Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1989 May;55(5):1196–1202. doi: 10.1128/aem.55.5.1196-1202.1989

Environmental significance of the potential for mer(Tn21)-mediated reduction of Hg2+ to Hg0 in natural waters.

T Barkay 1, C Liebert 1, M Gillman 1
PMCID: PMC184276  PMID: 2547336

Abstract

The role of mer(Tn21) in the adaptation of aquatic microbial communities to Hg2+ was investigated. Elemental mercury was the sole product of Hg2+ volatilization by freshwater and saline water microbial communities. Bacterial activity was responsible for biotransformation because most microeucaryotes did not survive the exposure conditions, and removal of larger microbes (greater than 1 micromole) from adapted communities did not significantly (P greater than 0.01) reduce Hg2+ volatilization rates. DNA sequences homologous to mer(Tn21) were found in 50% of Hg2+-resistant bacterial strains representing two freshwater communities, but in only 12% of strains representing two saline communities (the difference was highly significant; P less than 0.001). Thus, mer(Tn21) played a significant role in Hg2+ resistance among strains isolated from fresh waters, in which microbial activity had a limited role in Hg2+ volatilization. In saline water environments in which microbially mediated volatilization was the major mechanism of Hg2+ loss, other bacterial genes coded for this biotransformation.

Full text

PDF
1196

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Alberts J. J., Schindler J. E., Miller R. W., Nutter D. E., Jr Elemental mercury evolution mediated by humic Acid. Science. 1974 May 24;184(4139):895–897. doi: 10.1126/science.184.4139.895. [DOI] [PubMed] [Google Scholar]
  2. Anast Nick, Smit John. Isolation and Characterization of Marine Caulobacters and Assessment of Their Potential for Genetic Experimentation. Appl Environ Microbiol. 1988 Mar;54(3):809–817. doi: 10.1128/aem.54.3.809-817.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Babich H., Stotzky G. Differential toxicities of mercury to bacteria and bacteriophages in sea and in lake water. Can J Microbiol. 1979 Nov;25(11):1252–1257. doi: 10.1139/m79-197. [DOI] [PubMed] [Google Scholar]
  4. Barkay T. Adaptation of aquatic microbial communities to hg stress. Appl Environ Microbiol. 1987 Dec;53(12):2725–2732. doi: 10.1128/aem.53.12.2725-2732.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Barkay T., Fouts D. L., Olson B. H. Preparation of a DNA gene probe for detection of mercury resistance genes in gram-negative bacterial communities. Appl Environ Microbiol. 1985 Mar;49(3):686–692. doi: 10.1128/aem.49.3.686-692.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Barkay T., Pritchard H. Adaptation of aquatic microbial communities to pollutant stress. Microbiol Sci. 1988 Jun;5(6):165–169. [PubMed] [Google Scholar]
  7. Caron D. A. Technique for enumeration of heterotrophic and phototrophic nanoplankton, using epifluorescence microscopy, and comparison with other procedures. Appl Environ Microbiol. 1983 Aug;46(2):491–498. doi: 10.1128/aem.46.2.491-498.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Compeau G. C., Bartha R. Effect of salinity on mercury-methylating activity of sulfate-reducing bacteria in estuarine sediments. Appl Environ Microbiol. 1987 Feb;53(2):261–265. doi: 10.1128/aem.53.2.261-265.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Compeau G. C., Bartha R. Sulfate-reducing bacteria: principal methylators of mercury in anoxic estuarine sediment. Appl Environ Microbiol. 1985 Aug;50(2):498–502. doi: 10.1128/aem.50.2.498-502.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Compeau G., Bartha R. Methylation and demethylation of mercury under controlled redox, pH and salinity conditions. Appl Environ Microbiol. 1984 Dec;48(6):1203–1207. doi: 10.1128/aem.48.6.1203-1207.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Cripe C. R., Walker W. W., Pritchard P. H., Bourquin A. W. A shake-flask test for estimation of biodegradability of toxic organic substances in the aquatic environment. Ecotoxicol Environ Saf. 1987 Dec;14(3):239–251. doi: 10.1016/0147-6513(87)90067-4. [DOI] [PubMed] [Google Scholar]
  12. Furutani A., Rudd J. W. Measurement of mercury methylation in lake water and sediment samples. Appl Environ Microbiol. 1980 Oct;40(4):770–776. doi: 10.1128/aem.40.4.770-776.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hobbie J. E., Daley R. J., Jasper S. Use of nuclepore filters for counting bacteria by fluorescence microscopy. Appl Environ Microbiol. 1977 May;33(5):1225–1228. doi: 10.1128/aem.33.5.1225-1228.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Jain R. K., Burlage R. S., Sayler G. S. Methods for detecting recombinant DNA in the environment. Crit Rev Biotechnol. 1988;8(1):33–84. doi: 10.3109/07388558809150537. [DOI] [PubMed] [Google Scholar]
  15. Ji G. Y., Salzberg S. P., Silver S. Cell-free mercury volatilization activity from three marine caulobacter strains. Appl Environ Microbiol. 1989 Feb;55(2):523–525. doi: 10.1128/aem.55.2.523-525.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Kellogg S. T., Chatterjee D. K., Chakrabarty A. M. Plasmid-assisted molecular breeding: new technique for enhanced biodegradation of persistent toxic chemicals. Science. 1981 Dec 4;214(4525):1133–1135. doi: 10.1126/science.7302584. [DOI] [PubMed] [Google Scholar]
  17. Le Rudulier D., Strom A. R., Dandekar A. M., Smith L. T., Valentine R. C. Molecular biology of osmoregulation. Science. 1984 Jun 8;224(4653):1064–1068. doi: 10.1126/science.224.4653.1064. [DOI] [PubMed] [Google Scholar]
  18. Silver S., Misra T. K. Plasmid-mediated heavy metal resistances. Annu Rev Microbiol. 1988;42:717–743. doi: 10.1146/annurev.mi.42.100188.003441. [DOI] [PubMed] [Google Scholar]
  19. Spain J. C., Pritchard P. H., Bourquin A. W. Effects of adaptation on biodegradation rates in sediment/water cores from estuarine and freshwater environments. Appl Environ Microbiol. 1980 Oct;40(4):726–734. doi: 10.1128/aem.40.4.726-734.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Spain J. C., Van Veld P. A., Monti C. A., Pritchard P. H., Cripe C. R. Comparison of p-Nitrophenol Biodegradation in Field and Laboratory Test Systems. Appl Environ Microbiol. 1984 Nov;48(5):944–950. doi: 10.1128/aem.48.5.944-950.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Steffan R. J., Korthals E. T., Winfrey M. R. Effects of acidification on mercury methylation, demethylation, and volatilization in sediments from an acid-susceptible lake. Appl Environ Microbiol. 1988 Aug;54(8):2003–2009. doi: 10.1128/aem.54.8.2003-2009.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Summers A. O. Organization, expression, and evolution of genes for mercury resistance. Annu Rev Microbiol. 1986;40:607–634. doi: 10.1146/annurev.mi.40.100186.003135. [DOI] [PubMed] [Google Scholar]
  23. Summers A. O., Silver S. Mercury resistance in a plasmid-bearing strain of Escherichia coli. J Bacteriol. 1972 Dec;112(3):1228–1236. doi: 10.1128/jb.112.3.1228-1236.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Summers A. O., Silver S. Microbial transformations of metals. Annu Rev Microbiol. 1978;32:637–672. doi: 10.1146/annurev.mi.32.100178.003225. [DOI] [PubMed] [Google Scholar]
  25. Weiss A. A., Murphy S. D., Silver S. Mercury and organomercurial resistances determined by plasmids in Staphylococcus aureus. J Bacteriol. 1977 Oct;132(1):197–208. doi: 10.1128/jb.132.1.197-208.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Wyndham R. C. Evolved aniline catabolism in Acinetobacter calcoaceticus during continuous culture of river water. Appl Environ Microbiol. 1986 Apr;51(4):781–789. doi: 10.1128/aem.51.4.781-789.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES