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The effect of cadmium on the growth and antioxidant response for freshwater algae Chlorella vulgaris
SpringerPlus volume 5, Article number: 1290 (2016)
The objective of the present work was to evaluate the effect of exogenously applied cadmium on the physiological response of green algae Chlorella vulgaris. The study investigated the long-term effect (18 days) of cadmium on the levels of algae biomass, assimilation pigment composition, soluble protein, oxidative status (production of hydrogen peroxide and superoxide anion), antioxidant enzymes (such as superoxide dismutase, peroxidase, catalase and glutathione reductase enzyme) in C. vulgaris. The results showed that growth, the amount of chlorophyll a (Chl a), chlorophyll b (Chl b) and carotenoids gradually decreased with increasing cadmium over 18 days exposure. Cadmium at concentration of 7 mg L−1 inhibited algal growth expressed as the number of cells. Our research found that C. vulgaris has a high tolerance to cadmium. Contents of chlorophylls (Chl a and Chl b) and carotenoids (Car) of C. vulgaris was significantly decline with rising concentration of cadmium (p < 0.05). The decrease of 54.04 and 93.37 % in Chl a, 60.65 and 74.32 % in Chl b, 50.00 and 71.88 % in total carotenoids was noticed following the treatment with 3 and 7 mg L−1 cadmium doses compared with control treatment, respectively. Cadmium treatments caused a significant change in the physiological competence (calculated as chlorophyll a/b) which increased with increasing Cd(II) doses up to 1 mg L−1 but decreased at 3 mg L−1. While accumulation of soluble protein was enhanced by presence of cadmium, the treatment with cadmium at 3 and 7 mg L−1 increased the concentration of soluble proteins by 88, 95.8 % in C. vulgaris, respectively. Moreover, low doses of cadmium stimulated enzymatic (superoxide dismutase, catalase and glutathione reductase) in C. vulgaris, The content of peroxidase increased with the increasing cadmium concentration, and had slightly decreased at the concentration of 7 mg L−1, but was still higher than control group, which showed that cadmium stress at high concentration mainly peroxidase works in C. vulgaris. And therefore, suppressed reactive oxygen species (hydrogen peroxide and superoxide) accumulated. The present study also showed that cadmium increased oxidative stress and induced antioxidant defense systems against reactive oxygen species. The observation in here analyzed C. vulgaris after exposure to cadmium indicate that hydrogen peroxide, superoxide and peroxidase in the alga with exposure to Cd(II) seemed to be parameters as biomarkers for metal-induced oxidative stress.
Heavy metals are important environmental pollutants, water environmental deterioration caused by heavy metal emissions are increasing, and produce toxic effects on aquatic plants. The bioaccumulation of metals is a useful indicator since metals are not metabolized (Luoma and Rainbow 2005). Heavy metal can accumulate in aquatic animals and aquatic plants, not only effect the growth and development of aquatic animals and aquatic plants seriously, but also may enter the food chain and endanger human health. Algae are the primary producers of water, heavy metals and other pollutants which into the water through various means are first act on the algae, algae-rich contaminants and affect the entire aquatic ecosystem by pass through the food chain (Liu et al. 2008). Recent studies show that algae can enrich metal ions, we can use algae to repair heavy metal contaminated water. Study the algae physiological response mechanism in heavily stress conditions, to explore the mechanism of resistance to heavy metals, can provide a reference for better used in the treatment of heavy metal wastewater. Under normal metabolic process, the enzymatic and non-enzymatic protection system can make the production and eliminate of ROS maintain homeostasis. When subjected to environmental stress, such as, strong light (Romanowska et al. 2008), ultraviolet radiation (Zhang et al. 2005; Schmidt et al. 2011) and heavy metal stress (Dai 2012), will produce reactive oxygen species (ROS), such as superoxide (O 2 −· ), hydroxide (OH−), hydroxyl radical (·OH), hydrogen peroxide (H2O2). Heavy metal has some toxicity; trace amounts of heavy metals can produce toxic effects. Stress leads to plants produce large amounts of reactive oxygen species. ROS can directly damage proteins, amino acids, nucleic acids and membrane lipids. The antioxidant protection system like the superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), glutathione reductase enzyme (GR), et al can remove the excess ROS induced by stress, protecting cells against injury (Zhou et al. 2001). SOD is the first key enzyme to scavenging reactive oxygen species in plants; in organisms it is in an important position in the active oxygen metabolism, which can disproportionate O2 − to be H2O2, thereby protecting cells oxidative free radical damage. POD is also one of a plant antioxidant enzyme defense system, its active can reflect the intensity of antioxidant capacity and the severity of poisoned of plants, and can catalyze the decomposition the toxic substances in a certain range (Zhang et al. 2002). And POD able to restore H2O2 into H2O. CAT is also a ubiquitous enzyme that can remove H2O2 generated in the metabolism in plant. GR plays an important role in the glutathione cycle metabolism, plants can resistant oxidative metabolism by glutathione metabolic cycle. And under stress, the morphology, growth, photosynthetic pigments, cell biology and physiology of algal were also affected (Bouzon et al. 2011; Schmidt et al. 2011).
Chlorella vulgaris is Chlorophyceae, single-cell green freshwater algae, the diameter is 3–8 microns, is a highly efficient photosynthetic plants, and one of the earliest life on earth, is commonly found in freshwater ecosystems. Survival of the green algae in the aquatic environment contaminated with metals depends on its ability to generate and transit signals that adjust the metabolism. Biomarkers can be used to evaluate the ecological risk assessment (Çelekli et al. 2016). Chlorella vulgaris has strong ability to adapt to the environment. In our previous study of the chlorella, our research found that C. vulgaris has a high tolerance to cadmium. Cadmium is one of the most toxic metals. The major sources of cadmium release into the environment by waste streams are electroplating, smelting, alloy manufacturing, pigments, plastic, battery, mining, and refining processes (Gülay and Yakup 2011). But we found that the study on effect of physiological and antioxidant enzymes on C. vulgaris by cadmium is less.
In view of this, the present study was designed to investigate the extent of Cd-induced oxidative stress in C. vulgaris. The effect of various cadmium concentration on C. vulgaris growth, pigments, hydrogen peroxide (H2O2), superoxide anion (O 2 ·− ), SOD, POD, CAT and GR have been investigated. Provide evidence of physiological mechanisms in the aspects of response cadmium stress by plants. The effect of cadmium on algae growth and antioxidant system and the physiological of C. vulgaris response to cadmium stress were analyzed, it aimed to further explore the mechanism of metal toxicity to algae and the mechanism of resistance to heavy metals.
Clonal culture of C. vulgaris was established by micropipette isolation of a single cell from the water sample which was collected from freshwater, Shaanxi Province, China. Cultures were grown under sterile conditions on glass triangular flask with BG11 medium (Stanier et al. 1971). Cultures were maintained at 20 °C under 12 h light: 12 h dark (L: D) cycle and at an illumination of 75 µmol photons m−2 s−1.
Cells were harvested by centrifugation at exponential phase, collected algae (which density was 3 × 104 cells mL−1) were enriched in triplicate with varying Cd(II) supplements in the final concentrations of 0.0, 0.5, 1, 3, 5, 7 mg L−1. In all cases, 3CdSO4·8H2O was used.
Determination of cell growth
Subsamples for cell counting (2 mL) and metal concentration were taken at approximately the same time every day. Samples for enumeration were fixed in Lugo’s solution (final concentration 2 %) and counted in Sedgewick rafter chamber. Biomass is represented by the number of algae (Lundholm et al. 2004).
Measurement of pigments
The chlorophyll was extracted in the dark for 1 h at 65 °C in 5 mL DMSO. After cooling to room temperature and centrifuged at 15,000g for 15 min. The chlorophyll content was estimated according to the equations proposed by Wellburn (1994) using a spectrophotometer at 666, 653, and 750 nm to correct unspecific absorption (Jozef and Martin 2007). To determine the content of “total” carotenoids, absorbance was read at 480 nm. Chl a, Chl b, chlorophyll a + b and total carotenoids were calculated using equations derived from specific absorption coefficients for pure Chl a and Chl b in DMSO (Wellburn 1994). Chlorophyll a/b was used to assess the physiological competence of algal cells.
Measurement of soluble protein
Soluble protein was measured according to Coomassie Brilliant Blue G-250 method (Bradford 1976). Proteins were extracted with 50 mM potassium phosphate buffer (pH 7.0) and estimated using bovine serum albumin as standard. After centrifugation at 5000g at 4 °C for 10 min, the water-soluble protein content of supernatants was measured. Supernatants (1 mL) were added into 5 mL Coomassie Brilliant Blue G-250 and mixed thoroughly. After 10 min, absorbance of samples (2 mL) was spectrophotometrically measured at 595 nm. Each treatment was replicated three times.
Detection of hydrogen peroxide and superoxide anion
Hydrogen peroxide was extracted by potassium phosphate buffer (pH 6.5).Hydrogen peroxide was quantified by the TiCl4 method (Jozef et al. 2009). Phosphate buffer (50 mM, pH: 6.5) was added into crushed culture. After centrifugation, 0.1 % titanium chloride in 20 % H2SO4 (1.5 mL) was added into supernatant (3 mL) and mixed thoroughly. After centrifugation at 15,000g at 4 °C for 20 min. Absorbance was spectrophotometrically measured at 410 nm. The amount of H2O2 was calculated from standardized curve (0.6–1.8 mM) H2O2 in buffer plus 0.5 mL of titanium chloride solution).
Superoxide anion was extracted by potassium phosphate buffer (pH 7.8) and estimated according to Sun and Hu (2005) by monitoring at 530 nm using NaNO3 as standard. Phosphate buffer (65 mM, pH: 7.8) were added into crushed algae solution and then centrifuged. Reaction mixture contained 2 mL of supernatant, 1.5 mL of phosphate buffer, 0.5 mL of hydroxylamine hydrochloride, after mixing, bathed at 25 °C water for 20 min, took 2 mL reaction solution, added 2 mL of sulfanilic and 2 mL of α-naphthylamine, bathed at 30 °C water for 30 min, and measured at 530 nm. Each treatment was replicated three times.
Determination of enzyme activity
Peroxidase (POD) activity was measured according to guaiacol oxidation method (Gao 2005). Each sample had divided into the measuring tube and the blank tube, added with enzyme solution, 0.1 % guaiacol, distilled water, 0.18 % H2O2 (blank tube was not added), accurately react 10 min under 25 °C, 5 % metaphosphoric acid was added to terminate the reaction, measuring the absorbance under 470 nm.
Superoxide dismutase (SOD) activity was determined by tetrazolium reduction method (Gao 2005). One SOD unit was defined as the amount of enzyme required for inhibit 50 % of NBT photoreduction. Each sample was divided into three tubes, the measuring tube, the light control tube and the dark control tube respectively. Each tube was added with 550 mmol L−1 potassium phosphate buffer (pH 7.8), 130 mmol L−1 methionine solution, 750 μmol L−1 NBT solution, 20 μmol L−1 riboflavin solution, 100 μmol L−1 EDTA-Na2, distilled water, and the enzyme solution was added to the measuring tube, the same amount of distilled water was added to the other tubes. Then the tubes were placed under 1000Lx Fluorescent color reaction 15 min, covered with a black cloth to termination the reactions, make the dark control tube as a blank control and measured the absorbance at 560 nm.
Catalase (CAT) activity was determined using UV absorption method (Gao 2005), to reduce 0.1 within 1 min under A 240 was taken as an enzyme activity unit(U). Each sample had two tubes, added with Tris-HCl buffer (pH 7.0), distilled water, one tub was added with live enzymes, another was dead enzyme, preheat 3 min using a water bath at 25 °C, adding 200 mmol L−1 H2O2 and measuring the absorbance under A240 (distilled water zero) immediately.
Glutathione reductase (GR) activity was determined using the method of Schaedle (1977). To decreases 0.1 at A340 per milligram per minute was taken as an enzyme activity. GR catalyze following reaction: GSSH + NADPH → GSH + NADP+. GR activity was determined by measuring the change of NADPH. 1 mL reaction mixture containing 50 mmol L−1 potassium phosphate buffer (pH 7.8), 20 mmol L−1 EDTA, 1.5 mM NADPH, 5 mM GSSG, 200 μL enzyme solution, and measured the change of OD340 in 1 min under 20 °C immediately (extinction coefficient is 6.2 mmol L−1 cm−1).
All determinations were made in triplicate and data are expressed as means ± the standard deviation (SD). Statistical tests were carried out using the software SPASS ver. Differences between individual means were determined by Tukey’s post hoc multiple range test p < 0.05 for this procedure.
Dose-effect of cadmium in C. vulgaris growth and composition of pigments
Growth measured as cell density (Fig. 1). There were significant differences in the cell density of C. vulgaris under high Cd(II) treatments and cell density decreased in response to increasing cadmium doses, as shown in Fig. 1. The inhibited growth was mainly occurred under high cadmium concentration (3 mg L−1, 5 mg L−1), C. vulgaris could not be survived in 7 mg L−1 cadmium concentration. But under low cadmium supplements, there was barely no inhibited even slightly promotion after 12 days, and the effect was not obvious. The result indicted that C. vulgaris can be well tolerated with 1–5 mg L−1 cadmium, although the growth is inhibited under high concentration, C. vulgaris still can be lived in 5 mg L−1. Our research found that C. vulgaris has a high tolerance to cadmium.
Effects of cadmium stress on Chl a, Chl b and total carotenoids of C. vulgaris are presented in Fig. 2. Cadmium had an adverse influence on Chl a production by C. vulgaris. The Chl a content significantly decreased (p < 0.05) from 4.83 to 0.32 µg mg−1, while the Cd(II) concentration was increased from 0 (control) to 7 mg L−1. A similar tendency was observed for Chl b upon cadmium exposure (Fig. 2). The total carotene production by C. vulgaris varied from 0.64 to 0.18 µg mg−1 for the control and 7 mg L−1 Cd(II), respectively. Cd(II) had an adverse effect (p < 0.05) on the total carotene production. The decrease of 54.04 and 93.37 % in Chl a, 60.65 and 74.32 % in Chl b, 50.00 and 71.88 % in total carotenoids was noticed following the treatment with 3 and 7 mg L−1 cadmium doses compared with control treatment, respectively. Cadmium treatments caused a significant change in the physiological competence (calculated as chlorophyll a/b) which increased with increasing Cd(II) doses up to 1 mg L−1 but decreased at 3 mg L−1. Chl a to Chl b ratios revealed that the damaging effect was found to be greater (by 42.6 %) on Chl b at 1 mg L−1 Cd(II) concentration while Chl a was affected more (by 93.4 %) under 7 mg L−1 Cd(II) concentration.
The effect of cadmium on soluble protein content, hydrogen peroxide and superoxide anion content of C. vulgaris
The influence of Cd(II) stress on protein, hydrogen peroxide and superoxide anion contents of C. vulgaris is given in Fig. 3. After 18 days exposure, effect of different Cd(II) concentrations on soluble protein content was significantly altered. Cd(II) stress had a significantly increasing trend on the protein content of C. vulgaris under the concentration 0–7 mg L−1 (Fig. 3).The effect of Cd(II) on hydrogen peroxide and superoxide anion were both significant (p < 0.001) (Fig. 3). Levels of hydrogen peroxide and superoxide anion elevated with increasing Cd content in the medium, significantly under the high concentration of 5 and 7 mg L−1, the hydrogen peroxide contents were increased by 5.90 times and 7.45 times, and superoxide anion were increased by 9.70 times and 14.59 times at 5 and 7 mg L−1 Cd(II) concentration, respectively. The highest contents of these ROS were observed in C. vulgaris cells treated with 7 mg L−1 Cd(II) concentration (7.45 times increase in hydrogen peroxide content, and 14.59 times increase in superoxide anion content) in the 18 days of cultivation.
Activity of antioxidative enzymes
Antioxidant biomarkers, Cd had significant effects on the activities of antioxidant enzymes at most of the experimental doses in comparison with the controls. Cadmium influenced the activity of antioxidant enzymes (SOD, POD, CAT and GR) involved in the scavenging of ROS (Figs. 4, 5, 6). Effect of different concentrations of cadmium on four enzymes was significant. The contents of SOD, CAT, GR were all first increases and then decrease with the cadmium concentration increasing, SOD and CAT content reached a maximum at 0.5 mg L−1 (Fig. 4), GR content reached a maximum at 1 mg L−1 (Fig. 6). The highest enhancement of the activity of antioxidant enzymes (34.18 % SOD, 38.79 % CAT) appeared as a consequence of algal exposure to 0.5 mg L−1 cadmium after 18 days of cultivation. Cadmium applied 1 mg L−1 stimulated the activity of GR by 92.38 %. The content of POD increased with the increasing cadmium concentration, and had slightly decreased at the concentration of 7 mg L−1, but was still higher than control group. The increase in POD level by 1.45 times, 1.26 times, 2.50 times, 3.06 times and 2.40 times was obtained in the culture growing in the presence of 0.5, 1, 3, 5, and 7 mg L−1 cadmium, respectively after 18 days of cultivation (Fig. 5). Results indicated that, 0.5 mg L−1 cadmium stimulated SOD by 34.18 %, CAT by 38.79 %, 1 mg L−1 cadmium enhanced the activity of GR by 92.38 %, whereas cadmium increased the activity of POD after 18 days of cultivation. And showed that cadmium stress at high concentration mainly POD works in C. vulgaris.
Decrease of the growth can be relatively easily determined and reflects physiological status of the algal cells (Juraj et al. 2011). Heavy metals had adverse effects on the growth of Scenedesmus quadricauda (Mohammed and Markert 2006; Stork et al. 2013) and Spirogyra setiformis (Çelekli et al. 2016) in cultures, same result also was found in this study, the inhibited of growth is mainly under high cadmium concentration, the growth of C. vulgaris decreased with the increasing cadmium concentration.
Pigment reduction was reported for S. quadricauda exposed to Cu (Kováčik et al. 2010) C. pyrenoidosa with perfluorooctanoic acid exposure (Xu et al. 2013), S. obliquus exposed to Cu (Chen et al. 2012) and carbamazepine (Zhang et al. 2012), and C. vulgaris exposed to Cr (Rai et al. 2013) and dichloromethane and dichloroethane (Wu et al. 2014). In the present study, Cd(II) stress could damage the biosynthesis of chlorophyll in C. vulgaris, which is in agreement with results of Küpper et al. (2003), Rai et al. (2013), and Çelekli et al. (2016). The increase of Chlorophyll a/b suggesting that the Chl b is more sensitive than Chl b under 0.5 mg L−1, the decrease suggesting that cadmium can cause some Chl a to be converted to Chl b by oxidation of the methyl group on the ring II (Chettri et al. 1998).
The Carotenoid also decreased, Cd(II) ions had an adverse effect on the total carotene content. An adverse effect was previously reported for the carotene production by Ulva prolifera, U. linza (Jiang et al. 2013) and S. setiformis (Çelekli et al. 2016) under Cd(II) exposure.
The soluble protein content increased under Cd(II) stress. The increase of soluble protein is because of soluble protein is related to a variety of metabolic processes in cells, heavy metal stress can induce related stress protein gene expression, which is a defense mechanism of plants to environment stress (Xu et al. 2007).
