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. 1973 Nov;116(2):885–892. doi: 10.1128/jb.116.2.885-892.1973

Characterization of Escherichia coli Mutants Tolerant to Bacteriocin JF246: Two New Classes of Tolerant Mutants

John Foulds 1, Constance Barrett 1
PMCID: PMC285459  PMID: 4583254

Abstract

Several hundred independent bacteriocin-tolerant mutants have been isolated without mutagenesis from three strains of Escherichia coli. On the basis of patterns of sensitivity to eight different colicins, over 85% of these mutants could be grouped into four classes. Two classes of mutants, class A and class B, are equivalent to tolA and tolB type mutants. We found tolA and tolB mutants were sensitive to the antibiotic bacitracin. The other two classes of bacteriocin-tolerant mutants, class F and class G, are distinguished from other types of colicin-tolerant mutants on the basis of sensitivity to colicins, dyes, detergents, antibiotics, and chelating agents. The mutation in class F and class G mutants is located between 21 to 23 min on the E. coli chromosome. We propose to designate the loci of these mutations as tolF and tolG, respectively.

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Selected References

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  1. Bernstein A., Rolfe B., Onodera K. Pleiotropic properties and genetic organization of the tolA,B locus of Escherichia coli K-12. J Bacteriol. 1972 Oct;112(1):74–83. doi: 10.1128/jb.112.1.74-83.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. De Haan P. G., Hoekstra W. P., Verhoef C., Felix H. S. Recombination in Escherichia coli. 3. Mapping by the gradient of transmission. Mutat Res. 1969 Nov-Dec;8(3):505–512. doi: 10.1016/0027-5107(69)90067-0. [DOI] [PubMed] [Google Scholar]
  3. Eriksson-Grennberg K. G., Nordström K. Genetics and physiology of a tolE mutant of Escherichia coli K-12 and phenotypic suppression of its phenotype by galactose. J Bacteriol. 1973 Sep;115(3):1219–1222. doi: 10.1128/jb.115.3.1219-1222.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Foulds J. Mode of action of a bacteriocin from Serratia marcescens. J Bacteriol. 1971 Sep;107(3):833–839. doi: 10.1128/jb.107.3.833-839.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Foulds J. Purification and partial characterization of a bacteriocin from Serratia marcescens. J Bacteriol. 1972 Jun;110(3):1001–1009. doi: 10.1128/jb.110.3.1001-1009.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Guterman S. K., Luria S. E. Escherichia coli: strains that excrete an inhibitor of colicin B. Science. 1969 Jun 20;164(3886):1414–1414. doi: 10.1126/science.164.3886.1414. [DOI] [PubMed] [Google Scholar]
  7. Hill C., Holland I. B. Genetic basis of colicin E susceptibility in Escherichia coli. I. Isolation and properties of refractory mutants and the preliminary mapping of their mutations. J Bacteriol. 1967 Sep;94(3):677–686. doi: 10.1128/jb.94.3.677-686.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Holland I. B. Properties of Escherichia coli K12 mutants which show conditional refractivity to colicin E2. J Mol Biol. 1968 Jan 28;31(2):267–275. doi: 10.1016/0022-2836(68)90443-9. [DOI] [PubMed] [Google Scholar]
  9. LENNOX E. S. Transduction of linked genetic characters of the host by bacteriophage P1. Virology. 1955 Jul;1(2):190–206. doi: 10.1016/0042-6822(55)90016-7. [DOI] [PubMed] [Google Scholar]
  10. LOW B., WOOD T. H. A QUICK AND EFFICIENT METHOD FOR INTERRUPTION OF BACTERIAL CONJUGATION. Genet Res. 1965 Jul;6:300–303. doi: 10.1017/s001667230000416x. [DOI] [PubMed] [Google Scholar]
  11. Low B. Formation of merodiploids in matings with a class of Rec- recipient strains of Escherichia coli K12. Proc Natl Acad Sci U S A. 1968 May;60(1):160–167. doi: 10.1073/pnas.60.1.160. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Nagel de Zwaig R., Luria S. E. Genetics and physiology of colicin-tolerant mutants of Escherichia coli. J Bacteriol. 1967 Oct;94(4):1112–1123. doi: 10.1128/jb.94.4.1112-1123.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Nagel de Zwaig R. New class of conditional colicin-tolerant mutants. J Bacteriol. 1969 Jul;99(1):78–84. doi: 10.1128/jb.99.1.78-84.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Nomura M., Witten C. Interaction of colicins with bacterial cells. 3. Colicin-tolerant mutations in Escherichia coli. J Bacteriol. 1967 Oct;94(4):1093–1111. doi: 10.1128/jb.94.4.1093-1111.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Rolfe B., Onodera K. Demonstration of missing membrane proteins in a colicin-tolerant mutant of E. coli K12. Biochem Biophys Res Commun. 1971 Aug 20;44(4):767–773. doi: 10.1016/0006-291x(71)90776-5. [DOI] [PubMed] [Google Scholar]
  16. 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]
  17. Threlfall E. J., Holland I. B. Co-transduction with serB of a pleiotropic mutation affecting colicin E2 refractivity, ultraviolet sensitivity, recombination proficiency and surface properties of Escherichia coli K12. J Gen Microbiol. 1970 Aug;62(3):383–398. doi: 10.1099/00221287-62-3-383. [DOI] [PubMed] [Google Scholar]
  18. VOGEL H. J., BONNER D. M. Acetylornithinase of Escherichia coli: partial purification and some properties. J Biol Chem. 1956 Jan;218(1):97–106. [PubMed] [Google Scholar]
  19. Whitney E. N. The tolC locus in Escherichia coli K12. Genetics. 1971 Jan;67(1):39–53. doi: 10.1093/genetics/67.1.39. [DOI] [PMC free article] [PubMed] [Google Scholar]

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