Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1976 Jul;127(1):51–58. doi: 10.1128/jb.127.1.51-58.1976

Comparative study of R1-specific chromosomal transfer in Escherichia coli K-12 and salmonella typhimurium LT2.

L O Hedén, E Meynell
PMCID: PMC233032  PMID: 776939

Abstract

High-frequency transfer of the chromosomal trp region by R1 observed in Escherichia coli (Pearce and Meynell, 1968) also occurs in Salmonella typhimurium. The reaction is recA independent in both species. The origin of transfer lies within a segment of the chromosome that is inverted in S. typhimurium relative to E. coli, and thus transfer occurs in a different direction in the two species. The character of R1 that is responsible, known as Tfa+, may be lost without affecting other properties of the R factor such as its own transfer.

Full text

PDF
51

Selected References

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

  1. Alfaro G., Willetts N. The relationship between the transfer systems of some bacterial plasmids. Genet Res. 1972 Dec;20(3):279–289. doi: 10.1017/s0016672300013811. [DOI] [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. Brenner D. J., Fanning G. R., Skerman F. J., Falkow S. Polynucleotide sequence divergence among strains of Escherichia coli and closely related organisms. J Bacteriol. 1972 Mar;109(3):953–965. doi: 10.1128/jb.109.3.953-965.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. CLARK A. J., MARGULIES A. D. ISOLATION AND CHARACTERIZATION OF RECOMBINATION-DEFICIENT MUTANTS OF ESCHERICHIA COLI K12. Proc Natl Acad Sci U S A. 1965 Feb;53:451–459. doi: 10.1073/pnas.53.2.451. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Casse F., Pascal M. C., Chippaux M. Comparison between the chromosomal maps of Escherichia coli and Salmonella typhimurium. Length of the inverted segment in the trp region. Mol Gen Genet. 1973 Aug 17;124(3):253–257. doi: 10.1007/BF00293096. [DOI] [PubMed] [Google Scholar]
  6. Chandler P. M., Krishnapillai V. Isolation and properties of recombination-deficient mutants of Pseudomonas aeruginosa. Mutat Res. 1974 Apr;23(1):15–23. doi: 10.1016/0027-5107(74)90155-9. [DOI] [PubMed] [Google Scholar]
  7. Clowes R. C., Moody E. E. Chromosomal transfer from "recombination-deficient" strains of Escherichia coli K-12. Genetics. 1966 Apr;53(4):717–726. doi: 10.1093/genetics/53.4.717. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Coetzee J. N. Chromosome transfer in Proteus mirabilis mediated by hybrid plasmid. J Gen Microbiol. 1975 Jan;86(1):133–146. doi: 10.1099/00221287-86-1-133. [DOI] [PubMed] [Google Scholar]
  9. Cooke M., Meynell E. Chromosomal transfer mediated by de-repressed R factors in F- Escherichia coli K12. Genet Res. 1969 Aug;14(1):79–87. doi: 10.1017/s0016672300001877. [DOI] [PubMed] [Google Scholar]
  10. DEMEREC M., OHTA N. GENETIC ANALYSES OF SALMONELLA TYPHIMURIUM X ESCHERICHIA COLI HYBRIDS. Proc Natl Acad Sci U S A. 1964 Aug;52:317–323. doi: 10.1073/pnas.52.2.317. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gemski P., Jr, Baron L. S., Yamamoto N. Formation of hybrids between coliphage lambda and Salmonella phage P22 with a Salmonella typhimurium hybrid sensitive to these phages. Proc Natl Acad Sci U S A. 1972 Nov;69(11):3110–3114. doi: 10.1073/pnas.69.11.3110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hedén L. O., Rutberg L. R factor-mediated polarized chromosomal transfer in Escherichia coli C. J Bacteriol. 1976 Jul;127(1):46–50. doi: 10.1128/jb.127.1.46-50.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hu S., Ohtsubo E., Davidson N. Electron microscopic heteroduplex studies of sequence relations among plasmids of Escherichia coli: structure of F13 and related F-primes. J Bacteriol. 1975 May;122(2):749–763. doi: 10.1128/jb.122.2.749-763.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hu S., Otsubo E., Davidson N., Saedler H. Electron microscope heteroduplex studies of sequence relations among bacterial plasmids: identification and mapping of the insertion sequences IS1 and IS2 in F and R plasmids. J Bacteriol. 1975 May;122(2):764–775. doi: 10.1128/jb.122.2.764-775.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Johnson E. M., Easterling S. B., Baron L. S. Inefficiency of genetic recombination in hybrids between Escherichia coli and Salmonella typhosa. J Bacteriol. 1971 Apr;106(1):243–249. doi: 10.1128/jb.106.1.243-249.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Moody E. E., Runge R. The integration of autonomous transmissible plasmids into the chromosome of Escherichia coli K12. Genet Res. 1972 Apr;19(2):181–186. doi: 10.1017/s0016672300014427. [DOI] [PubMed] [Google Scholar]
  17. Okada M., Watanabe T., Miyake T. On the nature of the recipient ability of Salmonella typhimurium for foreign deoxyribonucleic acids. J Gen Microbiol. 1968 Feb;50(2):241–252. doi: 10.1099/00221287-50-2-241. [DOI] [PubMed] [Google Scholar]
  18. Pearce L. E., Meynell E. Mutation to high-level streptomycin-resistance in R+ bacteria. J Gen Microbiol. 1968 Jan;50(1):173–176. doi: 10.1099/00221287-50-1-173. [DOI] [PubMed] [Google Scholar]
  19. Pearce L. E., Meynell E. Specific chromosomal affinity of a resistant factor. J Gen Microbiol. 1968 Jan;50(1):159–172. doi: 10.1099/00221287-50-1-159. [DOI] [PubMed] [Google Scholar]
  20. Reeves P., Willetts N. Plasmid specificity of the origin of transfer of sex factor F. J Bacteriol. 1974 Oct;120(1):125–130. doi: 10.1128/jb.120.1.125-130.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. SUGINO Y., HIROTA Y. Conjugal fertility associated with resistance factor R in Escherichia coli. J Bacteriol. 1962 Nov;84:902–910. doi: 10.1128/jb.84.5.902-910.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Sanderson K. E., Hall C. A. F-prime factors of Salmonella typhimurium and an inversion between S. typhimurium and Escherichia coli. Genetics. 1970 Feb;64(2):215–228. doi: 10.1093/genetics/64.2.215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Sanderson K. E. Linkage map of Salmonella typhimurium, edition IV. Bacteriol Rev. 1972 Dec;36(4):558–586. doi: 10.1128/br.36.4.558-586.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Sanderson K. E., Ross H., Ziegler L., Mäkelä P. H. F + , Hfr, and F' strains of Salmonella typhimurium and Salmonella abony. Bacteriol Rev. 1972 Dec;36(4):608–637. doi: 10.1128/br.36.4.608-637.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Scaife J. F-prime factor formation in E. coli K12. Genet Res. 1966 Oct;8(2):189–196. doi: 10.1017/s0016672300010041. [DOI] [PubMed] [Google Scholar]
  26. Signer E. R., Beckwith J. R., Brenner S. Mapping of suppressor loci in Escherichia coli. J Mol Biol. 1965 Nov;14(1):153–166. doi: 10.1016/s0022-2836(65)80237-6. [DOI] [PubMed] [Google Scholar]
  27. Taylor A. L., Trotter C. D. Linkage map of Escherichia coli strain K-12. Bacteriol Rev. 1972 Dec;36(4):504–524. doi: 10.1128/br.36.4.504-524.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Wallace B. J., Pittard J. Regulator gene controlling enzymes concerned in tyrosine biosynthesis in Escherichia coli. J Bacteriol. 1969 Mar;97(3):1234–1241. doi: 10.1128/jb.97.3.1234-1241.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES