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. 1981 Sep;147(3):1110–1112. doi: 10.1128/jb.147.3.1110-1112.1981

Translocatable resistance to mercuric and phenylmercuric ions in soil bacteria.

A J Radford, J Oliver, W J Kelly, D C Reanney
PMCID: PMC216152  PMID: 6268601

Abstract

Of a sample of 42 gram-negative Hg-resistant bacteria, three (a Pseudomonas fluorescens, a Klebsiella sp. and a Citrobacter sp.) contained translocatable elements conferring resistance to Hg2+ (all three) and to Hg2+ and phenylmercuric acetate (P. fluorescens). The discovery of transposable phenylmercuric acetate resistance extends the range of known resistance "transposons" from heavy metals and antibiotics to organometallic compounds.

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Selected References

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  1. Courvalin P., Weisblum B., Davies J. Aminoglycoside-modifying enzyme of an antibiotic-producing bacterium acts as a determinant of antibiotic resistance in Escherichia coli. Proc Natl Acad Sci U S A. 1977 Mar;74(3):999–1003. doi: 10.1073/pnas.74.3.999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Humphreys G. O., Willshaw G. A., Anderson E. S. A simple method for the preparation of large quantities of pure plasmid DNA. Biochim Biophys Acta. 1975 Apr 2;383(4):457–463. doi: 10.1016/0005-2787(75)90318-4. [DOI] [PubMed] [Google Scholar]
  3. Nakahara H., Ishikawa T., Sarai Y., Kondo I. Frequency of heavy-metal resistance in bacteria from inpatients in Japan. Nature. 1977 Mar 10;266(5598):165–167. doi: 10.1038/266165a0. [DOI] [PubMed] [Google Scholar]
  4. Nakahara H., Ishikawa T., Sarai Y., Kondo I., Kozukue H. Mercury resistance and R plasmids in Escherichia coli isolated from clinical lesions in Japan. Antimicrob Agents Chemother. 1977 Jun;11(6):999–1003. doi: 10.1128/aac.11.6.999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Nakahara H., Ishikawa T., Sarai Y., Kondo I., Kozukue H., Silver S. Linkage of mercury, cadmium, and arsenate and drug resistance in clinical isolates of Pseudomonas aeruginosa. Appl Environ Microbiol. 1977 Apr;33(4):975–976. doi: 10.1128/aem.33.4.975-976.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Olsen R. H., Shipley P. L. RP1 properties and fertility inhibition among P, N, W, and X incompatibility group plasmids. J Bacteriol. 1975 Jul;123(1):28–35. doi: 10.1128/jb.123.1.28-35.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Olsen R. H., Shipley P. Host range and properties of the Pseudomonas aeruginosa R factor R1822. J Bacteriol. 1973 Feb;113(2):772–780. doi: 10.1128/jb.113.2.772-780.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Olsen R. H., Thomas D. D. Characteristics and purification of PRR1, an RNA phage specific for the broad host range Pseudomonas R1822 drug resistance plasmid. J Virol. 1973 Dec;12(6):1560–1567. doi: 10.1128/jvi.12.6.1560-1567.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Schottel J., Mandal A., Clark D., Silver S., Hedges R. W. Volatilisation of mercury and organomercurials determined by inducible R-factor systems in enteric bacteria. Nature. 1974 Sep 27;251(5473):335–337. doi: 10.1038/251335a0. [DOI] [PubMed] [Google Scholar]
  10. Stanisich V. A., Bennett P. M., Richmond M. H. Characterization of a translocation unit encoding resistance to mercuric ions that occurs on a nonconjugative plasmid in Pseudomonas aeruginosa. J Bacteriol. 1977 Mar;129(3):1227–1233. doi: 10.1128/jb.129.3.1227-1233.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Summers A. O., Weiss R. B., Jacoby G. A. Transposition of mercury resistance from a transferable R plasmic of Escherichia coli. Plasmid. 1980 Jan;3(1):35–47. doi: 10.1016/s0147-619x(80)90032-3. [DOI] [PubMed] [Google Scholar]

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