Identification and characterization of metabolic properties of bacterial populations recovered fromarsenic contaminated ground water ofNorthEast India (Assam)

Water Research

Volumn 47, Issue 19, 2013, Pages 6992-7005

  Ghosh, Soma ^a   Sar, Pinaki ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY   (India)

Author keywords

Acidovorax; Acinetobacter; Arsenic contamination; Assam; Biogeochemical cycling; Brevundimonas; Groundwater

Indexed keywords

BACTERIA; BACTERIOLOGY; CONTAMINATION; GENES; GROUNDWATER; GROUNDWATER POLLUTION; IRON COMPOUNDS; METABOLISM; RNA;

ACIDOVORAX; ACINETOBACTERS; ARSENIC CONTAMINATION; ASSAM; BIOGEOCHEMICAL CYCLING; BREVUNDIMONAS;

SELENIUM COMPOUNDS;

ARSENIC; GROUND WATER; OXIDOREDUCTASE; RNA 16S; SIDEROPHORE;

ARSENIC; BACTERIUM; BIOGEOCHEMICAL CYCLE; ENRICHMENT; ENZYME ACTIVITY; GENETIC ANALYSIS; GROUNDWATER POLLUTION; METABOLISM; MICROBIAL COMMUNITY; MOBILIZATION; RELATIVE ABUNDANCE; SIDEROPHORE; SPECIES DIVERSITY;

ACIDOVORAX; ACINETOBACTER; ANAEROBIC METABOLISM; ARTICLE; BACILLUS; BACTERIAL STRAIN; BACTERIUM; BREVUNDIMONAS; CARBON SOURCE; CAULOBACTER; CONTROLLED STUDY; ELECTRON; ENZYME ACTIVITY; GENE SEQUENCE; HERBASPIRILLUM; INDIA; METABOLISM; NONHUMAN; PRIORITY JOURNAL; PSEUDOMONAS; RALSTONIA; RHIZOBIALES; RHODOCOCCUS; STAPHYLOCOCCUS; WATER CONTAMINATION;

ASSAM; INDIA;

ACIDOVORAX; ACINETOBACTER; BACILLUS (BACTERIUM); BACTERIA (MICROORGANISMS); BOSEA (BACTERIA); BREVUNDIMONAS; CAULOBACTER; HERBASPIRILLUM; PSEUDOMONAS; RALSTONIA; RHIZOBIALES; RHODOCOCCUS; STAPHYLOCOCCUS;

ACIDOVORAX; ACINETOBACTER; ARSENIC CONTAMINATION; ASSAM; BIOGEOCHEMICAL CYCLING; BREVUNDIMONAS; GROUNDWATER;

ARSENIC; BACTERIA; CAULOBACTERACEAE; COMAMONADACEAE; CYTOSOL; GROUNDWATER; INDIA; MOLECULAR SEQUENCE DATA; RNA, RIBOSOMAL, 16S; WATER POLLUTANTS, CHEMICAL;

EID: 84888129241     PISSN: 00431354     EISSN: 18792448     Source Type: Journal    
DOI: 10.1016/j.watres.2013.08.044     Document Type: Article

References (51)

