Skip to main content
PMC home page
Microbiological Reviews logoLink to Microbiological Reviews
. 1981 Mar;45(1):52–71. doi: 10.1128/mr.45.1.52-71.1981

Inhibition of bacteriophage replication by extrachromosomal genetic elements.

D H Duckworth, J Glenn, D J McCorquodale
PMCID: PMC281498  PMID: 6452572

Full text

PDF
52

Selected References

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

  1. ADELBERG E. A., BURNS S. N. Genetic variation in the sex factor of Escherichia coli. J Bacteriol. 1960 Mar;79:321–330. doi: 10.1128/jb.79.3.321-330.1960. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Anderson C. W., Eigner J. Breakdown and exclusion of superinfecting T-even bacteriophage in Escherichia coli. J Virol. 1971 Dec;8(6):869–886. doi: 10.1128/jvi.8.6.869-886.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Anderson C. W., Williamson J. R., Eigner J. Localization of parental deoxyribonucleic acid from superinfecting T4 bacteriophage in Escherichia coli. J Virol. 1971 Dec;8(6):887–893. doi: 10.1128/jvi.8.6.887-893.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Anderson E. S. Influence of the delta transfer factor on the phage sensitivity of salmonellae. Nature. 1966 Nov 19;212(5064):795–799. doi: 10.1038/212795a0. [DOI] [PubMed] [Google Scholar]
  5. Anderson E. S. The ecology of transferable drug resistance in the enterobacteria. Annu Rev Microbiol. 1968;22:131–180. doi: 10.1146/annurev.mi.22.100168.001023. [DOI] [PubMed] [Google Scholar]
  6. Anderson E. S., Threlfall E. J., Carr J. M., Savoy L. G. Bacteriophage restriction in Salmonella typhimurium by R factors and transfer factors. J Hyg (Lond) 1973 Sep;71(3):619–631. doi: 10.1017/s0022172400046611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Astrachan L., Miller J. F. Regulation of lambda rex expression after infection of Escherichia coli K by lambda bacteriophage. J Virol. 1972 Mar;9(3):510–518. doi: 10.1128/jvi.9.3.510-518.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. BERTANI G. Lysogenic versus lytic cycle of phage multiplication. Cold Spring Harb Symp Quant Biol. 1953;18:65–70. doi: 10.1101/sqb.1953.018.01.014. [DOI] [PubMed] [Google Scholar]
  9. BERTANI G. Lysogeny. Adv Virus Res. 1958;5:151–193. doi: 10.1016/s0065-3527(08)60673-9. [DOI] [PubMed] [Google Scholar]
  10. BROCK M. L. THE EFFECTS OF POLYAMINES ON THE REPLICATION OF T4RII MUTANTS IN ESCHERICHIA COLI K-12 (LAMBDA). Virology. 1965 Jun;26:221–227. doi: 10.1016/0042-6822(65)90049-8. [DOI] [PubMed] [Google Scholar]
  11. Beckman L. D., Anderson G. C., McCorquodale D. J. Arrangement on the chromosome of the known pre-early genes of bacteriophages T5 and BF23. J Virol. 1973 Nov;12(5):1191–1194. doi: 10.1128/jvi.12.5.1191-1194.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Behnke D., Malke H. Bacteriophage interference in Streptococcus pyogenes. I. Characterization of prophage--host systems interfering with the virulent phage A25. Virology. 1978 Mar;85(1):118–128. doi: 10.1016/0042-6822(78)90416-6. [DOI] [PubMed] [Google Scholar]
  13. Berger E. A. Different mechanisms of energy coupling for the active transport of proline and glutamine in Escherichia coli. Proc Natl Acad Sci U S A. 1973 May;70(5):1514–1518. doi: 10.1073/pnas.70.5.1514. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Berger E. A., Heppel L. A. Different mechanisms of energy coupling for the shock-sensitive and shock-resistant amino acid permeases of Escherichia coli. J Biol Chem. 1974 Dec 25;249(24):7747–7755. [PubMed] [Google Scholar]
  15. Berger H., Kozinski A. W. Suppression of T4D ligase mutations by rIIa and rIIb mutations. Proc Natl Acad Sci U S A. 1969 Nov;64(3):897–904. doi: 10.1073/pnas.64.3.897. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Bertani L. E., Bertani G. Genetics of P2 and related phages. Adv Genet. 1971;16:199–237. doi: 10.1016/s0065-2660(08)60359-4. [DOI] [PubMed] [Google Scholar]
  17. Black L. W., Abremski K. Restriction of phage T4 internal protein I mutants by a strain of Escherichia coli. Virology. 1974 Jul;60(1):180–191. doi: 10.1016/0042-6822(74)90375-4. [DOI] [PubMed] [Google Scholar]
  18. Black L. W. Bacteriophage T4 internal protein mutants: isolation and properties. Virology. 1974 Jul;60(1):166–179. doi: 10.1016/0042-6822(74)90374-2. [DOI] [PubMed] [Google Scholar]
  19. Blumberg D. D., Mabie C. T., Malamy M. H. T7 protein synthesis in F-factor-containing cells: evidence for an episomally induced impairment of translation and relation to an alteration in membrane permeability. J Virol. 1975 Jan;17(1):94–105. doi: 10.1128/jvi.17.1.94-105.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Blumberg D. D., Malamy M. H. Evidence for the presence of nontranslated T7 late mRNA in infected F'(PIF+) episome-containing cells. J Virol. 1974 Feb;13(2):378–385. doi: 10.1128/jvi.13.2.378-385.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Bode W. Lysis inhibition in Escherichia coli infected with bacteriophage T4. J Virol. 1967 Oct;1(5):948–955. doi: 10.1128/jvi.1.5.948-955.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Britton J. R., Haselkorn R. Macromolecular synthesis in T7 infected F' cells. Virology. 1975 Sep;67(1):264–275. doi: 10.1016/0042-6822(75)90423-7. [DOI] [PubMed] [Google Scholar]
  23. Britton J. R., Haselkorn R. Permeability lesions in male Escherichia coli infected with bacteriophage T7. Proc Natl Acad Sci U S A. 1975 Jun;72(6):2222–2226. doi: 10.1073/pnas.72.6.2222. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Brégégère F. Bacteriophage P2-lambda interference. III. Essential role of an early step in the initiation of lambda replication. J Mol Biol. 1978 Jun 25;122(2):113–125. doi: 10.1016/0022-2836(78)90029-3. [DOI] [PubMed] [Google Scholar]
  25. Buller C. S., Astrachan L. Replication of T4rII bacteriophage in Escherichia coli K-12 (lambda). J Virol. 1968 Apr;2(4):298–307. doi: 10.1128/jvi.2.4.298-307.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. 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]
  27. Cheung A. K., Duckworth D. H. Membrane damage in abortive infections of colicin Ib-containing Escherichia coli by bacteriophage T5. J Virol. 1977 Jul;23(1):98–105. doi: 10.1128/jvi.23.1.98-105.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Christensen J. R., Geiman J. M. A new effect of the rex gene of phage lambda: premature lysis after infection by phage T1. Virology. 1973 Nov;56(1):285–290. doi: 10.1016/0042-6822(73)90306-1. [DOI] [PubMed] [Google Scholar]
  29. Cohen S. N., Chang A. C. Genetic expression in bacteriophage lambda. IV. Effects of P2 prophage on lambda inhibition of host synthesis and lambda gene expression. Virology. 1971 Nov;46(2):387–406. doi: 10.1016/0042-6822(71)90041-9. [DOI] [PubMed] [Google Scholar]
  30. Condit R. C. F factor-mediated inhibition of bacteriophage T7 growth: increased membrane permeability and decreased ATP levels following T7 infection of male Escherichia coli. J Mol Biol. 1975 Oct 15;98(1):45–59. doi: 10.1016/s0022-2836(75)80100-8. [DOI] [PubMed] [Google Scholar]
  31. Condit R. C., Steitz J. A. F factor-mediated inhibition of bacteriophage T7 growth: analysis of T7 RNA and protein synthesis in vivo and in vitro using male and female Escherichia coli. J Mol Biol. 1975 Oct 15;98(1):31–43. doi: 10.1016/s0022-2836(75)80099-4. [DOI] [PubMed] [Google Scholar]
  32. Cuzin F. Un bactériophage spécifique du type sexuel F- d'Escherichia coli K 12. C R Acad Sci Hebd Seances Acad Sci D. 1965 Jun 14;260(24):6482–6485. [PubMed] [Google Scholar]
  33. DULBECCO R. Mutual exclusion between related phages. J Bacteriol. 1952 Feb;63(2):209–217. doi: 10.1128/jb.63.2.209-217.1952. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Dhillon E. K., Dhillon T. S. HK239: a P2 related temperate phage which excludes rII mutants of T4. Virology. 1973 Sep;55(1):136–142. doi: 10.1016/s0042-6822(73)81015-3. [DOI] [PubMed] [Google Scholar]
  35. Duberstein R., Oeschger M. P. Growth of bacteriophage H on male and female strains of Escherichia coli. J Virol. 1973 Mar;11(3):460–463. doi: 10.1128/jvi.11.3.460-463.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Duckworth D. H., Dunn G. B., McCorquodale D. J. Identification of the gene controlling the synthesis of the major bacteriophage T5 membrane protein. J Virol. 1976 May;18(2):542–549. doi: 10.1128/jvi.18.2.542-549.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Ebel-Tsipis J., Botstein D. Superinfection exclusion by P22 prophage in lysogens of Salmonella typhimurium. 1. Exclusion of generalized transducing particles. Virology. 1971 Sep;45(3):629–637. doi: 10.1016/0042-6822(71)90177-2. [DOI] [PubMed] [Google Scholar]
  38. Ennis H. L., Kievitt K. D. Association of the rIIA protein with the bacterial membrane. Proc Natl Acad Sci U S A. 1973 May;70(5):1468–1472. doi: 10.1073/pnas.70.5.1468. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Epstein W., Kim B. S. Potassium transport loci in Escherichia coli K-12. J Bacteriol. 1971 Nov;108(2):639–644. doi: 10.1128/jb.108.2.639-644.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. FREDERICQ P. Action bactéricide du bactériophage T.6 sur une souche microbienne ne permettant pas sa multiplication. C R Seances Soc Biol Fil. 1952 May;146(9-10):800–803. [PubMed] [Google Scholar]
  41. FREDERICQ P. Colicins. Annu Rev Microbiol. 1957;11:7–22. doi: 10.1146/annurev.mi.11.100157.000255. [DOI] [PubMed] [Google Scholar]
  42. Fields K. L. Comparison of the action of colicins E1 and K on Escherichia coli with the effects of abortive infection by virulent bacteriophages. J Bacteriol. 1969 Jan;97(1):78–82. doi: 10.1128/jb.97.1.78-82.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. GAREN A. Physiological effects of rII mutations in bacteriophage T4. Virology. 1961 Jun;14:151–163. doi: 10.1016/0042-6822(61)90190-8. [DOI] [PubMed] [Google Scholar]
  44. Glenn J., Cheung A. K., Duckworth D. H. Are class I (pre-early) proteins of bacteriophage T5 sufficient to induce abortive infection of ColIb+ Escherichia coli? J Virol. 1979 May;30(2):431–437. doi: 10.1128/jvi.30.2.431-437.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Glenn J., Duckworth D. H. Amino acid and sugar transport in Escherichia coli (ColIb) during abortive infection by bacteriophage T5. J Virol. 1979 May;30(2):421–430. doi: 10.1128/jvi.30.2.421-430.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Glenn J., Duckworth D. H. Fluorescence changes of a membrane-bound dye during bacteriophage T5 infection of Escherichia coli. J Virol. 1980 Jan;33(1):553–556. doi: 10.1128/jvi.33.1.553-556.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Glenn J., Duckworth D. H. Ion fluxes during T5 bacteriophage infection of Escherichia coli. Arch Biochem Biophys. 1980 May;201(2):576–585. doi: 10.1016/0003-9861(80)90547-0. [DOI] [PubMed] [Google Scholar]
  48. Gussin G. N., Peterson V. Isolation and properties of rex - mutants of bacteriophage lambda. J Virol. 1972 Oct;10(4):760–765. doi: 10.1128/jvi.10.4.760-765.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Guterman S. K. Colicin B: mode of action and inhibition by enterochelin. J Bacteriol. 1973 Jun;114(3):1217–1224. doi: 10.1128/jb.114.3.1217-1224.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Gómez B., Nualart L. Requirement of the bacteriopahge T7 0.7 gene for phage growth in the presence of the Col 1b factor. J Gen Virol. 1977 Apr;35(1):99–106. doi: 10.1099/0022-1317-35-1-99. [DOI] [PubMed] [Google Scholar]
  51. HAKURA A., OTSUJI N., HIROTA Y. A TEMPERATE PHAGE SPECIFIC FOR FEMALE STRAINS OF ESCHERICHIA COLI K 12. J Gen Microbiol. 1964 Apr;35:69–73. doi: 10.1099/00221287-35-1-69. [DOI] [PubMed] [Google Scholar]
  52. HOFFEE P., ENGLESBERG E., LAMY F. THE GLUCOSE PERMEASE SYSTEM IN BACTERIA. Biochim Biophys Acta. 1964 Mar 30;79:337–350. [PubMed] [Google Scholar]
  53. Hardy K. G. Colicinogeny and related phenomena. Bacteriol Rev. 1975 Dec;39(4):464–515. doi: 10.1128/br.39.4.464-515.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Hausmann R. The genetics of T-odd phages. Annu Rev Microbiol. 1973;27:51–67. doi: 10.1146/annurev.mi.27.100173.000411. [DOI] [PubMed] [Google Scholar]
  55. Havekes L. M., Lugtenberg B. J., Hoekstra W. P. Conjugation deficient E. coli K12 F- mutants with heptose-less lipopolysaccharide. Mol Gen Genet. 1976 Jul 5;146(1):43–50. doi: 10.1007/BF00267981. [DOI] [PubMed] [Google Scholar]
  56. Hedges R. W., Datta N., Coetzee J. N., Dennison S. R factors from Proteus morganii. J Gen Microbiol. 1973 Aug;77(2):249–259. doi: 10.1099/00221287-77-2-249. [DOI] [PubMed] [Google Scholar]
  57. Helgerson S. L., Cramer W. A. Changes in E. coli cell envelope structure caused by uncouplers of active transport and colicin E1. J Supramol Struct. 1976;5(3):291–308. doi: 10.1002/jss.400050304. [DOI] [PubMed] [Google Scholar]
  58. Hemphill H. E., Whiteley H. R. Bacteriophages of Bacillus subtilis. Bacteriol Rev. 1975 Sep;39(3):257–315. doi: 10.1128/br.39.3.257-315.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Herman R. C., Moyer R. W. In vivo repair of bacteriophage t5 DNA: an assay for viral growth control. Virology. 1975 Aug;66(2):393–407. doi: 10.1016/0042-6822(75)90212-3. [DOI] [PubMed] [Google Scholar]
  60. Herman R. C., Moyer R. W. In vivo repair of the single-strand interruptions contained in bacteriophage T5 DNA. Proc Natl Acad Sci U S A. 1974 Mar;71(3):680–684. doi: 10.1073/pnas.71.3.680. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Howard B. D. Phage lambda mutants deficient in r-II exclusion. Science. 1967 Dec 22;158(3808):1588–1589. doi: 10.1126/science.158.3808.1588. [DOI] [PubMed] [Google Scholar]
  62. Hughes V., Meynell G. G. The contribution of plasmid and host genes to plasmid-mediated interference with phage growth. Genet Res. 1977 Oct;30(2):179–185. doi: 10.1017/s0016672300017572. [DOI] [PubMed] [Google Scholar]
  63. Hull R., Moody E. E. Isolation and genetic characterizaion of Escherichia coli K-12 mutations affecting bacteriophage T5 restriction by the ColIb plasmid. J Bacteriol. 1976 Jul;127(1):229–236. doi: 10.1128/jb.127.1.229-236.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  64. Hyman R. W., Brunovskis I., Summers W. C. A biochemical comparison of the related bacteriophages T7, phiI, phiII, W31, H, and T3. Virology. 1974 Jan;57(1):189–206. doi: 10.1016/0042-6822(74)90120-2. [DOI] [PubMed] [Google Scholar]
  65. Jacquemin-Sablon A., Lanni Y. T. Lambda-repressed mutants of bacteriophage T5. I. Isolation and genetical characterization. Virology. 1973 Nov;56(1):230–237. doi: 10.1016/0042-6822(73)90302-4. [DOI] [PubMed] [Google Scholar]
  66. Jetten A. M. Effects of colicins K and E1 on the glucose phosphotransferase system. Biochim Biophys Acta. 1976 Aug 13;440(2):403–411. doi: 10.1016/0005-2728(76)90074-8. [DOI] [PubMed] [Google Scholar]
  67. KAISER A. D., JACOB F. Recombination between related temperate bacteriophages and the genetic control of immunity and prophage localization. Virology. 1957 Dec;4(3):509–521. doi: 10.1016/0042-6822(57)90083-1. [DOI] [PubMed] [Google Scholar]
  68. KOZAKA M., MATSUBARA K., TAKAGI Y. On the regulatory mechanism of synthesis of early enzyme induced by bacteriophage T4. Biochem Biophys Res Commun. 1963 May 3;11:244–248. doi: 10.1016/0006-291x(63)90342-5. [DOI] [PubMed] [Google Scholar]
  69. Karam J. D., Barker B. Properties of bacteriophage T4 mutants defective in gene 30 (deoxyribonucleic acid ligase) and the rII gene. J Virol. 1971 Feb;7(2):260–266. doi: 10.1128/jvi.7.2.260-266.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  70. Kerszman G., Glover S. W., Aronovitch J. The restriction of bacteriophage lambda in Escherichia coli strain w. J Gen Virol. 1967 Jul;1(3):333–347. doi: 10.1099/0022-1317-1-3-333. [DOI] [PubMed] [Google Scholar]
  71. Knopf K., Bujard H. Structure and function of the genome of coliphage T5. Transcription in vitro of the "nicked" and "nick-free" T5+ DNA. Eur J Biochem. 1975 May 6;53(2):371–385. doi: 10.1111/j.1432-1033.1975.tb04077.x. [DOI] [PubMed] [Google Scholar]
  72. Koerner J. F., Snustad D. P. Shutoff of host macromolecular synthesis after T-even bacteriophage infection. Microbiol Rev. 1979 Jun;43(2):199–223. doi: 10.1128/mr.43.2.199-223.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  73. Kopecky A. L., Copeland D. P., Lusk J. E. Viability of Escherichia coli treated with colicin K. Proc Natl Acad Sci U S A. 1975 Nov;72(11):4631–4634. doi: 10.1073/pnas.72.11.4631. [DOI] [PMC free article] [PubMed] [Google Scholar]
  74. Krylov V. N. Possible function of rII genes of bacteriophage T4. Virology. 1970 Aug;41(4):711–717. doi: 10.1016/0042-6822(70)90435-6. [DOI] [PubMed] [Google Scholar]
  75. LEDERBERG S. Suppression of the multiplication of heterologous bacteriophages in lysogenic bacteria. Virology. 1957 Jun;3(3):496–513. doi: 10.1016/0042-6822(57)90006-5. [DOI] [PubMed] [Google Scholar]
  76. LURIA S. E. ON THE MECHANISMS OF ACTION OF COLICINS. Ann Inst Pasteur (Paris) 1964 Nov;107:SUPPL–SUPPL:73. [PubMed] [Google Scholar]
