Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1973 Sep;115(3):1130–1134. doi: 10.1128/jb.115.3.1130-1134.1973

Deoxyribonucleic Acid-Deoxyribonucleic Acid Hybridization of R Factors

Lewis C Ingram 1
PMCID: PMC246362  PMID: 4199506

Abstract

A new method of estimating deoxyribonucleic acid homology is presented and used to measure the homology between bacterial plasmids of different compatibility groups. Deoxyribonucleic acid of the P-group plasmid RP1, originally isolated in Pseudomonas aeruginosa, has considerable (50%) homology with an N-group plasmid of the Enterobacteriaceae.

Full text

PDF
1130

Selected References

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

  1. Cohen S. N., Miller C. A. Non-chromosomal antibiotic resistance in bacteria. II. Molecular nature of R-factors isolated from Proteus mirabilis and Escherichia coli. J Mol Biol. 1970 Jun 28;50(3):671–687. doi: 10.1016/0022-2836(70)90092-6. [DOI] [PubMed] [Google Scholar]
  2. Datta N., Hedges R. W. Compatibility groups among fi - R factors. Nature. 1971 Nov 26;234(5326):222–223. doi: 10.1038/234222a0. [DOI] [PubMed] [Google Scholar]
  3. Datta N., Hedges R. W. R factors identified in Paris, some conferring gentamicin resistance, constitute a new compatibility group. Ann Inst Pasteur (Paris) 1972 Dec;123(6):849–852. [PubMed] [Google Scholar]
  4. Denhardt D. T. A membrane-filter technique for the detection of complementary DNA. Biochem Biophys Res Commun. 1966 Jun 13;23(5):641–646. doi: 10.1016/0006-291x(66)90447-5. [DOI] [PubMed] [Google Scholar]
  5. Grinsted J., Saunders J. R., Ingram L. C., Sykes R. B., Richmond M. H. Properties of a R factor which originated in Pseudomonas aeruginosa 1822. J Bacteriol. 1972 May;110(2):529–537. doi: 10.1128/jb.110.2.529-537.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Guerry P., Falkow S. Polynucleotide sequence relationships among some bacterial plasmids. J Bacteriol. 1971 Jul;107(1):372–374. doi: 10.1128/jb.107.1.372-374.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Ingram L. C., Richmond M. H., Sykes R. B. Molecular characterization of the R factors implicated in the carbenicillin resistance of a sequence of Pseudomonas aeruginosa strains isolated from burns. Antimicrob Agents Chemother. 1973 Feb;3(2):279–288. doi: 10.1128/aac.3.2.279. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Ingram L., Sykes R. B., Grinsted J., Saunders J. R., Richmond M. H. A transmissible resistance element from a strain of Pseudomonas aeruginosa containing no detectable extrachromosomal DNA. J Gen Microbiol. 1972 Sep;72(2):269–279. doi: 10.1099/00221287-72-2-269. [DOI] [PubMed] [Google Scholar]
  9. Kontomichalou P., Mitani M., Clowes R. C. Circular R-factor molecules controlling penicillinase synthesis, replicating in Escherichia coli under either relaxed or stringent control. J Bacteriol. 1970 Oct;104(1):34–44. doi: 10.1128/jb.104.1.34-44.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Lawn A. M., Meynell G. G., Meynell E., Datta N. Sex pili and the classification of sex factors in the enterobacteriaceae. Nature. 1967 Oct 28;216(5113):343–346. doi: 10.1038/216343a0. [DOI] [PubMed] [Google Scholar]
  11. Watanabe T., Ogata C. Episome-mediated transfer of drug resistance in Enterobacteriaceae. IX. Recombination of an R factor with F. J Bacteriol. 1966 Jan;91(1):43–50. doi: 10.1128/jb.91.1.43-50.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES