Research Article
Selective Bioaccumulation of Mixed Heavy Metals by a Range of Brackish Water Bacteria
Department of Environmental Studies, Institute of Graduate Studies and Research, University of Alexandria, Alexandria, Egypt
Microorganisms mediate many important processes in the aquatic environment including self-purification from (different pollutants including heavy metals) and nutrient recycling. The development of heavy metals tolerance by the microbial community would allow the maintenance of these important processes despite the heavy metals inputs to the environment. Development of heavy metals tolerance in microorganisms can be done by different means, one of which is to subject the microorganisms to a gradual increase in metal concentration over a period of time (Sakamoto et al., 1989; Kai et al., 1995).
The removal and recovery of heavy metals from contaminated aqueous systems by microorganisms have several advantages: (1) microbial cells have a high metals adsorbing ability (2) they can absorb metals selectively (3) they produce microbial biomass inexpensively (4) both their growing and immobilized cells have the ability to accumulate metals (5) they pose no disposal problems and (6) they can accumulate metals very rapidly (Nakajima and Sakaguchi, 1986).
Microorganisms posses highly specific metal transport systems, thus they can selectively accumulate certain metals (Macaskie and Dean, 1989; Beveridge, 1989; Kim et al., 1995). Some microorganisms Survive the presence of elevating levels of heavy metals by employing detoxification mechanisms and developing tolerance (Timoney, 1989; Rouch et al., 1989; Schreiber et al., 1990). Examples of positive and negative effects of some of the investigated heavy metals on metabolic activities of microbial cells were discussed including Fe (Abeck et al., 1990; Nakajima and Sakaguchi, 1986; Paerl et al., 1994), Cu (Erardi et al., 1987; Harwood-Sears and Gordon, 1990; Collins et al., 1991), Zn and Ni (Fang and Hui, 1994) and Pb (Leborans et al., 1998).
The present study is a continuation of a series of studies on the bioremediation of heavy metals from contaminated effluents using naturally occurring bacteria isolated from brackish water. It was started by an investigation on the role of bacteria and phytoplankton in the cycling of pollutant metals in L. Mariut, Alexandria (El-Bestawy, 1993). This was followed by isolation and identification of bacteria with high ability for metals accumulation (Amer, 1997). In the present study, seven of the most promising bacterial species in metal uptake were selected. The main objective is to investigate their selectivity for metals uptake and to enhance their bioaccumulation capabilities by exposing them to a gradual increase in metal levels.
Microorganisms: Seven bacterial species originally isolated from heavily polluted brackish water of Lake Mariut, Alexandria were selected for this investigation. They were previously identified as Bacillus cereus, B. alvei, B. licheniformis, Staphylococcus aureus, Pseudomonas cepacia, Enterobacter agglomerans and E. coli (Amer, 1997). The selected bacterial proved to exhibit high ability for metals uptake.
Metals bioaccumulation assays: Metals bioaccumulation by the selected bacteria was determined at three elevating metal-concentrations (Table 1).
Stock solutions of the investigated metals (Fe, Zn, Cu, Co, Pb and Ni) were prepared from chloride salts in de-ionized water and sterilized by filtration through 0.22 millipore membrane filter. Each of the selected species was inoculated in 100 nutrient broth medium (NB), incubated at 37°C and agitated at 120°C rpm for 3 hrs to get into the early log phase of growth before the addition of metals. Metals were then added to bacterial cultures and incubated at the same growth condition. After 6-hr exposure, 10 ml samples of each bacterial cultures at the different metals levels in addition to control cultures were plated under aseptic conditions.
Bacterial cells were harvested by centrifugation at 8000 rpm, weighed and digested with concentrated nitric acid (AR grade) according to the Standard Methods for the examination of water and wastewater (Greenberg et al., 1995). Metals were then determined using atomic absorption spectrophotometer. The same procedure w as repeated after 18 hrs, then every 24 hrs for 5 successive days. For bacterial count samples including a control sample were taken, serially diluted and then inoculated onto nutrient agar plates.
Fig. 1: | Effect of mixed heavy metals on the growth of different bacterial species |
Fig. 2: | Levels of Ni accumulated by different bacterial species |
Fig. 3: | Levels of Zn accumulated by different bacterial species |
Fig. 4: | Levels of Fe accumulated by different bacterial species |
Fig. 5: | Levels of Co accumulated by different bacterial species |
Fig. 6: | Levels of Pb accumulated by different bacterial species |
Fig. 7: | Levels of Co accumulated by different bacterial species |
Table 1: | Concentrations of heavy metals used in the bioaccumulation assays |
Counting bacteria in each sample was carried out after 24 hr incubation at 37°C. |
Effect of metals concentration on the growth of bacterial species under investigation: The response of bacterial growth to metals varied according to the type of bacteria and to the metals concentration in the growth medium. The general trend of bacterial growth regardless metal concentration agrees with the normal bacterial growth curve (Dean-Ross and Mills, 1989), with few exceptions regarding Bacillus species. However, S. aureus was affected by metals concentration in the medium, where its growth was considerably suppressed by increasing metal concentration, which is an indication of the toxic effect of metals in the mixture against S. aureus.
Although, the same trend was recorded for P. capacia and E. agglomorans, it was noticed that P. capacia retained part of its capacity to grow in the presence of high metal concentration. This could be due to their the depletion of metals in the medium (Hughes and Poole, 1989), or to the acclimatization of the bacterial cells during the growth phases under a high concentration level of metals by different mechanisms such as, reducing metal uptake or a change in the intracellular distribution of ion within the cell (Joho et al., 1990; Podlesek et al., 1993).
However, E. coli, B. alvei and B. cereus showed tolerance to the metals used in this study even at higher concentrations. This indicates that these bacterial strains are metal resistant species and they can consider to be used in removing metals from growth media containing such metals (Fig. 1).
Accumulation of metals by the tested bacteria: Results of Ni accumulation (Fig. 2) indicated that bacterial cells in their early growth stages can accumulate Ni to a certain level, after which Ni accumulation decreased by increasing the incubation time. This could be due to a selective property (Nakajima and Sakaguchi, 1986), or due to a certain resistant mechanism that allow the bacterial cells to alter Ni accumulation (Stoppel and Schlegel, 1995). The previous trend was true for most of the tested bacteria except B. alvei and B. cereu.
The results of Zn accumulation (Fig. 3), indicated that Zn is an essential element for bacterial growth at it is accumulated at higher levels compared to other elements. This is in agreement with other results obtained by several authors (Hughes and Poole, 1989; Nies, 1992; Podlesek et al., 1993). Similar to Zn, most of the tested bacterial strains accumulated Fe as Zn at higher concentration levels (Fig. 4). This is attributed to the well-known role of both Zn and Fe in the metabolic activity of the bacterial cells (Abeck et al., 1990) especially as cofactors in the enzymatic activities (Lim, 1989).
The tested bacteria also showed tolerant property against Co (Fig. 5). The high accumulation level of Co within the bacterial biomass, at almost all tested concentrations indicated this. This could be attributed to the ability of such bacteria to utilize the toxic Co and/or to a resistant mechanism enabled the bacterial cells to tolerate such high concentration levels of Co (Klerks and Levinton, 1993; Dean-Ross and Mills, 1989).
Accumulation of lead (Pb) was almost similar to Co, except with B. licheniformis at the late stages of bacterial growth and partially with B. alvei and S. aereus at the highest Pb concentration. This could be due to the release of the bound Pb from the sensitive cells, but on the other hand Pb will remain attached to or within resistant cells (Levinson et al., 1996).
The trend of Cu accumulation in all tested bacterial cells was very pronounced. The level of Cu. Accumulation was very low, except for S. aereus at the late growth stages of the cells at the highest metal concentration. This could be due to the adaptation of this strain when grain under high concentration level of Cu, then a turnover in the accumulation expression allowed the cells to accumulate Cu in a considerable amount that exceeded the levels accumulated in the early growth stages by more than 6-fold. However, the low accumulation of Cu in bacterial cells is expected, where the accumulation of such metal could lead to the mortality of the exposed cells due to the known toxic effect of copper metal to biota generally and in specific to certain microorganisms (Cooksey, 1990; 1993) (Fig. 6).
The previous results indicated that the selected bacterial strains can be used as a good biosorbent for a range of metals in a mixed medium. This could be due to either its tolerant to such metals or to a certain resistant mechanism expressed itself when the bacteria grew under high metal stress. By the way, the growing cells exhibited properties that allowed them to accumulate metals at high rate including the toxic elements. This is proved by the level of bacterial populations (upto 106 cfu/ml) that were recorded at when the bacterial cells grew at different elevating levels of metals concentration. On the other hand, the trend of metal accumulation could be due to certain selective property gained by those bacteria to accumulate specific metal without being antagonized regardless the toxicity of some of the tested metals (Fig. 7).