  77. Lanni Y. T. DNA transfer from phage T5 to host cells: dependence on intercurrent protein synthesis. Proc Natl Acad Sci U S A. 1965 May;53(5):969–973. doi: 10.1073/pnas.53.5.969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  78. Lanni Y. T. First-step-transfer deoxyribonucleic acid of bacteriophage T5. Bacteriol Rev. 1968 Sep;32(3):227–242. doi: 10.1128/br.32.3.227-242.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  79. Lanni Y. Functions of two genes in the first-step-transfer DNA of bacteriophage T5. J Mol Biol. 1969 Aug 28;44(1):173–183. doi: 10.1016/0022-2836(69)90412-4. [DOI] [PubMed] [Google Scholar]
  80. Levisohn R., Konisky J., Nomura M. Interaction of colicins with bacterial cells. IV. Immunity breakdown studied with colicins Ia and Ib. J Bacteriol. 1968 Sep;96(3):811–821. doi: 10.1128/jb.96.3.811-821.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  81. Lindahl G., Sironi G., Bialy H., Calendar R. Bacteriophage lambda; abortive infection of bacteria lysogenic for phage P2. Proc Natl Acad Sci U S A. 1970 Jul;66(3):587–594. doi: 10.1073/pnas.66.3.587. [DOI] [PMC free article] [PubMed] [Google Scholar]
  82. Linial M., Malamy M. H. Studies with bacteriophage phi II. Events following infection of male and female derivatives of Escherichia coli K-12. J Virol. 1970 Jan;5(1):72–78. doi: 10.1128/jvi.5.1.72-78.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  83. Luria S. E. Colicins and the energetics of cell membranes. Sci Am. 1975 Dec;233(6):30–37. doi: 10.1038/scientificamerican1275-30. [DOI] [PubMed] [Google Scholar]
  84. MAEKELAE O., MAEKELAE P. H., SOIKKELI S. SEX-SPECIFICITY OF THE BACTERIOPHAGE T7. Ann Med Exp Biol Fenn. 1964;42:188–195. [PubMed] [Google Scholar]
  85. Males B. M., Stocker B. A. Escherichia coli K317, formerly used to define colicin group E2, produces colicin E7, is immune to colicin E2, and carries a bacteriophage-restricting conjugative plasmid. J Bacteriol. 1980 Nov;144(2):524–531. doi: 10.1128/jb.144.2.524-531.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  86. Mark K. K., Szybalski W. Repressor and rex product of coliphage lambda: lack of collaboration and joint controls. Mol Gen Genet. 1973;123(2):123–134. doi: 10.1007/BF00267329. [DOI] [PubMed] [Google Scholar]
  87. Mattson T., Russel M. The time of synthesis and function of the rII + product of bacteriophage T4. Virology. 1972 Jul;49(1):160–167. doi: 10.1016/s0042-6822(72)80017-5. [DOI] [PubMed] [Google Scholar]
  88. McCorquodale D. J., Buchanan J. M. Patterns of protein synthesis in T5-infected Escherichia coli. J Biol Chem. 1968 May 25;243(10):2550–2559. [PubMed] [Google Scholar]
  89. McCorquodale D. J., Lanni Y. T. Patterns of protein synthesis in Escherichia coli infected by amber mutants in the first-step-transfer DNA of T5. J Mol Biol. 1970 Feb 28;48(1):133–143. doi: 10.1016/0022-2836(70)90224-x. [DOI] [PubMed] [Google Scholar]
  90. McCorquodale D. J., Shaw A. R., Shaw P. K., Chinnadurai G. Pre-early polypeptides of bacteriophages T5 and BF23. J Virol. 1977 May;22(2):480–488. doi: 10.1128/jvi.22.2.480-488.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  91. McCorquodale D. J. The T-odd bacteriophages. CRC Crit Rev Microbiol. 1975 Dec;4(2):101–159. doi: 10.3109/10408417509111574. [DOI] [PubMed] [Google Scholar]
  92. Meselson M., Yuan R., Heywood J. Restriction and modification of DNA. Annu Rev Biochem. 1972;41:447–466. doi: 10.1146/annurev.bi.41.070172.002311. [DOI] [PubMed] [Google Scholar]
  93. 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]
  94. Mizobuchi K., Anderson G. C., McCorquodale D. J. Abortive infection by bacteriophage BF23 due to the colicin Ib factor. I. Genetic studies of nonrestricted and amber mutants of bacteriophage BF23. Genetics. 1971 Jul;68(3):323–340. doi: 10.1093/genetics/68.3.323. [DOI] [PMC free article] [PubMed] [Google Scholar]
  95. Mizobuchi K., McCorquodale D. J. Abortive infection by bacteriophage BF23 due to the colicin Ib factor. II. Involvement of pre-early proteins. J Mol Biol. 1974 May 5;85(1):67–74. doi: 10.1016/0022-2836(74)90129-6. [DOI] [PubMed] [Google Scholar]
