Abstract
The effects of sodium ions on the uptake of Hg2+ and induction of the Tn21 mer operon were studied by using Escherichia coli HMS174 harboring the reporter plasmids pRB28 and pOS14. Plasmid pRB28 carries merRT', and pOS14 carries merRTPC of the mer operon, both cloned upstream of a promoterless luciferase gene cassette in pUCD615. The bioluminescent response to 1 microM Hg2+ was significantly inhibited in E. coli HMS174(pRB28) in minimal medium supplemented with sodium ions at 10 to 140 mM. After initial acceleration, light emission declined at 50 nM Hg2+ in the presence of Na+. The mer-lux assay with resting cells carrying pRB28 and 203Hg2+ uptake experiments showed increased induction and enhanced mercury uptake, respectively, in media supplemented with sodium ions. The presence of Na+ facilitated maintenance of bioluminescence in resting HMS174(pRB28) cells induced with 50 nM Hg2+. External K+ stimulated bioluminescent response in HMS174(pRB28) and HMS174(pOS14) grown in sodium phosphate minimal medium devoid of potassium ions. Sodium ions appear to facilitate mercury transport. We propose that sodium-coupled transport of mercuric ions can be one of the mechanisms for mercury uptake by E. coli and that the Na+ gradient may energize the transport of Hg2+.
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Selected References
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- Bogdanova E. S., Mindlin S. Z., Pakrová E., Kocur M., Rouch D. A. Mercuric reductase in environmental gram-positive bacteria sensitive to mercury. FEMS Microbiol Lett. 1992 Oct 1;76(1-2):95–100. doi: 10.1016/0378-1097(92)90370-4. [DOI] [PubMed] [Google Scholar]
- Brown N. L., Camakaris J., Lee B. T., Williams T., Morby A. P., Parkhill J., Rouch D. A. Bacterial resistances to mercury and copper. J Cell Biochem. 1991 Jun;46(2):106–114. doi: 10.1002/jcb.240460204. [DOI] [PubMed] [Google Scholar]
- Cairney J., Higgins C. F., Booth I. R. Proline uptake through the major transport system of Salmonella typhimurium is coupled to sodium ions. J Bacteriol. 1984 Oct;160(1):22–27. doi: 10.1128/jb.160.1.22-27.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Campbell J. L., Richardson C. C., Studier F. W. Genetic recombination and complementation between bacteriophage T7 and cloned fragments of T7 DNA. Proc Natl Acad Sci U S A. 1978 May;75(5):2276–2280. doi: 10.1073/pnas.75.5.2276. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Condee C. W., Summers A. O. A mer-lux transcriptional fusion for real-time examination of in vivo gene expression kinetics and promoter response to altered superhelicity. J Bacteriol. 1992 Dec;174(24):8094–8101. doi: 10.1128/jb.174.24.8094-8101.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dimroth P. A new sodium-transport system energized by the decarboxylation of oxaloacetate. FEBS Lett. 1980 Dec 29;122(2):234–236. doi: 10.1016/0014-5793(80)80446-7. [DOI] [PubMed] [Google Scholar]
- Dimroth P. Sodium ion transport decarboxylases and other aspects of sodium ion cycling in bacteria. Microbiol Rev. 1987 Sep;51(3):320–340. doi: 10.1128/mr.51.3.320-340.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Foster T. J., Nakahara H., Weiss A. A., Silver S. Transposon A-generated mutations in the mercuric resistance genes of plasmid R100-1. J Bacteriol. 1979 Oct;140(1):167–181. doi: 10.1128/jb.140.1.167-181.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hamlett N. V., Landale E. C., Davis B. H., Summers A. O. Roles of the Tn21 merT, merP, and merC gene products in mercury resistance and mercury binding. J Bacteriol. 1992 Oct;174(20):6377–6385. doi: 10.1128/jb.174.20.6377-6385.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heefner D. L., Harold F. M. ATP-driven sodium pump in Streptococcus faecalis. Proc Natl Acad Sci U S A. 1982 May;79(9):2798–2802. doi: 10.1073/pnas.79.9.2798. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heitzer A., Webb O. F., Thonnard J. E., Sayler G. S. Specific and quantitative assessment of naphthalene and salicylate bioavailability by using a bioluminescent catabolic reporter bacterium. Appl Environ Microbiol. 1992 Jun;58(6):1839–1846. doi: 10.1128/aem.58.6.1839-1846.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Krulwich T. A. Na+/H+ antiporters. Biochim Biophys Acta. 1983 Dec 30;726(4):245–264. doi: 10.1016/0304-4173(83)90011-3. [DOI] [PubMed] [Google Scholar]
- Kusano T., Ji G. Y., Inoue C., Silver S. Constitutive synthesis of a transport function encoded by the Thiobacillus ferrooxidans merC gene cloned in Escherichia coli. J Bacteriol. 1990 May;172(5):2688–2692. doi: 10.1128/jb.172.5.2688-2692.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lanyi J. K. The role of Na+ in transport processes of bacterial membranes. Biochim Biophys Acta. 1979 Dec 20;559(4):377–397. doi: 10.1016/0304-4157(79)90011-x. [DOI] [PubMed] [Google Scholar]
- Lund P. A., Brown N. L. Role of the merT and merP gene products of transposon Tn501 in the induction and expression of resistance to mercuric ions. Gene. 1987;52(2-3):207–214. doi: 10.1016/0378-1119(87)90047-3. [DOI] [PubMed] [Google Scholar]
- MITCHELL P. Coupling of phosphorylation to electron and hydrogen transfer by a chemi-osmotic type of mechanism. Nature. 1961 Jul 8;191:144–148. doi: 10.1038/191144a0. [DOI] [PubMed] [Google Scholar]
- Meighen E. A. Molecular biology of bacterial bioluminescence. Microbiol Rev. 1991 Mar;55(1):123–142. doi: 10.1128/mr.55.1.123-142.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Misra T. K. Bacterial resistances to inorganic mercury salts and organomercurials. Plasmid. 1992 Jan;27(1):4–16. doi: 10.1016/0147-619x(92)90002-r. [DOI] [PubMed] [Google Scholar]
- Mitchell P. Performance and conservation of osmotic work by proton-coupled solute porter systems. J Bioenerg. 1973 Jan;4(1):63–91. doi: 10.1007/BF01516051. [DOI] [PubMed] [Google Scholar]
- Nakahara H., Silver S., Miki T., Rownd R. H. Hypersensitivity to Hg2+ and hyperbinding activity associated with cloned fragments of the mercurial resistance operon of plasmid NR1. J Bacteriol. 1979 Oct;140(1):161–166. doi: 10.1128/jb.140.1.161-166.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- O'Halloran T. V., Frantz B., Shin M. K., Ralston D. M., Wright J. G. The MerR heavy metal receptor mediates positive activation in a topologically novel transcription complex. Cell. 1989 Jan 13;56(1):119–129. doi: 10.1016/0092-8674(89)90990-2. [DOI] [PubMed] [Google Scholar]
- Ralston D. M., O'Halloran T. V. Ultrasensitivity and heavy-metal selectivity of the allosterically modulated MerR transcription complex. Proc Natl Acad Sci U S A. 1990 May;87(10):3846–3850. doi: 10.1073/pnas.87.10.3846. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sahlman L., Jonsson B. H. Purification and properties of the mercuric-ion-binding protein MerP. Eur J Biochem. 1992 Apr 1;205(1):375–381. doi: 10.1111/j.1432-1033.1992.tb16790.x. [DOI] [PubMed] [Google Scholar]
- Scott D. M. Sodium cotransport systems: cellular, molecular and regulatory aspects. Bioessays. 1987 Aug;7(2):71–78. doi: 10.1002/bies.950070206. [DOI] [PubMed] [Google Scholar]
- Selifonova O., Burlage R., Barkay T. Bioluminescent sensors for detection of bioavailable Hg(II) in the environment. Appl Environ Microbiol. 1993 Sep;59(9):3083–3090. doi: 10.1128/aem.59.9.3083-3090.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Silver S., Walderhaug M. Gene regulation of plasmid- and chromosome-determined inorganic ion transport in bacteria. Microbiol Rev. 1992 Mar;56(1):195–228. doi: 10.1128/mr.56.1.195-228.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Skulachev V. P. Membrane-linked energy transductions. Bioenergetic functions of sodium: H+ is not unique as a coupling ion. Eur J Biochem. 1985 Sep 2;151(2):199–208. doi: 10.1111/j.1432-1033.1985.tb09088.x. [DOI] [PubMed] [Google Scholar]
- Stewart G. S. In vivo bioluminescence: new potentials for microbiology. Lett Appl Microbiol. 1990 Jan;10(1):1–8. doi: 10.1111/j.1472-765x.1990.tb00082.x. [DOI] [PubMed] [Google Scholar]
- Summers A. O., Kight-Olliff L. Tn1 generated mutants in the mercuric ion reductase of the Inc P plasmid, R702. Mol Gen Genet. 1980;180(1):91–97. doi: 10.1007/BF00267356. [DOI] [PubMed] [Google Scholar]
- 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]
- Tokuda H., Unemoto T. Characterization of the respiration-dependent Na+ pump in the marine bacterium Vibrio alginolyticus. J Biol Chem. 1982 Sep 10;257(17):10007–10014. [PubMed] [Google Scholar]