accumulation of Pb content in roots of water hyacinth plants was significantly higher, followed by petiole and leaf tissues. Depending on the Pb treatment, the translocation of Pb from root to shoot was 38.27%. Roots were washed with EDTA prior to metal analysis. In order to differentiate between exchangeable and non-exchangeable Pb ions, desorption solutions, viz. EDTA and HETDA, have been used earlier on lead-treated root systems (Huang and Cunningham ; Brunet et al. ). It has been reported that short-term Pb exposure mostly consisted of exchangeable Pb ions, while long-term Pb treatment, as was examined in the present experiment, mostly involved non-exchangeable Pb. An efficient Pb accumulation mechanism in water hyacinth roots could represent a new and interesting phenomenon for establishment of phytoremediation strategies, in which higher levels of the contaminant remain tightly attached to plant tissues. Recent reports also show that Pb accumulation was found to be higher in the roots than in the shoots of Brassica rapa (Cenkci et al. ). The ability of the water hyacinth plant in accumulation and tolerance to Pb ions indicates that this plant species may have an efficient hyperaccumulation mechanism for removal of Pb metal ions from contaminated sites and water bodies.
With the accumulation of Pb ions in water hyacinth plant tissues, we observed effects on the photosynthetic pigments and decreased levels of chlorophyll content in this study. Similarly, reductions in the level of photosynthetic pigments, including Chl- a, b and carotenoids, after exposure to heavy metals, including Pb, has been observed in many plant species (Mishra et al. ; Piotrowska et al., ; Singh et al. ). It has also been reported that alterations in photosynthetic activity and the absorption and distribution of essential nutrients lead to reduced plant growth. The reduction of Chl b was more than overall Chl content. This can be associated with the alteration in pigment composition of photosynthetic approach that possesses lower level of light harvesting chlorophyll proteins (LHCPS) (Loggini et al. ; Gill et al. ). The decreased level of LHCPS is an adaptation defense mechanism of leaves and plants, helping them survive under adverse conditions. Photosynthesis in higher plants is more sensitive to heavy metal treatments, affecting biosynthesis of cholorphyll and accessory pigments (Mobin and Khan ; Ahemad and Khan ; Iqbal et al. ; Gill et al. ). It can be assumed that lead may inhibit chlorophyll biosynthesis by impairing the uptake of essential photosynthetic pigment elements, such as magnesium, potassium, calcium and ion (Piotrowska et al. ). EDAX attachment with scanning electron microscopic analysis is known to provide information on the chemical analysis of the fields that are being investigated or the composition at specific locations. The results of SEM studies indicated that more important effect of Pb toxicity was decreasing the stomata ostiole and increasing the size of guard cells. Therefore Pb enters the leaf through stomata openings and their toxicity may disturb the physiological activity of plants (Sharma and Dubey, ). In this study, EDAX with SEM analysis revealed the presence of lead on plant tissues (leaf and root) of 1000 mg/L Pb treatment.
A decreased rate of photosynthetic pigment accumulation in association with Pb treatment may be the consequence of peroxidation of chloroplast membranes due to increased level of ROS generation. This result is consistent with the enhanced level of H2O2 and peroxide production in water hyacinth plants treated with lead. The localization of Pb ions mainly observed in the root xylem suggests that it is the main pathway of Pb transport from root to shoot. Similar observations were also reported by Sharma et al. ().
The present study strongly suggests that Pb toxicity in situ leads to triggers of some of the key enzymes of the antioxidant defense system in water hyacinth plants. To resist oxidative damage, the antioxidant enzymes and certain metabolites, including MDA content present in plants, play a vital role leading to adaptation and the ultimate survival of plants under stress conditions (Zhang et al. [2007b]). MDA is the product of lipid peroxidation when plants are under stress, and it is often used as an indicator of the extent of oxidative stress (Chen et al. ; Hu et al. ). In the present study, MDA content in water hyacinth seedlings was increased significantly up to 400 mg/L of Pb treatment and then slightly decreased at higher concentrations. This is attributed to the activity of antioxidative enzymes to reduce H2O2 levels and therefore minimize the cell damage to membranes (Zhang et al. [2007b]). The present study suggests that Pb toxicity in situ triggers some of the key enzymes involved in antioxidant defense systems in water hyacinth seedlings.
An increased level of antioxidative enzymes involved in H2O2 detoxification, such as superoxide dismutase, catalase, ascorbate peroxidase, and peroxidase was observed in both leaf and root tissues of Pb treated plants, compared with the control. Superoxide dismutase is considered as a first defense system against ROS, as it acts on superoxide free radicals, which are produced in different compartments of the cell and are precursors of the other ROS (Alscher and Erturk ). In general, the current results show an increased level of SOD activity in water hyacinth plants growing under lead treatment. However, the SOD activity was slightly decreased at higher concentrations of Pb (1000 mg/L), probably because of the harmful effects of over-production of H2O2 or its poisonous ROS derivatives. This may be because initially the SOD activity was increased as a result of the formation of ROS by Pb exposure. Similar results were reported by Zhang et al. ([2007a]); Piotrowska et al. () and Feng-tao et al. (). Enhanced level of SOD activity may be attributed to the production of more active oxygen species (AOS) or over expression of genes encoding SOD. A slight decrease in SOD activity noticed at the higher Pb dose may be due to the inhibition of enzyme activity by excess H2O2 content that is a product in various cellular compartments (Mishra et al. ). In many plant species, heavy metals have been reported to cause oxidative damage due to the production of excess ROS (Verma and Dubey ). To resist oxidative damage, the antioxidant enzymes and certain metabolites present in plants play an important role leading to adaptation and ultimate survival of plants under stress conditions (Verma and Dubey ). The enhancement of H2O2 content may be correlated with the increased level of SOD activity following Pb treatment. Therefore, the presence of excess of H2O2 content should be toxic and must be eliminated by conversion of H2O in subsequent reactions. Protecting the Pb stressed plants from the damaging effects of H2O2 requires the induction of different antioxidative enzymes. The activities of CAT, APX and POX were enhanced in water hyacinth plants following Pb exposure. Results showed that CAT activity was significantly increased up to 800 mg/L Pb treatment and slightly decreased at higher Pb concentrations. Catalase involved in the main defense mechanism against accumulation and toxicity of AOS, such as hydrogen peroxide, may play a key role in decreasing H2O2 content levels in plant cells. CAT enzymes eliminate H2O2 by breaking it down directly to form water and oxygen. It is likely that excess production of ROS by heavy metal stress can inactivate CAT activity at higher concentrations of heavy metals, probably by inactivating the enzyme-bound to heme group (Willekens et al. ). Apparently, the decreased CAT activity at high Pb dose was compensated by the enhanced activity of two other H2O2 degrading antioxidative enzymes i.e., APX and POX. Contrary to our results, a decline in the activity of catalase with an increase heavy metal concentration has also been observed in Lemna gibba (Parlak and Yilmaz ) and in Becopa monnera (Mishra et al. ).
In the present study, enhanced APX activity in water hyacinth is generally correlated with an adaptive mechanism to increase levels of AOS content produced by Pb metal ions. Enzymes of ascorbate are localized mainly in chloroplasts and also in other cellular organelles and cytoplasm, where they play important role in combating oxidative stress. APX activity was increased significantly with increasing the concentration of Pb up to 1000 mg/L in leaf and root tissues. A positive correlation between APX activity and excess ROS may be attributed in effective scavenging of H2O2 content to protect stressed plants against oxidative damage induced under lead stress. Similar to the results observed in the present study, an increase in APX activity in plants following exposure of heavy metals was reported by Piotrowska et al. () and Feng-tao et al. ().
Peroxidase is one of the principle enzymes involved in the elimination of active oxygen species (AOS) under stress. POX catalysis H2O2 is dependent oxidation of substrate. Enhanced POX activity levels have been shown to associate with plant adaptation to severe Pb heavy metal stress and the stimulation of POX activity is likely to be involved in excess of H2O2 content detoxification in water hyacinth plants to grow in the presence of 1000 mg/L Pb ions. Peroxidase has a higher affinity for H2O2 than CAT. Pb stress resulted in increased POX activity up to 1000 mg/L Pb treatment of water hyacinth plants. This also indicated that water hyacinth plants more efficiently avoided damaged from heavy metal lead stress. It is reported that POX could function as effective quenchers of reactive intermediary forms of oxygen and peroxy radicals, stimulated by increased heavy metal doses in plant cells (Radotic et al. ). Peroxidase is widely distributed in the plant kingdom and is one of the principle enzymes involved in the elimination of active oxygen species (AOS). POX consumes H2O2 to generate phenoxy compounds that are polymerized to produce cell wall components, such as lignans (Hu et al. ). The present results are in agreement with other reports showing the positive effects of heavy metal treatment on antioxidative defense systems (Hou et al. ; Jin et al. ; Piotrowska et al. ).
At a higher concentration of Pb treatment (1000 mg/L), an increased level of antioxidative enzymes activities in both leaf and root tissues suggests that enhanced levels of ascorbate peroxidase and peroidase in water hyacinth plants upon exposure to Pb. The stimulation of SOD, CAT, POX and APX in response to Pb treatment indicates their role in ROS detoxification in water hyacinth seedlings. In this study, enhanced ascorbate peroxidase and peroxidase activity strongly support the hypothesis that the H2O2 content mobbing ascorbate peroxidase cycle is likely to be activated in water hyacinth treated with Pb heavy metals, especially at 1000 mg/L exposure. An increased activity of the antioxidative enzymes in water hyacinth plants in response to Pb exposure (100 to 1000 mg/L) is likely to protect plants from heavy metal induced oxidative stress by activating multi defense mechanisms and for better growth in polluted environments.
In conclusion, an efficient adaptation to hydroponics and the valuable Pb accumulation observed for water hyacinth plants, especially at higher doses of heavy metal, shows the great potential of this plant species for the decontamination of pollutants in water-based systems. In this study, water hyacinth plants adapted to higher doses of Pb treatment and the level of antioxidative enzymes was enhanced significantly. Results strongly suggest that water hyacinths are not affected by oxidative stress, in spite of the presence of higher dose of Pb in the hydroponic medium, as would be anticipated for a species that has efficiently survived in a highly polluted environment. Therefore, the data obtained could be used to demonstrate how water hyacinths trigger antioxidant reactions upon exposure to Pb. Increased SOD, CAT, APX and POX activity appear to play key roles in the antioxidant defense response of water hyacinth seedlings when exposed to Pb heavy metal toxicity. These findings clearly show that enhanced antioxidant enzyme mechanisms in water hyacinth seedlings to heavy metal stress could help to overcome metal toxicity from ROS detoxification. Interestingly, water hyacinths, with the aid of its root and petiole, could serve as an important plant species in phytoremediation of Pb heavy metal polluted wetland areas where no other species with high biomass is able to grow.
- Ahemad M, Khan MS: Effect of insecticide-tolerant and plant growth-promoting Mesorhizobium on the performance of chickpea grown in insecticide stressed alluvial soils. J Crop Sci Biotechnol 2009, 12: 213–222.View ArticleGoogle Scholar
- Alscher RG, Erturk NL: Role of superoxide dismutases (SODs) in controlling oxidative stress in plants. Environ Exp Bot 2002, 53: 1331–1341.View ArticleGoogle Scholar
- Beauchamp C, Fridovich I: Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Anal Biochem 1971, 44: 276–287.View ArticlePubMedGoogle Scholar
- Beer RF, Sizer IW: A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J Biol Chem 1952, 195: 133–140.Google Scholar
- Bradford MM: A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein binding. Anal Biochem 1976, 72: 248–254.View ArticlePubMedGoogle Scholar
- Brunet J, Repellin A, Varrault G, Terrync N, Zuily-fodil Y: Lead accumulation in the roots of grass pea ( Lathyrus sativusl ): A novel plant for phytoremediation systems? CR Biologies 2008, 331: 859–864.View ArticleGoogle Scholar
- Cenkci S, Hakkıcigerci I, Yıldız M, Ozay C, Bozdag A, Terzi H: Lead contamination reduces chlorophyll biosynthesis and genomic template stability in Brassica rapa L. Environ Exp Bot 2010, 67: 467–473.View ArticleGoogle Scholar
- Chen J, Shiyab S, Han FX, Monts DL, Waggoner AW, Su ZY: Bioaccumulation and physiological effects of mercury in Pteris vittata and Nephrolepis exaltata . Ecotoxicology 2009, 18: 110–121.View ArticlePubMedGoogle Scholar
- Chunkao K, Nimpee C, Duangmal K: The kings initiatives using water hyacinth to remove heavy metals and plant nutrients from wastewater through Bueng Makkasam in Bangkok, Thailand. Ecol Eng 2012, 39: 40–52.View ArticleGoogle Scholar
- Davenport SB, Gallego SM, Benavides MP, Tomarow ML: Behaviour of antioxidant defense system in the adaptive response to salt stress in Helianthus annus L. J Plant Growth Regul 2003, 40: 81–88.View ArticleGoogle Scholar
- Dubey VRS: Lead toxicity induces lipid peroxidation and alters the activities of antioxidant enzymes in growing rice plants. Plant Sci 2003, 164: 645–655.View ArticleGoogle Scholar
- Ekmekci Y, Tanyolac D, Ayhan B: A crop tolerating oxidative stress induced by excess lead: maize. Acta Physiol Plant 2009, 31: 319–330.View ArticleGoogle Scholar
- Feng-tao LI, Jian-min QI, Gao-yang Z, Li-hui L, Ping-ping F, Fen TA, Jian-tang XU: Effect of cadmium stress on the growth antioxidative enzymes and lipid peroxidation in two kenaf ( Hibiscus cannabinus L.) plant seedlings. J Inte Agri 2013, 12: 610–620.View ArticleGoogle Scholar
- Gill SS, Khan N, Tuteja N: Cadmium at high dose perturbs growth, photosynthesis and nitrogen metabolism while at low dose it up regulates sulfur assimilation and antioxidant machinery in garden cress ( Lepidium sativum L.). Plant Sci 2012, 182: 112–120.View ArticlePubMedGoogle Scholar
- Hoagland DR, Arnon DI: The water-culture method for the growing plants without soil. 347. California Agricultural Experimental Station 1950, 347: 1–32.Google Scholar
- Hou W, Chen X, Song G, Wang Q, Chang CC: Effects of copper and cadmium on heavy metal polluted water body restoration by duckweed ( Lemna minor ). Plant Physiol Biochem 2007, 45: 62–69.View ArticlePubMedGoogle Scholar
- Hu R, Sunc K, Suc X, Pana Y, Zhanga Y, Wanga X: Physiological responses and tolerance mechanisms to Pb in two xerophils: Salsola passerina Bunge and Chenopodium album L. J Hazard Mater 2012, 205–206: 131–138.View ArticlePubMedGoogle Scholar
- Huang JW, Cunningham SD: Lead phytoextraction: species variation in lead uptake and translocation. New Phytol 1996, 134: 75–84.View ArticleGoogle Scholar
- Iqbal N, Masood A, Nazar R, Syeed S, Khan NA: Photosynthesis, growth and antioxidant metabolism in mustard ( Brassica juncea L.) cultivars differing in cadmium tolerance. Agri Sci China 2010, 9: 519–527.View ArticleGoogle Scholar
- Israr M, Sahi SV, Datta R, Sarkar D: Bioaccumulation and physiological effects of mercury in Sesbania drummondii . Chemosphere 2006, 65: 591–598.View ArticlePubMedGoogle Scholar
- Jiang N, Luo X, Zeng J, Yang ZR, Zheng LN, Wang ST: Lead toxicity induced growth and antioxidant responses in Luffa cylindrica seedlings. Inter J Agric Biol 2010, 12: 205–210.Google Scholar
- Jin XF, Yang XE, Islam E, Liu D, Mahmood Q: Effects of cadmium on ultrastructure and antioxidative defense system in hyperaccumulator and non-hyperaccumulator ecotypes of Sedum alfredii Hance. J Hazard Mater 2008, 156(1–3):387–397.View ArticlePubMedGoogle Scholar
- Johnson FM: The genetic effects of environmental lead. Mutat Res 1998, 410: 123–140.View ArticlePubMedGoogle Scholar
- Lichtenthaler HK (1987) Chlorophylls and carotenoids: pigments of photosynthetic biomembranes. In: Packer L, Douce R (eds) Plant Cell Membranes. Academic Press San Diego, pp 350–382 Lichtenthaler HK (1987) Chlorophylls and carotenoids: pigments of photosynthetic biomembranes. In: Packer L, Douce R (eds) Plant Cell Membranes. Academic Press San Diego, pp 350–382Google Scholar
- Loggini B, Scartazza A, Brugnoli E, Navari-Izzo F: Antioxidant defense system, pigment composition and photosynthetic efficiency in two wheat cultivars subjected to drought. Plant Physiol 1999, 119: 1091–1099.View ArticlePubMedPubMed CentralGoogle Scholar
- Mahamadi C, Nharingo T: Comparative adsorption of Pb 2+ , Cd 2+ and Zn 2+ ions onto Eichhornia crassipes in binary and ternary system. Bioresour Technol 2010, 101: 859–864.View ArticlePubMedGoogle Scholar
- Marchiol L, Assolari S, Sacco P, Zerbi G: Phytoextractio of heavy metals by canola ( Brassica napus ) and radish ( Raphanus sativus ) grown on multicontaminated soil. Environ Pollu 2004, 132: 21–27.View ArticleGoogle Scholar
- Meagher RB, Heaton ACP: Strategies for the engineered phytoremediation of toxic element pollution: mercury and arsenic. J Indus Micro Biotech 2005, 32: 502–513.View ArticleGoogle Scholar
- Michalal E, Wierzbicka M: Difference in lead tolerance between Allium cepa plants developing from seeds bulbs. Plant Soil 1998, 199: 251–260.View ArticleGoogle Scholar
- Mishra S, Srivastava S, Tripathi R, Kumar R, Seth C, Gupta D: Lead detoxification by coontail ( Ceratophyllum demersum L.) involves induction of phytochelatins and antioxidant system in response to its accumulation. Chemosphere 2006, 65: 1027–1039.View ArticlePubMedGoogle Scholar
- Mishra KK, Rai UN, Prakash O: Bioconcentration and phytotoxicity of Cd in Eichhornia crassipes . Environ Monit Assess 2007, 130: 237–243.View ArticlePubMedGoogle Scholar
- Mobin M, Khan NA: Photosynthetic activity, pigment composition and antioxidative response of two mustard ( Brassica juncea ) cultivars differing in photosynthetic capacity subjected to cadmium stress. J Plant Physiol 2007, 164: 601–610.View ArticlePubMedGoogle Scholar
- Nakano Y, Asada K: Purification of ascorbate peroxidase in spinach chloroplasts: its inactivation in ascorbate depleted medium and reactivation by monodehydroascorbate radical. Plant Cell Physiol 1987, 28: 131–140.Google Scholar
- Odjegba VJ, Fasidi IO: Phytoremediation of heavy metals by Eichhornia crassipes . Environmentalist 2007, 27: 349–355.View ArticleGoogle Scholar
- Parlak KC, Yilmaz DD: Ecophysiological tolerance of Lemna gibba L. exposed to cadmium. Ecotoxicol Environ Saf 2013, 91: 79–85.View ArticleGoogle Scholar
- Piechalak A, Tomaszewska B, Baralkiewicz D, Malecka A: Accumulation and detoxification of lead ions in legumes. Phytochemistry 2002, 60: 153–162.View ArticlePubMedGoogle Scholar
- Piechalak A, Tomaszewska B, Baralkiewicz D: Enhancing phytoremediative ability of Pisum sativum by EDTA application. Phytochemistry 2003, 64: 1239–1251.View ArticlePubMedGoogle Scholar
- Piotrowska A, Bajguz A, Godlewska B, Czerpak R, Kaminska M: Jasmonic acid as modulator of lead toxicity in aquatic plant Wolffia arrhiza (Lamnaceae). Environ Exp Bot 2009, 66: 507–513.View ArticleGoogle Scholar
- Radotic K, Ducic T, Mutavdzic D: Changes in peroxidase activity and isoenzymes in spruce needles after exposure to different concentrations of cadmium. Environ Exp Bot 2000, 44: 105–113.View ArticlePubMedGoogle Scholar
- Reddy AM, Kumar SG, Jyonthsnakumari G, Thimmanaik S, Sudhakar C: Lead induced changes in antioxidant metabolism of horsegram ( Macrotyloma uniflorum [Lam.] Verdc.) and bengalgram ( Cicer arietinum L.). Chemosphere 2005, 60: 97–104.View ArticlePubMedGoogle Scholar
- Ruley AT: Effects of accumulation of lead and synthetic chelators on the physiology and biochemistry of Sesbania drummondii. Western Kentucky University, USA, M.S thesis; 2004.Google Scholar
- Sharma P, Dubey RS: Lead toxicity in plants. Braz J Plant Physiol 2005, 17: 35–52.View ArticleGoogle Scholar
- Sharma NC, Gardea-Torresdey JL, Parsons J, Sahi SV: Chemical speciation and cellular deposition of lead in Sesbania drummondii . Environ Toxicol Chem 2004, 23: 2068–2073.View ArticlePubMedGoogle Scholar
- Singh J, Kalamdhad AS: Assessment of bioavailability and leachability of heavy metals during rotary drum composting of green waste (Water hyacinth). Ecol Eng 2013, 52: 59–69.View ArticleGoogle Scholar
- Singh R, Tripathi RD, Dwivedi S, Kumar A, Trivedi PK, Chakrabarty D: Lead bioaccumulation potential of an aquatic macropyte Najas indica are related to antioxidant system. Bioresour Technol 2010, 101: 3025–3032.View ArticlePubMedGoogle Scholar
- Su Y, Han FX, Sridhar BBM, Monts DL: Phytotoxicity and phytoaccumulation of trivalent and hexavalent chromium in brake fern. Environ Toxicol Chem 2005, 24: 2019–2026.View ArticlePubMedGoogle Scholar
- Tewari RK, Kumar P, Sharma PN, Bisht SS: Modulation of oxidative stress responsive enzymes by excess cobalt. Plant Sci 2002, 162: 381–388.View ArticleGoogle Scholar
- Vecchia FD, Larocca N, Moro I, Defaveri S, Andreoli C, Rascio N: Morphogenetic, ultrastructural and physiological damages suffered by submerged leaves of Elodea canadensis exposed to cadmium. Plant Sci 2005, 168: 329–338.View ArticleGoogle Scholar
- Venkatachalam P, Srivastava AK, Raghothama KG, Sahi SV: Identification of lead-regulated genes by suppression subtractive hybridization in the heavy metal accumulator Sesbania drummondii . Planta 2007, 225: 1353–1365.View ArticlePubMedGoogle Scholar
- Wang M, Zhou Q: Single and joint toxicity of chlorimuron-ethyl, cadmium and copper acting on wheat Triticum aestivum . Ecotoxicol Environ Safe 2005, 60: 169–175.View ArticleGoogle Scholar
- Wilkins DA: The measurement of tolerance to endemic factors by means of root growth. New Phytol 1978, 80: 623–633.View ArticleGoogle Scholar
- Willekens H, Chamnongpol S, Davey M, Schraudner M, Langebartels C, Van Montagu M, Inzé D, Van Camp W: Catalase is a sink for H 2 O 2 and is indispensable for stress defense in C 3 plants. European Mol Biol Org 1997, 16: 4806–4816.View ArticleGoogle Scholar
- Yingli Y, Yang L, Yuanyuan Y, Zhang Xueling X, Wei J, You J, Wenrui W, Wang L, Ruxia R, Shi A: Comparative antioxidative responses and proline metabolism in two wheat cultivars under short term lead stress. Ecotoxicol Environ Safe 2011, 74: 4–8.Google Scholar
- Zaier H, Ghnaya T, Lakhdar A, Baioui R, Ghabriche R, Mnasri M, Sghair S, Lutts S, Abdelly C: Comparative study of Pb-phytoextraction potential in Sesuvium portulacastrum and Brassica juncea : Tolerance and accumulation. J Hazard Mater 2010, 183: 609–615.View ArticlePubMedGoogle Scholar
- Zhang J, Cui S, Li J, Kirkham MB: Protoplasmic factors, antoxidant responses, and chilling resistance in maize. Plant Physiol Biochem 1995, 33: 567–575.Google Scholar
- Zhang C, Zhou W, Zhu D: Physiological responses induced by copper bioaccumulation in Eichhornia crassipes (Mart.). Hydrobiologica 2007, 579: 211–218.View ArticleGoogle Scholar
- Zhang FQ, Wang YS, Lou ZP, Dong JD: Effect of heavy metal stress on antioxidative enzymes and lipid peroxidation in leaves and roots of two mangrove plant seedlings ( Kandelia candel and Bruguiera gymnorrhiza ). Chemosphere 2007, 67: 44–50.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.