  96. Molnar D. M., Lawton W. D. Pasteurella Bacteriophage Sex Specific in Escherichia coli. J Virol. 1969 Dec;4(6):896–900. doi: 10.1128/jvi.4.6.896-900.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  97. Morrison T. G., Blumberg D. D., Malamy M. H. T7 protein synthesis in F' episome-containing cells: assignment of specific proteins to three translational groups. J Virol. 1974 Feb;13(2):386–393. doi: 10.1128/jvi.13.2.386-393.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  98. 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]
  99. Moyer R. W., Fu A. S., Szabo C. Regulation of bacteriophage T5 development by ColI factors. J Virol. 1972 May;9(5):804–812. doi: 10.1128/jvi.9.5.804-812.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  100. NOMURA M. DNA synthesized in Escherichia coli K12 (lambda) after infection with an rII mutant of bacteriophage T4. Virology. 1961 Jun;14:164–166. doi: 10.1016/0042-6822(61)90191-x. [DOI] [PubMed] [Google Scholar]
  101. Nieva-Gomez D., Konisky J. Membrane changes in Escherichia coli induced by colicin Ia and agents known to disrupt energy transduction. Biochemistry. 1976 Jun 29;15(13):2747–2753. doi: 10.1021/bi00658a006. [DOI] [PubMed] [Google Scholar]
  102. Nisioka T., Ozeki H. Early abortive lysis by phage BF23 in Escherichia coli K-12 carrying the colicin Ib factor. J Virol. 1968 Nov;2(11):1249–1254. doi: 10.1128/jvi.2.11.1249-1254.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  103. Peterson R. F., Kievitt K. D., Ennis H. L. Membrane protein synthesis after infection of Escherichia coli B with phage T4: the rIIB protein. Virology. 1972 Nov;50(2):520–527. doi: 10.1016/0042-6822(72)90403-5. [DOI] [PubMed] [Google Scholar]
  104. Phillips S. K., Cramer W. A. Properties of the fluorescence probe response associated with the transmission mechanism of colicin E1. Biochemistry. 1973 Mar 13;12(6):1170–1176. doi: 10.1021/bi00730a024. [DOI] [PubMed] [Google Scholar]
  105. Pizer L. I., Smith H. S., Miovic M., Pylkas L. Effect of prophage W on the propagation of bacteriophages T2 and T4. J Virol. 1968 Nov;2(11):1339–1345. doi: 10.1128/jvi.2.11.1339-1345.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  106. Plate C. A., Suit J. L., Jetten A. M., Luria S. E. Effects of colicin K on a mutant of Escherichia coli deficient in Ca 2+, Mg 2+-activated adenosine triphosphatase. J Biol Chem. 1974 Oct 10;249(19):6138–6143. [PubMed] [Google Scholar]
  107. Ponta H., Pon C. L., Herrlich P., Gualerzi C., Hirsch-Kauffmann M., Pfennig-Yeh M. l., rahmsdorf H. J., Schweiger M. The sex-factor-dependent exclusion of coli virus T7. Eur J Biochem. 1975 Nov 1;59(1):261–270. doi: 10.1111/j.1432-1033.1975.tb02450.x. [DOI] [PubMed] [Google Scholar]
  108. Price K. E., DeFuria M. D., Pursiano T. A. Amikacin, an aminoglycoside with marked activity against antibiotic-resistant clinical isolates. J Infect Dis. 1976 Nov;134(Suppl):S249–S261. doi: 10.1093/infdis/135.supplement_2.s249. [DOI] [PubMed] [Google Scholar]
  109. RUTBERG L., RUTBERG B. ON THE EXPRESSION OF THE RII MUTATION OF T-EVEN BACTERIOPHAGES IN ESCHERICHIA COLI STRAIN B. Virology. 1964 Feb;22:280–283. doi: 10.1016/0042-6822(64)90013-3. [DOI] [PubMed] [Google Scholar]
  110. Rao R. N. Bacteriophage P22 controlled exclusion in Salmonella typhimurium. J Mol Biol. 1968 Aug 14;35(3):607–622. doi: 10.1016/s0022-2836(68)80017-8. [DOI] [PubMed] [Google Scholar]
  111. Ravin V. K., Shulga M. G. Evidence for extrachromosomal location of prophage N15. Virology. 1970 Apr;40(4):800–807. doi: 10.1016/0042-6822(70)90125-x. [DOI] [PubMed] [Google Scholar]
  112. 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]
  113. Rettenmier C. W., Hemphill H. E. Abortive infection of lysogenic Bacillus subtilis 168(SPO2) by bacteriophage phi 1. J Virol. 1974 Apr;13(4):870–880. doi: 10.1128/jvi.13.4.870-880.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  114. Rettenmier C. W., Hemphill H. E. Prophage-mediated interference affecting the development of Bacillus subtilis bacteriophage phi e. J Virol. 1973 Mar;11(3):372–377. doi: 10.1128/jvi.11.3.372-377.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  115. Revel H. R., Georgopoulos C. P. Restriction of nonglucosylated T-even bacteriophages by prophage P1. Virology. 1969 Sep;39(1):1–17. doi: 10.1016/0042-6822(69)90343-2. [DOI] [PubMed] [Google Scholar]
  116. Rogers S. G., Godwin E. A., Shinosky E. S., Rhoades M. Interruption-deficient mutants of bacteriophage T5 I. Isolation and general properties. J Virol. 1979 Feb;29(2):716–725. doi: 10.1128/jvi.29.2.716-725.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  117. Rutberg B., Rutberg L. Bacteriophage-induced functions in Escherichia coli K (lambda) infected with rII mutants of bacteriophage T4. J Bacteriol. 1966 Jan;91(1):76–80. doi: 10.1128/jb.91.1.76-80.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  118. Sauerbier W., Puck S. M., Bräutigam A. R., Hirsch-Kauffmann M. Control of gene function in bacteriophage T4. I. Ribonucleic acid and deoxyribonucleic acid metabolism in T4rII-infected lambda-lysogenic hosts. J Virol. 1969 Nov;4(5):742–752. doi: 10.1128/jvi.4.5.742-752.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  119. Schein S. J., Kagan B. L., Finkelstein A. Colicin K acts by forming voltage-dependent channels in phospholipid bilayer membranes. Nature. 1978 Nov 9;276(5684):159–163. doi: 10.1038/276159a0. [DOI] [PubMed] [Google Scholar]
  120. Schnaitman C., Smith D., de Salsas M. F. Temperate Bacteriophage Which Causes the Production of a New Major Outer Membrane Protein by Escherichia coli. J Virol. 1975 May;15(5):1121–1130. doi: 10.1128/jvi.15.5.1121-1130.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  121. Sekiguchi M. Studies on the physiological defect in rII mutants of bacteriophage T4. J Mol Biol. 1966 Apr;16(2):503–522. doi: 10.1016/s0022-2836(66)80188-2. [DOI] [PubMed] [Google Scholar]
  122. Selzer G., Bolle A., Krisch B., Epstein R. Construction and properties of recombinant plasmids containing the rII genes of bacteriophage T4. Mol Gen Genet. 1978 Feb 27;159(3):301–309. doi: 10.1007/BF00268267. [DOI] [PubMed] [Google Scholar]
  123. Sironi G., Bialy H., Lozeron H. A., Calendar R. Bacteriophage P2: interaction with phage lambda and with recombination-deficient bacteria. Virology. 1971 Nov;46(2):387–396. doi: 10.1016/0042-6822(71)90040-7. [DOI] [PubMed] [Google Scholar]
  124. Smith H. S., Pizer L. I. Abortive infection of Escherichia coli strain W by T2 bacteriophage. J Mol Biol. 1968 Oct 14;37(1):131–149. doi: 10.1016/0022-2836(68)90078-8. [DOI] [PubMed] [Google Scholar]
  125. Smith H. S., Pizer L. I., Pylkas L., Lederberg S. Abortive infection of Shigella dysenteriae P2 by T2 bacteriophage. J Virol. 1969 Aug;4(2):162–168. doi: 10.1128/jvi.4.2.162-168.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  126. Strobel M., Nomura M. Restriction of the growth of bacteriophage BF23 by a colicine I (Col I-P9) factor. Virology. 1966 Apr;28(4):763–765. doi: 10.1016/0042-6822(66)90263-7. [DOI] [PubMed] [Google Scholar]
  127. Susskind M. M., Botstein D. Molecular genetics of bacteriophage P22. Microbiol Rev. 1978 Jun;42(2):385–413. doi: 10.1128/mr.42.2.385-413.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  128. Susskind M. M., Botstein D., Wright A. Superinfection exclusion by P22 prophage in lysogens of Salmonella typhimurium. III. Failure of superinfecting phage DNA to enter sieA+ lysogens. Virology. 1974 Dec;62(2):350–366. doi: 10.1016/0042-6822(74)90398-5. [DOI] [PubMed] [Google Scholar]
  129. Susskind M. M., Wright A., Botstein D. Superinfection exclusion by P22 prophage in lysogens of Salmonella typhimurium. II. Genetic evidence for two exclusion systems. Virology. 1971 Sep;45(3):638–652. doi: 10.1016/0042-6822(71)90178-4. [DOI] [PubMed] [Google Scholar]
  130. Susskind M. M., Wright A., Botstein D. Superinfection exclusion by P22 prophage in lysogens of Salmonella typhimurium. IV. Genetics and physiology of sieB exclusion. Virology. 1974 Dec;62(2):367–384. doi: 10.1016/0042-6822(74)90399-7. [DOI] [PubMed] [Google Scholar]
  131. Szabo C., Dharmgrongartama B., Moyer R. W. The regulation of transcription in bacteriophage T5-infected Escherichia coli. Biochemistry. 1975 Mar 11;14(5):989–997. doi: 10.1021/bi00676a018. [DOI] [PubMed] [Google Scholar]
  132. Szabo C., Moyer R. W. Purification and properties of a bacteriophage T5-modified form of Escherichia coli RNA polymerase. J Virol. 1975 Apr;15(4):1042–1046. doi: 10.1128/jvi.15.4.1042-1046.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  133. Takeishi K., Kaji A. Presence of active polyribosomes in bacterial cells infected with T4 bacteriophage ghosts. J Virol. 1975 Jul;16(1):62–69. doi: 10.1128/jvi.16.1.62-69.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  134. Taylor D. E., Grant R. B. Incompatibility and bacteriophage inhibition properties of N-1, a plasmid belonging to the H2 incompatibility group. Mol Gen Genet. 1977 May 20;153(1):5–10. doi: 10.1007/BF01035990. [DOI] [PubMed] [Google Scholar]
  135. Taylor D. E., Grant R. B. Inhibition of bacteriophage lambda, T1, and T7 development by R plasmids of the H incompatibility group. Antimicrob Agents Chemother. 1976 Oct;10(4):762–764. doi: 10.1128/aac.10.4.762. [DOI] [PMC free article] [PubMed] [Google Scholar]
  136. Tokuda H., Konisky J. Mode of action of colicin Ia: effect of colicin on the Escherichia coli proton electrochemical gradient. Proc Natl Acad Sci U S A. 1978 Jun;75(6):2579–2583. doi: 10.1073/pnas.75.6.2579. [DOI] [PMC free article] [PubMed] [Google Scholar]
  137. Tomizawa J., Ogawa T. Inhibition of growth of rII mutants of bacteriophage T4 by immunity substance of bacteriophage lambda. J Mol Biol. 1967 Jan 28;23(2):277–280. doi: 10.1016/s0022-2836(67)80033-0. [DOI] [PubMed] [Google Scholar]
  138. UETAKE H., LURIA S. E., BURROUS J. W. Conversion of somatic antigens in Salmonella by phage infection leading to lysis or lysogeny. Virology. 1958 Feb;5(1):68–91. doi: 10.1016/0042-6822(58)90006-0. [DOI] [PubMed] [Google Scholar]
  139. Verhoef C., Lugtenberg B., van Boxtel R., de Graaff P., Verheij H. Genetics and biochemistry of the peptidoglycan-associated proteins b and c of Escherichia coli K12. Mol Gen Genet. 1979 Jan 31;169(2):137–146. doi: 10.1007/BF00271664. [DOI] [PubMed] [Google Scholar]
  140. 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]
  141. WATANABE T., OKADA M. NEW TYPE OF SEX FACTOR-SPECIFIC BACTERIOPHAGE OF ESCHERICHIA COLI. J Bacteriol. 1964 Mar;87:727–736. doi: 10.1128/jb.87.3.727-736.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  142. WHITFIELD J. F. The effect of carriage of P2 prophage on infections with phages of the T5 group. J Bacteriol. 1955 Jul;70(1):125–126. doi: 10.1128/jb.70.1.125-126.1955. [DOI] [PMC free article] [PubMed] [Google Scholar]
  143. Watanabe T., Takano T., Arai T., Nishida H., Sato S. Episome-mediated Transfer of Drug Resistance in Enterobacteriaceae X. Restriction and Modification of Phages by fi R Factors. J Bacteriol. 1966 Aug;92(2):477–486. doi: 10.1128/jb.92.2.477-486.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  144. Weintraub S. B., Frankel F. R. Identification of the T4rIIB gene product as a membrane protein. J Mol Biol. 1972 Oct 14;70(3):589–615. doi: 10.1016/0022-2836(72)90561-x. [DOI] [PubMed] [Google Scholar]
  145. Wendt L. Mechanism of colicin action: early events. J Bacteriol. 1970 Dec;104(3):1236–1241. doi: 10.1128/jb.104.3.1236-1241.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  146. Whitaker P. A., Yamada Y., Nakada D. F-Factor-mediated restriction of bacteriophage T7: synthesis of RNA and protein in T7-infected Escherichia coli F- and F+ cells. J Virol. 1975 Dec;16(6):1380–1390. doi: 10.1128/jvi.16.6.1380-1390.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  147. Williams L., Meynell G. G. Female-specific phages and F-minus strains of Escherichia coli K12. Mol Gen Genet. 1971;113(3):222–227. doi: 10.1007/BF00339542. [DOI] [PubMed] [Google Scholar]
  148. Yamada Y., Nakada D. F-Factor-mediated restriction of bacteriophage T7: protein synthesis in cell-free systems from T7-infected Escherichia coli F- and F+ cells. J Virol. 1975 Dec;16(6):1483–1491. doi: 10.1128/jvi.16.6.1483-1491.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  149. Yokota T., Kanamaru Y., Mori R., Akiba T. Recombination between a thermosensitive kanamycin resistance factor and a nonthermosensitive multiple-drug resistant factor. J Bacteriol. 1969 Jun;98(3):863–873. doi: 10.1128/jb.98.3.863-873.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  150. 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]
  151. van Embden J. D., van Leeuwen W. J., Guinée P. A. Interference with propagation of typing bacteriophages by extrachromosomal elements in Salmonella typhimurium: bacteriophage type 505. J Bacteriol. 1976 Sep;127(3):1414–1426. doi: 10.1128/jb.127.3.1414-1426.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Microbiological Reviews are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES