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. 1973 Apr;114(1):424–433. doi: 10.1128/jb.114.1.424-433.1973

Detection and Characterization of Plasmids in Pseudomonas aeruginosa Strain PAO

J M Pemberton 1, Alvin J Clark 1
PMCID: PMC251781  PMID: 4633347

Abstract

Using a variety of techniques, it has been established that the sex factor FP2 has a density of 1.717 g/cm3 (corresponding to a guanine plus cytosine [G + C] content of 58%) and a mean circular contour length of 28.5 ± 0.6 μm (corresponding to a molecular weight of 59 × 106). Another sex factor FP39 has a density of 1.719 g/cm3 (corresponding to a G + C content of 60%) and a mean circular contour length of 26.5 ± 0.5 μm (corresponding to a molecular weight of 55 × 106). It appears that all, or nearly all, of the FP sex factor deoxyribonucleic acid occurs as covalent circular molecules under the conditions employed. In addition, these procedures have been used to demonstrate that strain PAO, a naturally occurring female (i.e., FP) strain of Pseudomonas aeruginosa, harbors a number of cryptic plasmids having similar densities to the bulk of the cell deoxyribonucleic acid (1.726 g/cm3) and occurring as covalent circular molecules.

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Selected References

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

  1. Chakrabarty A. M., Gunsalus I. C. Autonomous replication of a defective transducing phage in Pseudomonas putida. Virology. 1969 May;38(1):92–104. doi: 10.1016/0042-6822(69)90131-7. [DOI] [PubMed] [Google Scholar]
  2. Clowes R. C. Molecular structure of bacterial plasmids. Bacteriol Rev. 1972 Sep;36(3):361–405. doi: 10.1128/br.36.3.361-405.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. HOLLOWAY B. W. Genetic recombination in Pseudomonas aeruginosa. J Gen Microbiol. 1955 Dec;13(3):572–581. doi: 10.1099/00221287-13-3-572. [DOI] [PubMed] [Google Scholar]
  4. Holloway B. W. Genetics of Pseudomonas. Bacteriol Rev. 1969 Sep;33(3):419–443. doi: 10.1128/br.33.3.419-443.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Lang D. Molecular weights of coliphages and coliphage DNA. 3. Contour length and molecular weight of DNA from bacteriophages T4, T5 and T7, and from bovine papilloma virus. J Mol Biol. 1970 Dec 28;54(3):557–565. doi: 10.1016/0022-2836(70)90126-9. [DOI] [PubMed] [Google Scholar]
  6. Meselson M., Stahl F. W., Vinograd J. EQUILIBRIUM SEDIMENTATION OF MACROMOLECULES IN DENSITY GRADIENTS. Proc Natl Acad Sci U S A. 1957 Jul 15;43(7):581–588. doi: 10.1073/pnas.43.7.581. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Petes T. D., Fangman W. L. Sedimentation properties of yeast chromosomal DNA. Proc Natl Acad Sci U S A. 1972 May;69(5):1188–1191. doi: 10.1073/pnas.69.5.1188. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Radloff R., Bauer W., Vinograd J. A dye-buoyant-density method for the detection and isolation of closed circular duplex DNA: the closed circular DNA in HeLa cells. Proc Natl Acad Sci U S A. 1967 May;57(5):1514–1521. doi: 10.1073/pnas.57.5.1514. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. SCHILDKRAUT C. L., MARMUR J., DOTY P. Determination of the base composition of deoxyribonucleic acid from its buoyant density in CsCl. J Mol Biol. 1962 Jun;4:430–443. doi: 10.1016/s0022-2836(62)80100-4. [DOI] [PubMed] [Google Scholar]
  10. Stanisich V. A., Holloway B. W. A mutant sex factor of Pseudomonas aeruginosa. Genet Res. 1972 Feb;19(1):91–108. doi: 10.1017/s0016672300014294. [DOI] [PubMed] [Google Scholar]
  11. Sykes R. B., Richmond M. H. Intergeneric transfer of a beta-lactamase gene between Ps. aeruginosa and E. coli. Nature. 1970 Jun 6;226(5249):952–954. doi: 10.1038/226952a0. [DOI] [PubMed] [Google Scholar]

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