Cd(II) stress enhanced the accumulation of hydrogen peroxide and superoxide anion in C. vulgaris. Increasing hydrogen peroxide and superoxide anion content of algae due to exposure of heavy metal has been previously studied by many researchers (Wu et al. 2014; Çelekli et al. 2016). One of the mechanisms that was involved in the prevention of metal-induced cell destruction has been the synthesis of antioxidative enzymes (Wu and Lee 2008). Elevated levels of antioxidant enzymes SOD, CAT, GR and POD in C. vulgaris following the Cd treatment in this study indicated that these enzymes could act in combination to reduce the impact of metal toxicity, the same results has reported in Acanthophora spicifera, Chaetomorpha antennina, and Ulva reticulate (Babu et al. 2014).
A concentration-dependent increase in antioxidant activity was observed in the present work, similar to the reported results in C. vulgaris (Bajguz 2010). Increased glutathione levels had been shown to correlate with plant adaptation to extreme metal stress, and decreased glutathione pool shows marked alterations in response to metal stress (Jin et al. 2008; Masood et al. 2012). Therefore, the increased glutathione level noted in C. vulgaris when treated with Cd under 0–1 mg L−1, that may precede phytochelatin accumulation by intracellular sequestration of metal ions (De Vos et al. 1992). And the decreased glutathione level showed in C. vulgaris when treated with Cd under 3–7 mg L−1, similarly, exposure of Cd decreased glutathione of A. spicifera and exposure of Cu decreased glutathione of C. antennina (Babu et al. 2014).
Induction of SOD activity in plant cells had been correlated with increased tolerance to a variety of chemical compounds and physical stresses (Mittler 2002). Induced SOD activity can either be due to the increased production of ROS or the protective measure adopted by macroalgae against oxidative damage. CAT is one of the key enzymes involved in the removal of toxic peroxides as it quenches H2O2 to water and molecular oxygen. In the present study, the increase in CAT activity can be considered as an adaptive mechanism developed by plants (Reddy et al. 2005). Reduction of CAT activity observed at the higher concentration of metals might be attributed to inactivation of enzyme by ROS, decrease in synthesis of enzyme, or change in the assembly of its subunits (Verma and Dubey 2003). POD also plays an important role in respiratory metabolism in plants. In the present study, the activity of POD increases with the increasing cadmium concentration until 5 mg L−1 and then begins to decrease.
Pollution in aquatic environments by metals has received considerable attention. Pollution of aquatic environments with heavy metals from natural water is a serious problem because of the toxicity of heavy metals to humans, fish and other live organisms. For this reason, pollution impact studies that focus on the aquatic environment are receiving more attention. This study confirmed that C. vulgaris showed a remarkable response to Cd(II) stress. Cadmium stress caused a variety of toxicity to C. vulgaris, such as algal biomass, chlorophyll, protein content decreased, H2O2 and O 2 ·− content increased. But C. vulgaris can adapt and regulation by changing the activity of SOD, POD, CAT and GR when subjected to cadmium stress in environment, thereby increasing the resistance to cadmium stress of C. vulgaris. Our research found that C. vulgaris has a high tolerance to cadmium. Hence, regulatory measures have to be taken by the authorities to limit the concentration of metal pollutants in the aquatic environment. This study also shows a range of physiological responses measured in this green alga under Cd(II) stress could be used as natural biomarkers or bioindicators of Cd contaminations in contaminated aquatic ecosystems.
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JFC participated in the design of the study, and performed the statistical analysis. JRG and KWY performed the experiments. HCQ and ZYC helped to revise the manuscript. All authors read and approved the final manuscript.
This study was supported by the National Natural Science Foundation of China (31000099), the Fundamental Research Funds of the Northwest A&F University (2014YB038).
The authors declare that they have no competing interests.
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Cheng, J., Qiu, H., Chang, Z. et al. The effect of cadmium on the growth and antioxidant response for freshwater algae Chlorella vulgaris . SpringerPlus 5, 1290 (2016) doi:10.1186/s40064-016-2963-1
- Chlorella vulgaris
- Reactive oxygen species (ROS)
- Antioxidant enzymes