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. 1995 Mar;177(6):1589–1594. doi: 10.1128/jb.177.6.1589-1594.1995

Streptomycin- and rifampin-resistant mutants of Escherichia coli perturb F exclusion of bacteriophage T7 by affecting synthesis of the F plasmid protein PifA.

C K Schmidt 1, P Kemp 1, I J Molineux 1
PMCID: PMC176777  PMID: 7883717

Abstract

Certain alleles of rpsL that confer resistance to the antibiotic streptomycin almost completely relieve F exclusion of bacteriophage T7. Introduction of a specific rpoB allele conferring resistance to rifampin into the rpsL strain restores the ability of the F-containing strain to exclude T7. This variation in the severity of F exclusion is reflected in the levels of the F-encoded inhibitor protein PifA: F'-containing cells that harbor specific rpsL alleles are phenotypically Pif-, but become Pif+ by the further acquisition of a specific rpoB allele. F-containing cells harboring the gyrA43(Ts) mutation also appear phenotypically Pif-, possibly because repression of the pif operon is enhanced by an altered DNA conformation in the gyrase mutant strain.

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Selected References

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  1. Arnold G. F., Phillips T. A., Tessman I. Levels of DNA topoisomerases, single-stranded-DNA-binding protein, and DNA polymerase I in rho+ and rho-15 strains of Escherichia coli. J Bacteriol. 1989 Sep;171(9):5183–5186. doi: 10.1128/jb.171.9.5183-5186.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Arnold G. F., Tessman I. Regulation of DNA superhelicity by rpoB mutations that suppress defective Rho-mediated transcription termination in Escherichia coli. J Bacteriol. 1988 Sep;170(9):4266–4271. doi: 10.1128/jb.170.9.4266-4271.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Casadaban M. J., Chou J., Cohen S. N. In vitro gene fusions that join an enzymatically active beta-galactosidase segment to amino-terminal fragments of exogenous proteins: Escherichia coli plasmid vectors for the detection and cloning of translational initiation signals. J Bacteriol. 1980 Aug;143(2):971–980. doi: 10.1128/jb.143.2.971-980.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chakrabarti S. L., Gorini L. A link between streptomycin and rifampicin mutation. Proc Natl Acad Sci U S A. 1975 Jun;72(6):2084–2087. doi: 10.1073/pnas.72.6.2084. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Chakrabarti S. L., Gorini L. Interaction between mutations of ribosomes and RNA polymerase: a pair of strA and rif mutants individually temperature-insensitive but temperature-sensitive in combination. Proc Natl Acad Sci U S A. 1977 Mar;74(3):1157–1161. doi: 10.1073/pnas.74.3.1157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chakrabarti S., Gorini L. Growth of bacteriophages MS2 and T7 on streptomycin-resistant mutants of Escherichia coli. J Bacteriol. 1975 Feb;121(2):670–674. doi: 10.1128/jb.121.2.670-674.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Condreay J. P., Molineux I. J. Synthesis of the capsid protein inhibits development of bacteriophage T3 mutants that abortively infect F plasmid-containing cells. J Mol Biol. 1989 Jun 5;207(3):543–554. doi: 10.1016/0022-2836(89)90463-4. [DOI] [PubMed] [Google Scholar]
  8. Cram D., Ray A., Skurray R. Molecular analysis of F plasmid pif region specifying abortive infection of T7 phage. Mol Gen Genet. 1984;197(1):137–142. doi: 10.1007/BF00327934. [DOI] [PubMed] [Google Scholar]
  9. Das A., Court D., Adhya S. Isolation and characterization of conditional lethal mutants of Escherichia coli defective in transcription termination factor rho. Proc Natl Acad Sci U S A. 1976 Jun;73(6):1959–1963. doi: 10.1073/pnas.73.6.1959. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dorman C. J., Barr G. C., Ni Bhriain N., Higgins C. F. DNA supercoiling and the anaerobic and growth phase regulation of tonB gene expression. J Bacteriol. 1988 Jun;170(6):2816–2826. doi: 10.1128/jb.170.6.2816-2826.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Drlica K., Franco R. J., Steck T. R. Rifampin and rpoB mutations can alter DNA supercoiling in Escherichia coli. J Bacteriol. 1988 Oct;170(10):4983–4985. doi: 10.1128/jb.170.10.4983-4985.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Fisher R. F., Yanofsky C. Mutations of the beta subunit of RNA polymerase alter both transcription pausing and transcription termination in the trp operon leader region in vitro. J Biol Chem. 1983 Jul 10;258(13):8146–8150. [PubMed] [Google Scholar]
  13. Galas D. J., Branscomb E. W. Ribosome slowed by mutation to streptomycin resistance. Nature. 1976 Aug 12;262(5569):617–619. doi: 10.1038/262617b0. [DOI] [PubMed] [Google Scholar]
