In vitro Cr(VI) reduction by cell-free extracts of chromate-reducing bacteria isolated from tannery effluent irrigated soil

• Published in: Environmental science and pollution research international 2013-03, Vol.20 (3), p.1661-1674
• Main Authors: Soni, Sumit K., Singh, Rakshapal, Awasthi, Ashutosh, Singh, Mangal, Kalra, Alok
• Format: Article
• Language: English
• Subjects: Aquatic Pollution; Atmospheric Protection/Air Quality Control/Air Pollution; Bacillus - genetics; Bacillus - metabolism; Bacillus subtilis; Bacillus subtilis - genetics; Bacillus subtilis - metabolism; Bacillus thuringiensis; Bacillus thuringiensis - genetics; Bacillus thuringiensis - metabolism; Bacteria; Base Sequence; Biodegradation, Environmental; Chromates; Chromates - metabolism; Chromium; Chromium - metabolism; Culture media; DNA methylation; Earth and Environmental Science; Ecotoxicology; Effluents; Environment; Environmental Chemistry; Environmental Health; Environmental science; Enzymes; Free radicals; Gene expression; Hydrogen-Ion Concentration; In Vitro Techniques; In vitro testing; Microbacterium; Microorganisms; Molecular Sequence Data; Phylogeny; Reduction; Research Article; RNA, Ribosomal, 16S - genetics; Soil contamination; Soil Microbiology; Soil Pollutants - analysis; Strain; Studies; Tanneries; Tannery wastes; Tanning; Temperature; Toxicity; Urea; Waste Water Technology; Water Management; Water Pollution Control
• ISSN: 0944-1344; 1614-7499
• DOI: 10.1007/s11356-012-1178-4

Four efficient Cr(VI)-reducing bacterial strains were isolated from rhizospheric soil of plants irrigated with tannery effluent and investigated for in vitro Cr(VI) reduction. Based on 16S rRNA gene sequencing, the isolated strains SUCR44, SUCR140, SUCR186, and SUCR188 were identified as Bacillus sp. (JN674188), Microbacterium sp. (JN674183), Bacillus thuringiensis (JN674184), and Bacillus subtilis (JN674195), respectively. All four isolates could completely reduce Cr(VI) in culture media at 0.2 mM concentration within a period of 24–120 h; SUCR140 completely reduced Cr(VI) within 24 h. Assay with the permeabilized cells (treated with Triton X-100 and Tween 80) and cell-free assay demonstrated that the Cr(VI) reduction activity was mainly associated with the soluble fraction of cells. Considering the major amount of chromium being reduced within 24–48 h, these fractions could have been released extracellularly also during their growth. At the temperature optima of 28 °C and pH 7.0, the specific activity of Cr(VI) reduction was determined to be 0.32, 0.42, 0.34, and 0.28 μmol Cr(VI) min −1  mg −1 protein for isolates SUCR44, SUCR140, SUCR186, and SUCR188, respectively. Addition of 0.1 mM NADH enhanced the Cr(VI) reduction in the cell-free extracts of all four strains. The Cr(VI) reduction activity in cell-free extracts of all the isolates was stable in presence of different metal ions tested except Hg 2+ . Beside this, urea and thiourea also reduced the activity of chromate reduction to significant levels.