Literature DB >> 16562138

Episome-mediated Transfer of Drug Resistance in Enterobacteriaceae X. Restriction and Modification of Phages by fi R Factors.

T Watanabe1, T Takano, T Arai, H Nishida, S Sato.   

Abstract

Watanabe, Tsutomu (Keio University, Tokyo, Japan), Toshiya Takano, Toshihiko Arai, Hiroshi Nishida, and Sachiko Sato. Episome-mediated transfer of drug resistance in Enterobacteriaceae. X. Restriction and modification of phages by fi(-) R factors. J. Bacteriol. 92:477-486. 1966.-An fi(-) R factor, which restricts phages lambda, T1, and T7 without modifying them, was found to restrict and not to modify an F(-)-specific phage, W-31, in Escherichia coli K-12, but not to restrict phage P-22 in Salmonella typhimurium LT-2, whereas other fi(-) R factors restricted and modified P-22 but not W-31; fi(+) R factors did not restrict these phages. Transduction and lysogenization with phages lambda and P-22 were reduced by these fi(-) R factors in K-12 and LT-2, respectively, and the transducing phages lambda and P-22 were modified by these fi(-) R factors. Spontaneous as well as ultraviolet-induced production of phage P-22 and zygotic induction of phage lambda were not significantly affected by any R factor. Injection of the nucleic acids of phages T1 and lambda was not affected by R factors, but the injected phage nucleic acids were rapidly broken down in the bacteria carrying fi(-) R factors. The nucleic acids of the modified phages were not broken down in these bacteria. It was assumed from these results that the mechanism of restriction of phages by fi(-) R factors is due to the breakdown of the injected phage nucleic acids by a deoxyribonuclease(s), presumably located near the cell surface in the cells carrying fi(-) R factors. The deoxyribonuclease(s), formed in the cells carrying the nonmodifying fi(-) R factor, is considered to be different from that synthesized in the cells carrying the modifying fi(-) R factors. It was further shown that the average burst sizes of the unmodified as well as modified phages are slightly reduced by the presence of the fi(-) R factors.

Entities:  

Year:  1966        PMID: 16562138      PMCID: PMC276266          DOI: 10.1128/jb.92.2.477-486.1966

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  26 in total

1.  [Processes of conjugation and recombination in Escherichia coli. I. Induction by conjugation or zygotic induction].

Authors:  F JACOB; E L WOLLMAN
Journal:  Ann Inst Pasteur (Paris)       Date:  1956-10

2.  Localization of E. coli endonuclease I.

Authors:  C Cordonnier; G Bernardi
Journal:  Biochem Biophys Res Commun       Date:  1965-09-08       Impact factor: 3.575

Review 3.  The structure, function, synthesis and genetic control of bacterial pili and a molecular model for DNA and RNA transport in gram negative bacteria.

Authors:  C C Brinton
Journal:  Trans N Y Acad Sci       Date:  1965-06

Review 4.  Host-controlled modification of bacteriophage.

Authors:  W Arber
Journal:  Annu Rev Microbiol       Date:  1965       Impact factor: 15.500

5.  Reversal of restriction for host modified T2 and T4 DNA upon conversion of non-permissive Escherichia coli to spheroplasts.

Authors:  B Molholt; D Fraser
Journal:  Biochem Biophys Res Commun       Date:  1965-05-18       Impact factor: 3.575

6.  Effect of phage-controlled restriction on genetic linkage in bacterial crosses.

Authors:  J Pittard
Journal:  J Bacteriol       Date:  1964-05       Impact factor: 3.490

7.  The relation of resistance transfer factors to the F-factor (sex-factor) of Escherichia coli K12.

Authors:  E Meynell; N Datta
Journal:  Genet Res       Date:  1966-02       Impact factor: 1.588

8.  Functional homology of the sex-factor and resistance transfer factors.

Authors:  E Meynell; N Datta
Journal:  Nature       Date:  1965-08-21       Impact factor: 49.962

9.  Host-controlled restriction and modification of deoxyribonucleic acid in Escherichia coli.

Authors:  S Lederberg
Journal:  Virology       Date:  1965-11       Impact factor: 3.616

10.  Independent functions of viral protein and nucleic acid in growth of bacteriophage.

Authors:  A D HERSHEY; M CHASE
Journal:  J Gen Physiol       Date:  1952-05       Impact factor: 4.086

View more
  31 in total

1.  Endonuclease R-EcoRII restriction of bacteriophage f1 DNA in vitro: ordering of genes V and VII, location of an RNA promotor for gene VIII.

Authors:  G F Vovis; K Horiuchi; N D Zinder
Journal:  J Virol       Date:  1975-09       Impact factor: 5.103

2.  Inhibition of bacteriophage lambda, T1, and T7 development by R plasmids of the H incompatibility group.

Authors:  D E Taylor; R B Grant
Journal:  Antimicrob Agents Chemother       Date:  1976-10       Impact factor: 5.191

3.  Chromosomal regulation of sexual expression in Escherichia coli.

Authors:  T J Lerner; N D Zinder
Journal:  J Bacteriol       Date:  1979-02       Impact factor: 3.490

4.  Association of tellurium resistance and bacteriophage inhibition conferred by R plasmids.

Authors:  D E Taylor; A O Summers
Journal:  J Bacteriol       Date:  1979-03       Impact factor: 3.490

5.  R plasmids of the S incompatibility group belong to the H2 incompatibility group.

Authors:  D E Taylor; R B Grant
Journal:  Antimicrob Agents Chemother       Date:  1977-09       Impact factor: 5.191

6.  Incompatibility and bacteriophage inhibition properties of N-1, a plasmid belonging to the H2 incompatibility group.

Authors:  D E Taylor; R B Grant
Journal:  Mol Gen Genet       Date:  1977-05-20

7.  Inhibition of transformation and transfection in Haemophilus influenzae Rd9 by lysogeny.

Authors:  A Piekarowicz; M Siwińska
Journal:  J Bacteriol       Date:  1977-01       Impact factor: 3.490

8.  Methylation of cytosine residues in DNA controlled by a drug resistance factor (host-induced modification-R factors-N 6 -methyladenine-5-methylcytosine).

Authors:  S Hattman; E Gold; A Plotnik
Journal:  Proc Natl Acad Sci U S A       Date:  1972-01       Impact factor: 11.205

9.  Plasmid control of recombination of E. coli K12.

Authors:  L S Chernin; M I Ovadis
Journal:  Mol Gen Genet       Date:  1980

10.  Variation of 6-methylaminopurine content in bacteriophage P22 deoxyribonucleic acid as a function of host specificity.

Authors:  S Hattman
Journal:  J Virol       Date:  1971-05       Impact factor: 5.103

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