Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1969 Jan;97(1):376–385. doi: 10.1128/jb.97.1.376-385.1969

Composite Circular Forms of R Factor Deoxyribonucleic Acid Molecules

Taizo Nisioka 1, Michiko Mitani 1, Royston Clowes 1
PMCID: PMC249615  PMID: 5764338

Abstract

Two R factors, one (R15) conferring resistance to streptomycin and sulfonamide (SMrSUr) and the other (222/R3) to streptomycin, sulfonamide, and chloramphenicol (SMrSUrCMr), were transferred to a Proteus mirabilis strain, and deoxyribonucleic acid (DNA) extracted from these strains was subjected to density-gradient centrifugation. R15-DNA formed a single satellite band at a density of 1.709 g cm−3. Electron microscopy of samples from this band showed circular molecules of one type, with a contour length of 18 μm (35 × 106 daltons). 222/R3-DNA formed a satellite band with three peaks at densities 1.708, 1.711 and 1.717 g cm−3. Electron micrographs revealed circular structures from each band with contour lengths, respectively, of 29 (54 × 106 daltons), 36 (68 × 106 daltons), and 6 μm (12 × 106 daltons). “Supertwisted” forms of several molecular species were found. It is suggested that 222/R3 DNA comprises either a single 36-μm molecule or two individual molecules, 29 and 6 μm in length, and that this may reflect the evolutionary development of R factors.

Full text

PDF
376

Images in this article

Selected References

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

  1. ALFOLDI L., JACOB F., WOLLMAN E. L. Zygose létale dans des croisements entre souches colicinogènes et non colicinogènes d'Escherichia coli. C R Hebd Seances Acad Sci. 1957 Jun 12;244(24):2974–2977. [PubMed] [Google Scholar]
  2. Anderson E. S. Facteurs de transfert et résistance aux antibiotiques chez les entérobactéries. Ann Inst Pasteur (Paris) 1967 May;112(5):547–563. [PubMed] [Google Scholar]
  3. CAVALLI-SFORZA L. L. La sessualità nei batteri. Boll Ist Sieroter Milan. 1950 Sep-Oct;29(9-10):281–289. [PubMed] [Google Scholar]
  4. Falkow S., Citarella R. V., Wohlhieter J. A. The molecular nature of R-factors. J Mol Biol. 1966 May;17(1):102–116. doi: 10.1016/s0022-2836(66)80097-9. [DOI] [PubMed] [Google Scholar]
  5. Gemski P., Jr, Wohlhieter J. A., Baron L. S. Chromosome transfer between Escherichia coli HFR strains and Proteus mirabilis. Proc Natl Acad Sci U S A. 1967 Oct;58(4):1461–1467. doi: 10.1073/pnas.58.4.1461. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. HERSHEY A. D., BURGI E. COMPLEMENTARY STRUCTURE OF INTERACTING SITES AT THE ENDS OF LAMBDA DNA MOLECULES. Proc Natl Acad Sci U S A. 1965 Feb;53:325–328. doi: 10.1073/pnas.53.2.325. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hickson F. T., Roth T. F., Helinski D. R. Circular DNA forms of a bacterial sex factor. Proc Natl Acad Sci U S A. 1967 Oct;58(4):1731–1738. doi: 10.1073/pnas.58.4.1731. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hirota Y. THE EFFECT OF ACRIDINE DYES ON MATING TYPE FACTORS IN ESCHERICHIA COLI. Proc Natl Acad Sci U S A. 1960 Jan;46(1):57–64. doi: 10.1073/pnas.46.1.57. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Lang D., Bujard H., Wolff B., Russell D. Electron microscopy of size and shape of viral DNA in solutions of different ionic strengths. J Mol Biol. 1967 Jan 28;23(2):163–181. doi: 10.1016/s0022-2836(67)80024-x. [DOI] [PubMed] [Google Scholar]
  10. MARMUR J., ROWND R., FALKOW S., BARON L. S., SCHILDKRAUT C., DOTY P. The nature of intergeneric episomal infection. Proc Natl Acad Sci U S A. 1961 Jul 15;47:972–979. doi: 10.1073/pnas.47.7.972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. MONK M., CLOWES R. C. TRANSFER OF THE COLICIN I FACTOR IN ESCHERICHIA COLI K12 AND ITS INTERACTION WITH THE F FERTILITY FACTOR. J Gen Microbiol. 1964 Sep;36:365–384. doi: 10.1099/00221287-36-3-365. [DOI] [PubMed] [Google Scholar]
  12. Meynell E., Meynell G. G., Datta N. Phylogenetic relationships of drug-resistance factors and other transmissible bacterial plasmids. Bacteriol Rev. 1968 Mar;32(1):55–83. doi: 10.1128/br.32.1.55-83.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Rownd R., Nakaya R., Nakamura A. Molecular nature of the drug-resistance factors of the Enterobacteriaceae. J Mol Biol. 1966 Jun;17(2):376–393. doi: 10.1016/s0022-2836(66)80149-3. [DOI] [PubMed] [Google Scholar]
  14. WATANABE T., FUKASAWA T. Episome-mediated transfer of drug resistance in Enterobacteriaceae. I. Transfer of resistance factors by conjugation. J Bacteriol. 1961 May;81:669–678. doi: 10.1128/jb.81.5.669-678.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. WATANABE T., FUKASAWA T. Episome-mediated transfer of drug resistance in Enterobacteriaceae. II. Elimination of resistance factors with acridine dyes. J Bacteriol. 1961 May;81:679–683. doi: 10.1128/jb.81.5.679-683.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. WATANABE T., NISHIDA H., OGATA C., ARAI T., SATO S. EPISOME-MEDIATED TRANSFER OF DRUG RESISTANCE IN ENTEROBACTERIACEAE. VII. TWO TYPES OF NATURALLY OCCURRING R FACTORS. J Bacteriol. 1964 Sep;88:716–726. doi: 10.1128/jb.88.3.716-726.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES