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. 1983 Jun;154(3):1263–1268. doi: 10.1128/jb.154.3.1263-1268.1983

Plasmid-controlled resistance to copper in Escherichia coli.

T J Tetaz, R K Luke
PMCID: PMC217599  PMID: 6343346

Abstract

The copper resistance of a strain of Escherichia coli isolated from the effluent of a piggery where pigs were fed a diet supplemented with copper sulfate was controlled by a conjugative 78-megadalton plasmid designated pRJ1004. Plasmid pRJ1004 exhibited surface exclusion and incompatibility with standard plasmids belonging to incompatibility groups I1 and K. Sensitive strains of E. coli K-12 were unable to form colonies on nutrient agar containing more than 4 mM copper, whereas transconjugants which harbored pRJ1004 were able to form colonies on medium containing up to 20 mM copper.

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Selected References

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

  1. Bachmann B. J., Low K. B. Linkage map of Escherichia coli K-12, edition 6. Microbiol Rev. 1980 Mar;44(1):1–56. doi: 10.1128/mr.44.1.1-56.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bachmann B. J. Pedigrees of some mutant strains of Escherichia coli K-12. Bacteriol Rev. 1972 Dec;36(4):525–557. doi: 10.1128/br.36.4.525-557.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Borck K., Beggs J. D., Brammar W. J., Hopkins A. S., Murray N. E. The construction in vitro of transducing derivatives of phage lambda. Mol Gen Genet. 1976 Jul 23;146(2):199–207. doi: 10.1007/BF00268089. [DOI] [PubMed] [Google Scholar]
  4. Bradley D. E. Morphological and serological relationships of conjugative pili. Plasmid. 1980 Sep;4(2):155–169. doi: 10.1016/0147-619x(80)90005-0. [DOI] [PubMed] [Google Scholar]
  5. Datta N., Hedges R. W. An I pilus-determining R factor with anomalous compatibility properties, mobilizing a gentamicin-resistance plasmid. J Gen Microbiol. 1973 Jul;77(1):11–17. doi: 10.1099/00221287-77-1-11. [DOI] [PubMed] [Google Scholar]
  6. Davey R. B., Pittard J. Endonuclease fingerprinting of plasmids mediating gentamicin resistance in an outbreak of hospital infections. Aust J Exp Biol Med Sci. 1980 Aug;58(4):331–338. doi: 10.1038/icb.1980.32. [DOI] [PubMed] [Google Scholar]
  7. Elek S. D., Higney L. Resistogram typing--a new epidemiological tool: application to Escherichia coli. J Med Microbiol. 1970 Feb;3(1):103–110. doi: 10.1099/00222615-3-1-103. [DOI] [PubMed] [Google Scholar]
  8. Grant A. J., Bird P. I., Pittard J. Naturally occurring plasmids exhibiting incompatibility with members of incompatibility groups I and P. J Bacteriol. 1980 Nov;144(2):758–765. doi: 10.1128/jb.144.2.758-765.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Guerry P., Falkow S., Datta N. R62, a naturally occurring hybrid R plasmid. J Bacteriol. 1974 Jul;119(1):144–151. doi: 10.1128/jb.119.1.144-151.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Ishihara M., Kamio Y., Terawaki Y. Cupric ion resistance as a new genetic marker of a temperature sensitive R plasmid, Rtsl in Escherichia coli. Biochem Biophys Res Commun. 1978 May 15;82(1):74–80. doi: 10.1016/0006-291x(78)90578-8. [DOI] [PubMed] [Google Scholar]
  11. Mandel M., Higa A. Calcium-dependent bacteriophage DNA infection. J Mol Biol. 1970 Oct 14;53(1):159–162. doi: 10.1016/0022-2836(70)90051-3. [DOI] [PubMed] [Google Scholar]
  12. Novick R. P., Clowes R. C., Cohen S. N., Curtiss R., 3rd, Datta N., Falkow S. Uniform nomenclature for bacterial plasmids: a proposal. Bacteriol Rev. 1976 Mar;40(1):168–189. doi: 10.1128/br.40.1.168-189.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Smith H. W. The transfer of antibiotic resistance between strains of enterobacteria in chicken, calves and pigs. J Med Microbiol. 1970 Feb;3(1):165–180. doi: 10.1099/00222615-3-1-165. [DOI] [PubMed] [Google Scholar]
  14. Summers A. O., Jacoby G. A. Plasmid-determined resistance to tellurium compounds. J Bacteriol. 1977 Jan;129(1):276–281. doi: 10.1128/jb.129.1.276-281.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Terawaki Y., Takayasu H., Akiba T. Thermosensitive replication of a kanamycin resistance factor. J Bacteriol. 1967 Sep;94(3):687–690. doi: 10.1128/jb.94.3.687-690.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Varma M. M., Thomas W. A., Prasad C. Resistance to inorganic salts and antibiotics among sewage-borne Enterobacteriaceae and Achromobacteriaceae. J Appl Bacteriol. 1976 Oct;41(2):347–349. doi: 10.1111/j.1365-2672.1976.tb00643.x. [DOI] [PubMed] [Google Scholar]
  17. Wood W. B. Host specificity of DNA produced by Escherichia coli: bacterial mutations affecting the restriction and modification of DNA. J Mol Biol. 1966 Mar;16(1):118–133. doi: 10.1016/s0022-2836(66)80267-x. [DOI] [PubMed] [Google Scholar]

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