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Reduction of Dissolved Fe(III) by As(V)-tolerant Bacteria Isolated from Rhizosphere Soil

  • Khanal, Anamika (Department of Bioenvironmental Chemistry, College of Agriculture & Life Sciences, Jeonbuk National University) ;
  • Song, Yoonjin (Department of Bioenvironmental Chemistry, College of Agriculture & Life Sciences, Jeonbuk National University) ;
  • Cho, Ahyeon (Department of Bioenvironmental Chemistry, College of Agriculture & Life Sciences, Jeonbuk National University) ;
  • Lee, Ji-Hoon (Department of Bioenvironmental Chemistry, College of Agriculture & Life Sciences, Jeonbuk National University)
  • Received : 2021.03.15
  • Accepted : 2021.03.25
  • Published : 2021.03.31

Abstract

BACKGROUND: Biological iron redox transformation alters iron minerals, which may act as effective adsorbents for arsenate [As(V)] in the environments. In the viewpoint of alleviating arsenate, microbial Fe(III) reduction was sought under high concentration of As(V). In this study, Fe(III)-reducing bacteria were isolated from the wild plant rhizosphere soils collected at abandoned mine areas, which showed tolerance to high concentration of As(V), in pursuit of potential agents for As(V) bioremediation. METHODS AND RESULTS: Bacterial isolation was performed by a series of enrichment, transfer, and dilutions. Among the isolated strains, two strains (JSAR-1 and JSAR-3) with abilities of tolerance to 10 mM As(V) and Fe(III) reduction were selected. Phylogenetic analysis using 16S rRNA genesequences indicated the closest members of Pseudomonas stutzeri DSM 5190 and Paenibacillus selenii W126, respectively for JSAR-1 and JSAR-3. Ferric and ferrous iron concentrations were measured by ferrozine assay, and arsenic concentration was analyzed by ICP-AES, suggesting inability of As(V) reduction whereas ability of Fe(III) reduction. CONCLUSION: Fe(III)-reducing bacteria isolated from the enrichments with arsenate and ferric iron were found to be resistant to a high concentration of As(III) at 10 mM. We suppose that those kinds of microorganisms may suggest good application potentials for As(V) bioremediation, since the bacteria can transform Fe while surviving under As-contaminated environments. The isolated Fe(III)-reducing bacterial strains could contribute to transformations of iron minerals which may act as effective adsorbents for arsenate, and therefore contribute to As(V) immobilization

Keywords

References

  1. Nickson R, McArthur J, Burgess W, Ahmed KM, Ravenscroft P, Rahman M (1998) Arsenic poisoning of Bangladesh groundwater. Nature, 395: 338. https://doi.org/10.1038/26387.
  2. Oremland RS, Stolz JF (2003) The ecology of arsenic. Science, 300(5621), 939-944. https://doi.org/10.1126/science.1081903.
  3. La Force MJ, Hansel CM, Fendorf S (2000) Arsenic speciation, seasonal transformations, and co-distribution with iron in a mine waste-iInfluenced palustrine emergent wetland. Environmental Science & Technology, 34(18), 3937-3943. https://doi.org/10.1021/es0010150.
  4. Manning BA, Fendorf SE, Goldberg S (1998) Surface structures and stability of arsenic(III) on goethite: Spectroscopic evidence for inner-sphere complexes. Environmental Science & Technology, 32(16), 2383-2388. https://doi.org/10.1021/es9802201.
  5. Shelobolina E, Xu H, Konishi H, Kukkadapu R, Wu T, Blothe M, Roden E (2012) Microbial lithotrophic oxidation of structural Fe(II) in biotite. Applied and Environmental Microbiology, 78(16), 5746-5752. https://doi.org/10.1128/AEM.01034-12.
  6. Fredrickson JK, Zachara JM, Kennedy DW, Dong H, Onstott TC, Hinman NW, Li S-m (1998) Biogenic iron mineralization accompanying the dissimilatory reduction of hydrous ferric oxide by a groundwater bacterium. Geochimica et Cosmochimica Acta, 62(19-20), 3239-3257. https://doi.org/10.1016/S0016-7037(98)00243-9.
  7. Lee JH, Kennedy DW, Dohnalkova A, Moore DA, Nachimuthu P, Reed SB, Fredrickson JK (2011) Manganese sulfide formation via concomitant microbial manganese oxide and thiosulfate reduction. Environmental Microbiology, 13(12), 3275-3288. https://doi.org/10.1111/j.1462-2920.2011.02587.x.
  8. Ludwig W, Strunk O, Westram R, Richter L, Meier H, Yadhukumar, Arno B, Tina L, Susanne S et al. (2004) ARB: a software environment for sequence data. Nucleic Acids Research, 32(4), 1363-1371. https://doi.org/10.1093/nar/gkH293.
  9. Quast C, Pruesse E, Yilmaz P, Gerken J, Schweer T, Yarza P, Jorg P, Frank OG (2013) The SILVA ribosomal RNA gene database project: improved data processing and web-based tools. Nucleic Acids Research, 41(D1), 590-596. https://doi.org/10.1093/nar/gks1219.
  10. Stookey LL (1970) Ferrozine - a new spectrophotometric reagent for iron. Analytical Chemistry, 42(7), 779-781. https://doi.org/10.1021/ac60289a016.
  11. Yalcin S, Le XC (2001) Speciation of arsenic using solid phase extraction cartridges. Journal of Environmental Monitoring, 3(1), 81-85. https://doi.org/10.1039/B007598L.
  12. Jiang S, Lee JH, Kim MG, Myung NV, Fredrickson JK, Sadowsky MJ, Hur HG (2009) Biogenic Formation of As-S Nanotubes by Diverse Shewanella Strains. Applied and Environmental Microbiology, 75(21), 6896-6899. https://doi.org/10.1128/aem.00450-09.