The use of microorganisms to remove heavy metals from industrial effluent is an area of extensive research and development. Attempts have been made to isolate and characterize metal-resistant microorganisms from treated oil mill industry effluent wastewater samples. The metal-resistant organisms that showed values of minimum inhibitory concentration towards metals (Cd, Cr, Ni and Pb) ranging from 100 to 800 ppm level were screened. A potent metal-resistant organism, isolate BC15 from the wastewater samples was tentatively identified as Pseudomonas sp. Detailed analysis of morphological, biochemical and 16S rDNA sequence of the isolate revealed that it is closely related to Pseudomonas aeruginosa (94%). Pseudomonas BC15 was capable of absorbing 93% Ni, 65% Pb, 50% Cd and 30% Cr within 48 h from the medium containing 100 mg of each heavy metal per liter. The multiple metal tolerance of this strain was also associated with resistance to antibiotics such as ampicillin, tetracycline, chloramphenicol, erythromycin, kanamycin and streptomycin.
AB STRACT:The isolate Pseudomonas aeruginosa exhibited resistance to heavy metals such as cadmium, chromium, nickel and lead. Plasmid DNA was isolated from P. aeruginosa and designated as pBC15. The size of the plasmid DNA was approximately 23 kb. Escherichia coli DH5α was transformed with plasmid pBC15 subsequired resistance to nickel and ampicillin. The same size of the plasmid was isolated from E. coli transformant and separated on 0.7 % agarose gel electrophoresis. The restriction analysis of pBC15 showed that the plasmid DNA has single site for Bam HI and Eco RI and three sites for Xho I which were compared with 1 Kb DNA and λ Hind III digest molecular markers. Therefore, the size of the plasmid DNA of pBC15 was confirmed to be 23 kb. Curing was carried out by ethidium bromide, acridine orange, novobiocin, sodium dodechyl sulphate and elevated temperature (40 °C). Transformation and curing results suggest that nickel and ampicillin resistance gene was conferred by plasmid DNA. Cadmium resistant gene was present on chromosomal DNA along with the gene for chromium resistance. Lead resistance gene was shown to be present on the chromosomal DNA rather than the plasmid DNA as the cured and uncured cultures remained similar in lead resistance. Therefore, the ability of P. aeruginosa resistant to nickel and ampicillin is plasmid mediated and transferable to other strains whereas cadmium, chromium and lead could be chromosomal encoded. The heavy metal and antibiotic resistances of P. aeruginosa can be used to exploit for clean up industrial wastewater and bioremediation of heavy metal contaminated soil.
ABSTRACT:Environmental contamination by heavy metals is a worldwide problem. Therefore, it is necessary to develop sensitive, effective and inexpensive methods, which can efficiently monitor and determine the level of hazardous metals in the environment. Conventional techniques to analyze metals, suffer from the disadvantages of high cost. Alternatively, development of simple system for monitoring heavy metals pollution is therefore needed. The present approach is based on the use of bacteria that are genetically engineered so that a measurable signal is produced when the bacteria are in contact with the bioavailable metal ions. Reporter genes are widely used as genetic tools for quantification and detection of specific cell population, gene expression and constructing whole cell biosensors as specific and sensitive devices for measuring biologically relevant concentrations of pollutants. An attempt has been made to construct the reporter gene enhanced green fluorescent protein and was expressed under the control of cadR gene, responsible for cadmium resistance. Recombinant strain Escherichia coli cadR30 was used, that carried cadR gene in pET30b expression vector and cloned. Clones confirmed by the expression of enhanced green fluorescent protein was detected under ultraviolet illumination and separated on sodium dodecyl sulfate polyacrylamide gel electrophoresis. The construction of green fluorescent protein based Escherichia coli bacterial biosensor was developed based on green fluorescent protein expression under the control cadR gene of Pseudomonas aeruginosa BC15. The constructed bacterial biosensor is useful and applicable in determining the availability of heavy metals in soil and wastewater.
Boron is known to be widespread environmental contaminant that is relatively mobile in soil when compared to other metal contaminants. The present study made an attempt to isolate and characterize the boron resistant and accumulating bacteria from former mining site at Hokkaido, Japan. Four potential strains M1, M2, M3 and M4 were selected based on high degree of boron and heavy metal resistances. The morphological, biochemical and 16S rDNA sequencing analysis of mining bacteria revealed that the isolates were highly homology to Lysinibacillus fusiformis M1 (99 %), Bacillus cereus M2 (99 %), Bacillus cereus M3 (99 %) and Bacillus pumilus M4 (99 %) respectively. The strains M1, M2, M3 and M4 showed resistance to several heavy metals such as As (III), As (V) and Cr (VI), Cu, Ni, Pb and Zn. The selected strains were found to be arsenic oxidizing bacteria confirmed by Silver nitrate test. The resting and growing cells of mining bacteria were used for boron accumulation analysis. Selected strains were found to be efficiently accumulating boron concentration ranging from 0.1-2.3 mg L (-1) and 1.5-4.7 mg L (-1) at 24 h and 168 h, respectively. The following results conclude that the mining bacteria act as potent bioaccumulator of boron and its resistant, removal characteristic can be valuable in boron bioremediation.
Arsenic (As) is a toxic metalloid, having both properties of a metal and a non-metal. Boron (B) is a nonmetal, essential micronutrient for plants growth and development but its excess can be toxic to plants with various levels. In this study arsenic, boron and salt resistant bacteria were isolated from desert soil, Mongolia. The bacterial screening was carried out by serial dilution method. One hundred colonies were screened initially using of (2 mM) arsenic and (2 mM) boron containing LB agar medium. From this population, 10 bacterial isolates were selected based on arsenic and boron resistance, boron accumulation, salt tolerance and arsenic oxidizing capability. One of the potent strain, MS 11 from Mongolia desert soil, was tentatively identified as Bacillus sp. The phylogenetic and comparative analysis of 16S rRNA gene sequence with closely related validly published species available in the database showed that the isolate MS11 was closely related to Bacillus safensis FO-036b(T) with the highest sequence similarity (99.439%). The 16S rRNA gene sequence of the strain MS11 was submitted in the NCBI database with the accession number JF836885. B. safensis MS11 exhibited high level of resistance to arsenite (40 mM), arsenate (400 mM), boron (200 mM) and 15% salt tolerance in LB agar medium. B. safensis MS11 was also associated with resistance to multiple heavy metals such as Cd, Cr, Cu, Ni, Pb and Zn. Hence, this bacterium could be useful in the remediation of salt affected soils and biogeochemical cycles of arsenic pollution.
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