- Research article
- Open Access
Bioaccumulation and toxicity of selenium compounds in the green alga Scenedesmus quadricauda
- Dáša Umysová†1,
- Milada Vítová1Email author,
- Irena Doušková†1,
- Kateřina Bišová1,
- Monika Hlavová1,
- Mária Čížková1,
- Jiří Machát2,
- Jiří Doucha1 and
- Vilém Zachleder1
© Umysová et al; licensee BioMed Central Ltd. 2009
Received: 12 November 2008
Accepted: 15 May 2009
Published: 15 May 2009
Selenium is a trace element performing important biological functions in many organisms including humans. It usually affects organisms in a strictly dosage-dependent manner being essential at low and toxic at higher concentrations. The impact of selenium on mammalian and land plant cells has been quite extensively studied. Information about algal cells is rare despite of the fact that they could produce selenium enriched biomass for biotechnology purposes.
We studied the impact of selenium compounds on the green chlorococcal alga Scenedesmus quadricauda. Both the dose and chemical forms of Se were critical factors in the cellular response. Se toxicity increased in cultures grown under sulfur deficient conditions. We selected three strains of Scenedesmus quadricauda specifically resistant to high concentrations of inorganic selenium added as selenite (Na2SeO3) – strain SeIV, selenate (Na2SeO4) – strain SeVI or both – strain SeIV+VI. The total amount of Se and selenomethionine in biomass increased with increasing concentration of Se in the culturing media. The selenomethionine made up 30–40% of the total Se in biomass. In both the wild type and Se-resistant strains, the activity of thioredoxin reductase, increased rapidly in the presence of the form of selenium for which the given algal strain was not resistant.
The selenium effect on the green alga Scenedesmus quadricauda was not only dose dependent, but the chemical form of the element was also crucial. With sulfur deficiency, the selenium toxicity increases, indicating interference of Se with sulfur metabolism. The amount of selenium and SeMet in algal biomass was dependent on both the type of compound and its dose. The activity of thioredoxin reductase was affected by selenium treatment in dose-dependent and toxic-dependent manner. The findings implied that the increase in TR activity in algal cells was a stress response to selenium cytotoxicity. Our study provides a new insight into the impact of selenium on green algae, especially with regard to its toxicity and bioaccumulation.
Selenium is a trace element, which affects organisms in a dose-dependent manner. At low levels, it contributes to normal cell growth and function. It has a anti-carcinogenic effect [1–3], plays a role in mammalian development , immune function , and in slowing down aging . On the other hand, high concentrations are toxic, causing the generation of reactive oxygen species (ROS), which can induce DNA oxidation, DNA double-strand breaks and cell death .
In algae, the essentiality of selenium has been studied mainly in marine species. Selenite bioconcentration by phytoplankton  and selenium requirements of many of phytoplankton species from various taxons was demonstrated . Unicellular, marine calcifying alga Emiliania huxleyi requires nanomolar levels of selenium for growth and selenite ion is the predominant species used by this alga . Se is essential to many algae  including Chlamydomonas reinhardtii . The essentiality, however, is sometimes difficult to estimate because selenium is required at such low levels for most organisms that it is experimentally challenging to generate strong phenotypes of deficiency .
The function of selenium is mediated mostly by selenoproteins, to which the selenium as a selenocysteine is inserted during translation [14, 15]. Selenoproteins include enzymes such as glutathione peroxidases (GPx), thioredoxin reductases (TR), proteins implicated in the selenium transport (selenoprotein P) and proteins with unknown functions, which are involved in maintaining the cell redox potential .
Most of the selenoproteins are found as animal proteins. They have not been found in yeast and land plants. Surprisingly, they have been detected in the green alga Chlamydomonas reinhardtii. Chlamydomonas uses selenoenzymes and the repertoire is almost comparable to that in mammalian models . A survey of the Chlamydomonas genome led to the identification of the complete selenoproteome defined by 12 selenoproteins representing 10 families [17, 18]. The unicellular alga Ostreococcus (Prasinophyceae) and ultra small unicellular red alga Cyanidioschyzon (Cyanidiaceae) also use selenoenzymes [19–21] as well as Emiliania huxleyi (Haptophytes) . Among these selenoenzymes, one of the form of thioredoxin reductase (TR) was also identified . The thioredoxin system, comprising thioredoxin (TRX), TR and NADPH works as a general protein reductase system .