1. Achour-Rokbani A., Bauda P., Billard P. Diversity of As(III) transporter genes from As-resistant soil bacteria. Res. Microbiol. 2007, 158:128-137.
2. Battaglia-Brunet F., Dictor M.C., Garrido F., Crouzet C., Morin D., Dekeyser K., Clarens M., Baranger P. An As(III)-oxidizing bacterial population: selection, characterization and performance in reactors. J. Appl. Microbiol. 2002, 93:656-667.
3. Cai L., Liu G., Rensing C., Wang G. Genes involved in As transformation and resistance associated with different levels of As-contaminated soils. BMC Microbiol. 2009, 9:4.
4. Cavalca L., Zanchi R., Corsini A., Colombo M., Romagnoli C., Canzi E., Andreoni V. As-resistant bacteria associated with roots of the wild Cirsium arvense (L) plant from an As polluted soil, and screening of potential plant growth-promoting characteristics. Syst. Appl. Microbiol. 2010, 33:154-164.
5. Chatterjee A., Das D., Chakraborti D. A study of ground water contamination by As in the residential area of Behala, Calcutta due to industrial pollution. Environ. Pollut. 1993, 80:57-65.
6. Chen Y., Wu L., Boden R., Hillebrand A., Kumaresan D., Moussard H., Baciu M., Lu Y., Murrell C. Life without light: microbial diversity and evidence of sulfur- and ammonium-based chemolithotrophy in Movile Cave. ISME J. 2009, 3:1093-1104.
7. Davolos D., Pietrangeli B. A molecular study on bacterial resistance to arsenic-toxicity in surface and underground waters of Latium. Ecotoxicol. Environ. Saf. 2013, 96:1-9.
8. Drewniak L., Styczek A., Lopatka M.M., Sklodowska A. Bacteria, hypertolerant to As in the rocks of an ancient gold mine, and their potential role in dissemination of As pollution. Environ. Pollut. 2008, 156:1069-1074.
9. Enmark G., Nordborg D. Arsenic in the Groundwater of the Brahmaputra Floodplains, Assam, India - Source, Distribution and Release Mechanisms 2007, Arbetsgruppen för Tropisk Ekologi Minor Field Study 131 Committee of Tropical Ecology, Uppsala University, Sweden.
10. Fan H., Su C., Wang Y., Yao J., Zhao K., Wang Y., Wang G. Sedimentary arsenite-oxidizing and arsenate-reducing bacteria associated with high arsenic groundwater from Shanyin, Northwestern China. J. Appl. Microbiol. 2008, 105:529-539.
11. Fendorf S., Michael H.A., Van Geen A. Spatial and temporal variations of groundwater As in south and south east Asia. Science 2010, 328:1123-1127.
12. Gault A.G., Cooke D.R., Townsend A.T., Charnock J.M., Polya D.A. Mechanisms of arsenic attenuation in acid mine drainage from Mount Bischoff, western Tasmania. Sci. Total Environ. 2005, 345:219-228.
13. Gihring T.M., Druschel G.K., McCleskey R.B., Hamers R.J., Banfield J.F. Rapid As(III)oxidation by Thermus aquaticus and Thermus thermophilus: field and laboratory investigations. Environ. Sci. Technol. 2001, 35:3857-3862.
14. Gorra R., Webster G., Martin M., Celi L., Mapelli F., Weightman A.J. Dynamic microbial community associated with iron-arsenic co-precipitation products from a groundwater storage system in Bangladesh. Microb. Ecol. 2012, 64,171-64,186.
15. Hery M., Van Dongen B.E., Gill F., Mondal D., Vaughan D.J., Pancost R.D., Polya D.A., Lloyd J.R. As release and attenuation in low organic carbon aquifer sediments from West Bengal. Geobiology 2010, 8:155-168.
16. Huang Y., Li H., Rensing C., Zhao K., Johnstone L., Wang G. Genome sequence of the facultative anaerobic arsenite-oxidizing and nitrate-reducing bacterium Acidovorax sp. strain NO1. J. Bacteriol. 2012, 194:1635-1636.
17. Ilyaletdinov A.N., Abdrashitova S.A. Autotrophic oxidation of arsenic by a culture of Pseudomonas arsenitoxidans. Mikrobiologiya 1981, 50:197-204.
18. Islam E., Sar P. Culture-dependent and -independent molecular analysis of bacterial community within uranium ore. J. Basic Microbiol. 2011, 1-13.
19. Islam F.S., Boothman C., Gault A.G., Polya D.A., Lloyd J.R. Potential role of the Fe(III)-reducing bacteria Geobacter and Geothrix in controlling arsenic solubility in Bengal delta sediments. Mineral. Mag. 2005, 69:865-875.
20. Islam F.S., Gault A.G., Boothman C., Polya D.A., Charnock J.M., Chatterjee D., Lloyd J.R. Role of metal-reducing bacteria in As release from Bengal delta sediments. Nature 2004, 430:68-71.
21. Jackson C.R., Jackson E.F., Dugas S.L., Gamble K., Williams S.E. Microbial transformations of As(III)and As(V) in natural environments. Recent Res. Dev. Microbiol. 2003, 7:103-118.
22. Kar S., Maitya J.P., Jeana J., Liua C.,C., Nath B., Yanga H.J., Bundschuha J. Arsenic-enriched aquifers: occurrences and mobilization of arsenic in groundwater of Ganges Delta Plain, Barasat, West Bengal, India. Appl. Geochem. 2010, 25:1805-1814.
23. Kazy S.K., Sar P., Asthana R.K., Singh S.P. Copper uptake and its compartmentalization in Pseudomonas aeruginosa strains: chemical nature of cellular metal. World J. Microbiol. Biotechnol. 1999, 15:599-605.
24. Laverman A.M., Blum S.J., Schaefer J.K., Philips E.J.P., Lovley D.R., Oremland R.S. Growth of strain SES-3 with As(V) and other diverse electron acceptors. Appl. Environ. Microbiol. 1995, 61:3556-3561.
25. Luli G.W., Talnagi J.W., Strohl W.R., Pfister R.M. Hexavalent chromium resistant bacteria isolated from river sediments. Appl. Environ. Microbiol. 1983, 46:846-854.
26. Li D., Li Z., Yu J., Cao N., Liu R., Yang M. Characterization of bacterial community structure in a drinking water distribution system during an occurrence of red water. Appl. Environ. Microbiol. 2010, 76:7171-7180.
27. Liao V.H.C., Chu Y.J., Su Y.C., Hsiao S.Y., Wei C.C., Liu C.W., Liao C.M., Shen W.C., Chang F.J. Arsenite-oxidizing and As(V)reducing bacteria associated with As-rich groundwater in Taiwan. J. Contam. Hydrol. 2011, 123:20-29.
28. Macur R.E., Jackson C.R., Botero L.M., Mcdermott T.R., Inskeep W.P. Bacterial populations associated with the oxidation and reduction of As in an unsaturated soil. Environ. Sci. Technol. 2004, 38:104-111.
29. Mailloux B.J., Alexandrova E., Alison R. Microbial mineral weathering for nutrient acquisition releases As. Appl. Environ. Microbiol. 2009, 75:2558-2565.
30. Matthijs S., Laus G., Meyer J.M., Abbaspour-Tehrani K., Schafer M., Budzikiewicz H., Cornelis P. Siderophore-mediated iron acquisition in the entomopathogenic bacterium Pseudomonas entomophila L48 and its close relative Pseudomonas putida KT2440. Biometals 2009, 22(6):951-964.
31. Muyzer G., de Waal E.C., Uitterlinden A.G. Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes coding for 16S rRNA. Appl. Environ. Microbiol. 1993, 59:695-700.
32. Nair A., Juwarkar A.A., Singh S.K. Production and characterization of siderophores and its application in As removal from contaminated soil. Water Air Soil Pollut. 2007, 180:199-212.
33. Nazina T.N., Kosareva I.M., Davydov A.S., Turova T.P., Novikova E.V., Khafizov R.R., Poltaraus A.B. Physico-chemical and microbiological characteristics of groundwater from observation boreholes of a deep radioactive liquid waste repository. Mikrobiologiia 2000, 105-112.
34. Nickson R.T., McArthur J.M., Ravenscroft P., Burgess W.G., Ahmed K.M. Mechanism of arsenic release to groundwater, Bangladesh and West Bengal. Appl. Geochem. 2000, 15:403-413.
35. Oremland R.S., Kulp T.R., Switzer B.J., Hoeft S.E., Baesman S., Miller G., Stolz J.,F. A microbial As cycle in a salt saturated, extreme environment. Science 2005, 308:1305-1308.
36. Oremland R.S., Hoeft S.E., Santini J.M., Bano N., Hollibaugh R.A., Hollibaugh J.T. Anaerobic oxidation of arsenite in mono lake water and by a facultative arsenite-oxidizing chemoautotroph, strain MLHE-1. Appl. Environ. Microbiol. 2002, 68:4795-4802.
37. Oremland R.S., Stolz J.F. The ecology of As. Science 2003, 300:939-944.
38. Reasoner D.J., Geldreich E.E. A new medium for the enumeration and subculture of bacteria from potable water. Appl. Environ. Microbiol. 1985, 49:1-7.
39. Santini J.M., Sly L.I., Schnagl R.D., Macy J.M. A new chemolithoautotrophic arsenite-oxidizing bacterium isolated from a gold mine: phylogenetic, physiological, and preliminary biochemical studies. Appl. Environ. Microbiol. 2000, 66:92-97.
40. Sarkar A., Kazy S.K., Sar P. Characterization of As resistant bacteria from As rich groundwater of West Bengal. Ecotoxicology 2013, 22:363-374.
41. Shimizu S., Akiyama M., Ishijima Y., Hama K., Kunimaru T., Naganuma T. Molecular characterization of microbial communities in fault-bordered aquifers in the Miocene formation of northernmost Japan. Geobiology 2006, 4:147-223.
42. Silver S., Phung L.T. Genes and enzymes involved in bacterial oxidation and reduction of inorganic As. Appl. Environ. Microbiol. 2005, 71:599-608.
43. Singh A.K. Chemistry of As in ground water of Ganges-Brahmputra river basin, India. Curr. Sci. 2006, 91:1-7.
44. Slyemi D., Bonnefoy V. How prokaryotes deal with As. Environ. Microbiol. Rep. 2011, 1:16.
45. Sriyosachati S., Cox C.D. Siderophore-mediated iron acquisition from transferrin by Pseudomonas aeruginosa. Infect. Immun. 1986, 52:885-891.
46. Sultana M., Hartig C., Planer-Friedrich B., Seifert J., Schlomann M. Bacterial communities in Bangladesh aquifers differing in aqueous As concentration. Geomicrobiol. J. 2011, 28:198-211.
47. Sutton N.B., van der Kraan G.M., van Loosdrecht M.C., Muyzer G., Bruining J., Schotting R.J. Characterization of geochemical constituents and bacterial populations associated with As mobilization in deep and shallow tube wells in Bangladesh. Water Res. 2009, 43:1720-1730.
48. Tamura K., Dudley J., Nei M., Kumar S. MEGA4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol. Biol. Evol. 2007, 24:1596-1599.
49. Tiago I., Chung A.P., Verissimo A. Bacterial diversity in a nonsaline alkaline environment: heterotrophic aerobic populations. Appl. Environ. Microbiol. 2004, 70(12):7378-7387.
50. Vala A.K., Dave B.P., Dube H.C. Chemical characterization and quantification of siderophores produced by marine and terrestrial aspergilli. Can. J. Microbiol. 2006, 52:603-607.
51. Zhao Z., Jiaa Y., Xua L., Zhaoc S. Adsorption and heterogeneous oxidation of As(III) on ferrihydrite. Water Res. 2011, 45:6496-6504.