  14. Guarente L. P., Beckwith J. Mutant RNA polymerase of Escherichia coli terminates transcription in strains making defective rho factor. Proc Natl Acad Sci U S A. 1978 Jan;75(1):294–297. doi: 10.1073/pnas.75.1.294. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Inoko H., Shigesada K., Imai M. Isolation and characterization of conditional-lethal rho mutants of Escherichia coli. Proc Natl Acad Sci U S A. 1977 Mar;74(3):1162–1166. doi: 10.1073/pnas.74.3.1162. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Jin D. J., Gross C. A. Characterization of the pleiotropic phenotypes of rifampin-resistant rpoB mutants of Escherichia coli. J Bacteriol. 1989 Sep;171(9):5229–5231. doi: 10.1128/jb.171.9.5229-5231.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kennedy M., Chandler M., Lane D. Mapping and regulation of the pifC promoter of the F plasmid. Biochim Biophys Acta. 1988 May 6;950(1):75–80. doi: 10.1016/0167-4781(88)90075-9. [DOI] [PubMed] [Google Scholar]
  18. Kreuzer K. N., Cozzarelli N. R. Escherichia coli mutants thermosensitive for deoxyribonucleic acid gyrase subunit A: effects on deoxyribonucleic acid replication, transcription, and bacteriophage growth. J Bacteriol. 1979 Nov;140(2):424–435. doi: 10.1128/jb.140.2.424-435.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Miller J. F., Malamy M. H. Identification of the pifC gene and its role in negative control of F factor pif gene expression. J Bacteriol. 1983 Oct;156(1):338–347. doi: 10.1128/jb.156.1.338-347.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Miller J. F., Malamy M. H. Regulation of the F-factor pif operon: pifO, a site required in cis for autoregulation, titrates the pifC product in trans. J Bacteriol. 1984 Oct;160(1):192–198. doi: 10.1128/jb.160.1.192-198.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Molineux I. J. Host-parasite interactions: recent developments in the genetics of abortive phage infections. New Biol. 1991 Mar;3(3):230–236. [PubMed] [Google Scholar]
  22. Molineux I. J., Mooney P. Q., Spence J. L. Recombinants between bacteriophages T7 and T3 which productively infect F-plasmid-containing strains of Escherichia coli. J Virol. 1983 Jun;46(3):881–894. doi: 10.1128/jvi.46.3.881-894.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Molineux I. J., Schmitt C. K., Condreay J. P. Mutants of bacteriophage T7 that escape F restriction. J Mol Biol. 1989 Jun 5;207(3):563–574. doi: 10.1016/0022-2836(89)90465-8. [DOI] [PubMed] [Google Scholar]
  24. Morrison T. G., Malamy M. H. T7 translational control mechanisms and their inhibiton by F factors. Nat New Biol. 1971 May 12;231(19):37–41. doi: 10.1038/newbio231037a0. [DOI] [PubMed] [Google Scholar]
  25. Remes B., Elseviers D. Adenosine 5'-triphosphate leakage does not cause abortive infection of bacteriophage T7 in male Escherichia coli. J Bacteriol. 1980 Aug;143(2):1054–1056. doi: 10.1128/jb.143.2.1054-1056.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Schmitt C. K., Kemp P., Molineux I. J. Genes 1.2 and 10 of bacteriophages T3 and T7 determine the permeability lesions observed in infected cells of Escherichia coli expressing the F plasmid gene pifA. J Bacteriol. 1991 Oct;173(20):6507–6514. doi: 10.1128/jb.173.20.6507-6514.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Schmitt C. K., Molineux I. J. Expression of gene 1.2 and gene 10 of bacteriophage T7 is lethal to F plasmid-containing Escherichia coli. J Bacteriol. 1991 Feb;173(4):1536–1543. doi: 10.1128/jb.173.4.1536-1543.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Shinedling S., Parma D., Gold L. Wild-type bacteriophage T4 is restricted by the lambda rex genes. J Virol. 1987 Dec;61(12):3790–3794. doi: 10.1128/jvi.61.12.3790-3794.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Studier F. W. Relationships among different strains of T7 and among T7-related bacteriophages. Virology. 1979 May;95(1):70–84. doi: 10.1016/0042-6822(79)90402-1. [DOI] [PubMed] [Google Scholar]
  30. Studier F. W. The genetics and physiology of bacteriophage T7. Virology. 1969 Nov;39(3):562–574. doi: 10.1016/0042-6822(69)90104-4. [DOI] [PubMed] [Google Scholar]
  31. Twigg A. J., Sherratt D. Trans-complementable copy-number mutants of plasmid ColE1. Nature. 1980 Jan 10;283(5743):216–218. doi: 10.1038/283216a0. [DOI] [PubMed] [Google Scholar]
  32. Young E. T., Menard R. C. Analysis of the template activity of bacteriophage T7 messenger RNAs during infection of male and female strains of Escherichia coli. J Mol Biol. 1975 Nov 25;99(1):167–184. doi: 10.1016/s0022-2836(75)80166-5. [DOI] [PubMed] [Google Scholar]
  33. Zengel J. M., Young R., Dennis P. P., Nomura M. Role of ribosomal protein S12 in peptide chain elongation: analysis of pleiotropic, streptomycin-resistant mutants of Escherichia coli. J Bacteriol. 1977 Mar;129(3):1320–1329. doi: 10.1128/jb.129.3.1320-1329.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]

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