In the cytosol and the mitochondria, thioredoxins are reduced by NADPH through the NADPH thioredoxin reductase (NTR) present in these compartments. NTR is universally distributed from bacteria to mammals, but two different forms have evolved. The first corresponds to a low molecular weight NTR found in bacteria, yeast, and plants. Mammals contain a distinct form of NTR, which contains selenocysteine .
Of the 4 NTRs found in Chlamydomonas, one of them was quite unexpected since it is a mammalian type NTR containing a selenocysteine residue [15, 16]. This NTR is also encoded in another alga, Ostreococcus, but not in land plants . Some authors showed that TR provides active selenide for the synthesis of selenoproteins and is an important protector of cells against Se toxicity [26–28].
Besides the presence of selenium in selenocysteine, selenium can substitute sulfur in methionine and form selenomethionine. This can be incorporated nonspecifically into proteins instead of methionine. This misincorporation may result in significant alterations in protein structure and consequently protein function causing a toxic effect of Se in land plants .
In model algal organisms, studies of the effects of both selenite and selenate on the green alga Chlamydomonas reinhardtii showed ultrastructural damage to chloroplasts resulting in impaired photosynthesis [30, 31]. In C. reinhardtii selenite is transported by a specific rapidly saturated system at low concentrations and non-specifically at higher concentrations . Fluxes for selenite uptake were constant, while fluxes for selenate and SeMet uptake decreased with increasing concentrations, suggesting a saturated transport system at high concentrations . In Scenedesmus obliquus, phosphate enrichment leads to considerable decrease of Se accumulation . In Chlorella zofingiensis the accumulation of boiling-stable proteins and the increased activities of the antioxidant enzymes suggested that these compounds were involved in the mechanisms of selenium tolerance .
Here, we studied the response of the wild type of the green alga Scenedesmus quadricauda and its three selected strains to the presence of selenite and selenate of different concentrations. Strains were selected to be resistant to high doses of selenite or selenate or both. To monitor cellular response, we followed the growth rate, the total amount of Se and selenomethionine in algal biomass and the activity of thioredoxin reductase. The effect of the presence of selenium compounds in cultures deprived of sulfur was also studied.
Results and discussion
Toxicity of selenium and selection of selenium resistant strains
In contrast to Scenedesmus, no adaptation mechanisms were observed in Chlamydomonas. The authors found that chloroplasts were the first target of selenite cytotoxicity, with effects on the stroma, thylakoids and pyrenoids. At higher concentrations, they observed an increase in the number and volume of starch grains and electron-dense granules containing selenium .
The present findings confirmed the diverse effect of selenite and selenate on the cells, which is probably caused by distinct mechanisms of uptake and further metabolisms of different Se compounds as found in land plants and Cyanobacteria [38, 39]. Selenate is accumulated in land plant cells against its likely electrochemical potential gradient through a process of active transport . Selenate readily competes with the uptake of sulfate and it has been proposed that both anions are taken up via a sulfate transporter in the root plasma membrane in land plants. Selenate uptake in other organisms, including Escherichia coli , yeast  and Synechocystis sp.  is also mediated by a sulfate transporter .
Selenite uptake was significantly lower than selenate uptake in willow . However, the sensitivity of algae to the element has been shown to be highly species-dependent. For instance, it was found that concentrations of selenate inhibiting growth could vary as much as three orders of magnitude depending on the species tested . Moreover, natural phytoplankton communities could be more sensitive than single species, grown in optimal conditions in the laboratory .
Unlike selenate, there was no evidence that the uptake of selenite is mediated by membrane transporters. The mechanism of selenite uptake by plants remains unclear. Recently, selenite uptake in wheat has been found to be an active process likely mediated, at least partly, by phosphate transporters. Selenite and selenate differ greatly in the ease of assimilation and xylem transport . Selenate assimilation follows, in principle, that of sulfate and leads to the formation of SeCys and SeMet. Selenite is reduced to selenide and then forms selenoaminoacids .
We found that selenite was more toxic than selenate and caused more severe growth inhibition, which is in line with findings in land plants. This might be due to the faster conversion of selenite to selenoaminoacids in the species studied . On the other hand, selenate was reported to be more toxic than selenite and caused more severe growth inhibition in grass species .
Growth of sulfur deficient cells in the presence of selenite
Selenium and sulfur content in biomass of Scenedesmus quadricauda
Selenite mg Se × l-1
Selenium mg/kg D.W.
Sulfur mg/kg D.W.
With a further decrease of sulfur concentrations (4 mM and 0.4 mM), the growth rate of cells as well as the interval of growth progressively decreased (Figures 3A and 3C). The total sulfur content in biomass also decreased; it was not even possible to obtain an appropriate amount of biomass for analyses at 0.4 mM sulfate, as the culture grew so poorly (Table 1).
The growth of sulfur deficient cells in the presence of selenite was more affected than in its absence both in the wild type (Figures 3B and 3E) and selenite resistant strain (Figures 3D and 3F). The total selenium content in biomass was, however, independent of sulfate concentration and was proportional to selenium concentration in the nutrient solution (Table 1).
The increasing selenium toxicity with sulfur deficiency indicates interference of Se with sulfur metabolism, possibly resulting from non-specific replacement of sulfur by selenium in proteins and other sulfur compounds. In land plants, Se toxicity is associated with the incorporation of selenocystein (SeCys) and selenomethionine (SeMet) into proteins in place of Cys and Met. The differences in size and ionization properties of S and Se may result in significant alterations in structure and consequently function of proteins .
Amount of intracellular selenium and selenomethionine
Percentage of selenomethionine in a total cellular Se in wild (WT) and selenium resistant strains (SeIV, SeVI, SeIV+VI) of Scenedesmus quadricauda grown in the presence of selenite or selenate
Se mg × kg-1
of cellular Se
All strains grown in the absence of selenium possessed a very low amount of intracellular Se and SeMet. Increasing the Se concentration added both in form of selenite and selenate caused a dose-dependent increase of the total content of Se and SeMet in the wild type. In the presence of selenate 50 mg Se × l-1 in media, the SeMet content reached 300 mg × kg-1.
In the selenite resistant strain SeIV, the total Se content and SeMet was low (20 – 40 mg × kg-1) in the presence of selenite. In contrast, the presence of selenate caused the total Se content to increase markedly above 850 mg × kg-1and was even higher than in the wild type. The finding that the SeIV strain treated with selenite has much lower levels of total Se and SeMet shows that its tolerance mechanism is probably exclusion. Its Se and SeMet levels are similar to the wild type when treated with selenate, explaining its lack of selenate tolerance and also showing that selenate and selenite are imported in this alga by different mechanisms.
In the selenate resistant strain SeVI, the presence of selenate caused a moderate increase in Se (up to 600 mg × kg-1) and SeMet content (up to 160 mg × kg-1). The presence of selenite increased the Se (800 mg × kg-1) and SeMet (210 mg × kg-1) content markedly. The SeVI strain shows no difference from WT in terms of total Se and SeMet levels, indicating that its tolerance mechanism is not exclusion but must be something internal, a way to detoxify or sequester the Se intracellularly.
The double-tolerant strain (SeIV+VI) has exceptionally low SeMet fractions (up to 50 mg × kg-1) compared to the other strains, which could indicate a change in Se metabolism, perhaps reduced assimilation from inorganic to organic Se.
Our results indicate that the increase of SeMet amount in the cells was correlated to toxicity of a given type of the added inorganic Se compound. The amount of selenium and SeMet in algal biomass was, in addition to its dependence on the type of the compound, also dose-dependent (compare bars of 20 and 50 mg Se × l-1 in Figure 4).
Papers dealing with the identification of selenium compounds in algae biomass are less frequent than those dealing with other systems. Several selenium compounds (dimethylselenopropionate, Se-allylselenocysteine, selenomethionine) were identified in the green alga Chlorella vulgaris . Selenomethionine was present only in ng × g-1 concentrations. In Chlorella treated with selenate and selenite the content of selenomethionine was determined using K-edge X-ray absorption spectroscopy . It comprised 39% and 24% of the accumulated Se when treated with selenite and selenate respectively. An effort to quantify Se compounds (fractionation) can be found in  dealing with selenized blue-green alga Spirulina platensis. Cultivation with selenite up to 40 mg Se × l-1 stimulated the growth of Spirulina. It was demonstrated that inorganic selenite could be transformed into organic forms. The organic selenium accounted for 85.1% of the total accumulated selenium and was comprised of 25.2% water-soluble protein-bound Se.
According to our results, the SeMet content (29% and 41%) in Scenedesmus quadricauda after incubation with selenite and selenate, respectively was comparable to the results obtained in Chlorella (24% and 39%) .
Activity of thioredoxin reductase
The initial TR activity in both wild type and resistant strains was the same at the beginning of the cell cycle (about 5 mU × mg-1). During the growth phase of the untreated wild type, the activity increased slightly and then declined gradually to a constant low level (Figure 7A, crosses). A similar pattern was observed also in resistant strains SeIV and SeVI, if grown in the presence of selenium compound(s) to which they were resistant (Figures 7B and 7C). In the wild type cultivated with 50 mg Se × l-1 as selenite or selenate, the activity increased extensively during the growth phase (up to 32 and 26 mU × mg-1 respectively) and persisted at a high level till the end of the cell cycle. The TR activity was higher in the presence of selenite than in the presence of selenate (Figure 7A). Similarly the TR activity increased in the strains SeIV and SeVI when grown in the presence of Se compounds, to which they were not resistant (33 mU × mg-1) (Figures 7B and 7C). In the case of strain SeIV+VI the TR activity was low (about 5 mU × mg-1) during the whole cell cycle (Figure 7D).
The present results indicate that the activity of thioredoxin reductase is affected by selenium treatment in both a dose-dependent and toxic-dependent manner. The more toxic the selenium forms for the given algal strain are, the higher the TR activity present. This indicates that the activity of TR in algal cells is a reaction to the toxic effect of selenium. This is in agreement with findings in mammalian cells, where increased resistance to selenium cytotoxicity in cells with high levels of active TR, was demonstrated . The authors concluded that a high level of active TR or a capacity to respond by inducing the expression of TR is a crucial mechanism for cells to survive exposure to sub-toxic/toxic levels of selenium compounds. TR over-expressing cells, which were preincubated for 72 h with 0.1 μM selenite, were significantly more resistant to selenite cytotoxicity than control cells .
TR is assumed to be an important enzyme in protecting against selenium cytotoxicity. The enzyme may protect cells against selenium cytotoxicity by at least three different mechanisms . One mechanism is the direct reduction and detoxification of hydroperoxides including lipid-hydroperoxides and hydrogen peroxide . The second mechanism involves reduction of thioredoxin and regeneration of antioxidants like ubiquinone . The third and maybe most important mechanism is restoration of intracellular thiols lost by oxidation and also reduction of selenite to elemental selenium with a comparably low toxicity .
Concerning the present results, the TR activity increased in the presence of toxic levels of selenium as it was found in mammalian cells. This would indicate a defensive response of algal cells to selenium toxicity but it can be also only a general reaction to stress without a direct relation to selenium.
Selenium toxicity in the wild type cells of the green alga Scenedesmus quadricauda increased with increasing dosage of selenium added as selenite or selenate. The selenium compounds caused cell growth inhibition as well as a block of cell division. Both of the compounds caused dose dependent accumulation of selenomethionine (SeMet), an organic form of selenium. Of the two compounds, selenite was more toxic than selenate. This was probably due to an increase of a selenomethionine (29% of SeMet in the case of selenate and 41% of SeMet in the case of selenite). The increasing toxicity was also accompanied by an increase in thioredoxin reductase (TR) activity implying a role for it in the stress response. Selenium toxicity increased in cultures grown under sulfur deficient conditions, indicating interference of selenium with sulfur metabolism. However, the total selenium content in biomass was proportional to selenium concentration in nutrient solution and independent of sulfate concentration.
We selected three strains resistant to high concentrations of different selenium compounds. The strains differed in the compound(s) to which they were resistant as well as in the degree of the resistance. The selected strains were resistant to selenite or selenate while still sensitive to the other compound. The strain resistant to combinations of both selenite and selenate showed the lowest resistance of all selected strains. This indicates that modes of action of selenite and selenate are different and modification of a common pathway for both compounds can provide only a limited degree of resistance. The selenite resistant strain (SeIV) showed very low levels of total selenium and its organic form selenomethionine if treated with selenite, implying that its resistance is caused by exclusion, probably due to downregulation of a sulfate transporter. Since its level of total selenium and selenomethionine are similar to wild type levels if treated by selenate the import mechanism for selenite and selenate seem to be different. On the contrary, the selenate resistant strain (SeVI) had the same levels of both total selenium and selenomethionine in the presence of selenate. This indicates that the mechanism of resistance is not due to changes in the import level but rather to some unknown internal mechanism decreasing the selenium toxicity. Interestingly, to gain resistance to both selenate and selenite the cells probably modified the mechanism responsible for the conversion of selenium into its organic compound, selenomethionine. Therefore, it appears that there are at least three different and independent mechanisms able to establish resistance to selenium compounds.
In wild type and all the resistant strains the addition of a toxic form of selenium for a particular strain was accompanied with an increase in the activity of thioredoxin reductase (TR). The TR activity was affected in dose-dependent and toxic-dependent manner. The more toxic the selenium form for the given algal strain, the higher the TR activity found. This indicates that TR activity is either one of the hallmarks of stress caused by selenium (or general stress) and/or, more appealingly, it is actively involved in detoxification of selenium as indicated in the literature.
The study provides a new insight into the impact of selenium on green algae with reference to its toxicity and bioaccumulation. Selenium is an essential micronutrient in the diet of many organisms, including humans and significant health benefits have been attributed to it. Selenomethionine is, due to its enhanced bioavailability, essential both in biomedicine and to complement the diet of domestic animals. The enrichment of the selenate resistant strains in selenomethionine could be scaled up to produce selenium enriched algal biomass. Also, the selected selenium resistant strains could be used for bioremediation of selenium-contaminated surroundings.
Experimental organism, culture growth conditions
The chlorococcal alga Scenedesmus quadricauda (TURP.) BRÉB. Strain Greifswald/15 was obtained from the Culture Collection of Autotrophic Microorganisms (Institute of Botany, Třeboň, Czech Republic). The species belongs the algae, which are able to divide by multiple fission into more than two daughter cells connected in coenobia. Actually 2-, 4-, or 8-celled coenobia can be formed. The cells are firmly connected in coenobium for the whole cell cycle. Marginal cells of the coenobium (not inner ones) are ornamented by two projecting spines, which are a part of the cell wall consisting of sporopollenin and are typical for the species. Cultures of S. quadricauda were cultivated at 30°C in liquid mineral medium  in a laboratory-scale photobioreactor. The cultures were aerated with air containing 2% carbon dioxide (v/v). The photobioreactor was illuminated from one side by fluorescent lamps (Osram DULUX L, 55 W/840, Italy) at an incident radiance of 100 W × m-1 (400–720 nm) at the surface. To obtain synchronized cells, the cultures grown at alternating light and dark periods (14:10 h).
The selenium was added as selenite or selenate in the range of concentrations (5 – 400 mg Se × l-1) to nutrient medium at the beginning of cultivation. Three replicate samples were used for all analyses and measurements. The average value was used for the construction of graphs. Standard deviations were indicated as bi-directional bars.
Determination of total Se content (ICP-MS)
Nitric acid (65%, p.a., Merck Darmstadt, Germany) and hydrogen peroxide (30%, Analpure, Analytika Prague, Czech Republic) were used in the mixture used to digest biomass for the determination of total Se. A sample (0.1 g) of biomass was digested with 4 ml of nitric acid and 2 ml of hydrogen peroxide at 190°C in a PTFE vessel in a closed microwave digestion system (Berghof, Germany). After evaporation of excess acid in the same MW system, the resulting solution was transferred to a volumetric flask (100 ml) and filled with water (18.2 MΩ resistivity, Millipore Simplicity, Bedford, MA, USA).
An Inductively coupled plasma – mass spectrometer Agilent 7500ce (Agilent Technologies, Japan) was used for analysis of sample solutions. For quantification of Se, a standard addition method was used to eliminate matrix effects of residual carbon and other matrix elements. Se isotopes 77 and 82 were used, as these isotopes did not suffer from Ar-based spectral interferences. All data are presented as means ± S.D. of five experiments.
Determination of SeMet content (ICP-MS)
Methanesulfonic acid hydrolysis of proteins in biomass was applied in the determination of total SeMet content in biomass according to. 100 mg of algal biomass (dry weight) was mixed with 10 ml of methanesulfonic acid (4 mol × l-1, Sigma-Aldrich, Prague, Czech Republic) and 0.2 ml 2-mercaptoethanol (Fluka, Prague, Czech Republic) and refluxed for 16 hours. The resulting solution was filled to 100 ml with deionized water and filtered through a 0.45-μm syringe filter (regenerated cellulose) prior to chromatographic analysis.
For the separation of Se species, anion-exchange chromatography with ICP-MS detection was applied. A strongly basic anion exchange column Hamilton PRP-X100 (4.6 × 150 mm + 4.6 × 25 mm guard column, Hamilton Company, Nevada, USA) was operated in isocratic mode with ammonium acetate/methanol mobile phase [pH 5.0, 40 mM, 1% v/v methanol, 0.6 ml × min-1] at 25°C. Se species were detected using Se isotopes 77 and 82. Selenomethionine (> 99%, Sigma-Aldrich, Prague, Czech Republic) standard solutions in methanesulfonic acid were used for calibration. All data are presented as means ± S.D. of five experiments.
Enzyme activity assay
Thioredoxin reductase (TR) activity was determined by the method according to (Holmgren and Bjőrnstedt, 1995). Cells were centrifuged at 4000 rpm for 5 minutes, washed with buffer A [50 mM Tris/HCl, 1 mM EDTA, pH 7.5] and disintegrated by vortexing with zircon beads (diameter 0.7 μm, Biospec, Bartlesville, OK, USA) 2:1 in buffer A with plant protease inhibitors (Sigma-Aldrich, Prague, Czech Republic) for 6 minutes. The extract was centrifuged at 13 000 rpm for 15 minutes and the supernatant frozen in liquid nitrogen. Cell extract (10 μl) was mixed with 490 μl of buffer A containing 2 μM Trx (E. coli, Sigma-Aldrich, Prague, Czech Republic), 500 μg × ml-1 insulin (bovine pancreas, Sigma-Aldrich, Prague, Czech Republic) and 200 μM NADPH (tetrasodium salt, Calbiochem, San Diego, CA, USA). The mixture was incubated at 37°C for 20 minutes. Reaction was terminated by addition of 500 μl of 6 M guanidine hydrochloride (Sigma-Aldrich, Prague, Czech Republic) containing 1 mM 5,5'-dithiobis (2-nitrobenzoic acid) (DTNB, Sigma-Aldrich, Prague, Czech Republic). The increase in spectrophotometric absorbance at 412 nm was read from a microtitre plate using an Infinite F200 spectrophotometer (TECAN, Mannendorf, Switzerland). Reaction without cell extract and reaction with pure TR (E. coli, Calbiochem, San Diego, CA, USA) in place of cell extract were used as negative and positive controls, respectively. Specific activity of the enzyme was expressed as units per mg protein, where 1 unit is defined as the amount of enzyme that will cause an absorbance change of 1 at 415 nm using 200 μM NADPH per min. Total cell protein concentration was determined using Bradford methods . All data are presented as means ± S.D. of triplicate experiments.
Cell size and number measurements
Cells were immediately fixed by glutaraldehyde (2% v/v). Fixed cells with densities ranging from 1 × 106 to 1 × 107 cells × ml-1 were diluted in 10 ml electrolyte solution [0.9% NaCl]; cell concentrations and cell size distributions were determined using a Coulter Multisizer III (Coulter Corporation, Florida, USA).
Observations in transmitted light and fluorescence microscopy were carried out using a BX51 microscope (Olympus, Japan) equipped with DIC (Differential interference contrast) and a U-MWIG2 filter block (excitation 520 – 550 nm, emission 580 nm). The microphotographs were taken using a CCD camera (F-View II).
This work was supported by the Grant Agency of ASCR (grant no. A600200701), projects EUREKA of Ministry of Education, Youth and Sports of the Czech Republic (no. OE221 and OE09025) and by Institutional Research Concept no. AV0Z50200510.
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