Literature DB >> 8416903

Host RecJ is required for growth of P22 erf bacteriophage.

M J Mahan1, A Garzón, J Casadesús.   

Abstract

Growth of bacteriophage P22 erf is known to require host RecA recombination function. We show that the RecA function is necessary but not sufficient to restore the plaque-forming ability of phage P22 erf; such mutant phage also requires host RecJ function. The residual efficiency of plaquing of P22 erf in a recJ background (0.03%) is completely abolished in recJ recB hosts (< 0.001%), suggesting that the RecBCD nuclease can provide an alternative function allowing phage growth. One tentative explanation is that circularization of P22 erf DNA mostly proceeds through the RecF pathway of recombination; however, less efficient circularization via the RecBCD pathway may also occur. In a recJ background, lysates obtained upon induction of an erf prophage show reduced yield (10%), suggesting that growth of P22 erf may require host RecJ in a step(s) other than circularization of phage DNA.

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Year:  1993        PMID: 8416903      PMCID: PMC196124          DOI: 10.1128/jb.175.1.288-290.1993

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


  18 in total

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Authors:  M J Mahan; J R Roth
Journal:  J Bacteriol       Date:  1989-01       Impact factor: 3.490

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Authors:  S T Lovett; A J Clark
Journal:  J Bacteriol       Date:  1985-04       Impact factor: 3.490

3.  Modulation of Escherichia coli RecBCD activity by the bacteriophage lambda Gam and P22 Abc functions.

Authors:  A R Poteete; A C Fenton; K C Murphy
Journal:  J Bacteriol       Date:  1988-05       Impact factor: 3.490

Review 4.  Molecular genetics of bacteriophage P22.

Authors:  M M Susskind; D Botstein
Journal:  Microbiol Rev       Date:  1978-06

5.  Contribution of the bacterial recombination function to replication of bacteriophage P2.

Authors:  H Yamagami; N Yamamoto
Journal:  J Mol Biol       Date:  1970-10-28       Impact factor: 5.469

6.  recA-independent general genetic recombination of plasmids.

Authors:  R A Fishel; A A James; R Kolodner
Journal:  Nature       Date:  1981-11-12       Impact factor: 49.962

7.  his operons of Escherichia coli and Salmonella typhimurium are regulated by DNA supercoiling.

Authors:  K E Rudd; R Menzel
Journal:  Proc Natl Acad Sci U S A       Date:  1987-01       Impact factor: 11.205

8.  Genetic recombination of bacterial plasmid DNA: effect of RecF pathway mutations on plasmid recombination in Escherichia coli.

Authors:  R Kolodner; R A Fishel; M Howard
Journal:  J Bacteriol       Date:  1985-09       Impact factor: 3.490

9.  Isolation of genetic elements that increase frequencies of plasmid recombinants.

Authors:  A A James; P T Morrison; R Kolodner
Journal:  Nature       Date:  1983 May 19-25       Impact factor: 49.962

10.  Interplasmidic and intraplasmidic recombination in Escherichia coli K-12.

Authors:  A Laban; A Cohen
Journal:  Mol Gen Genet       Date:  1981
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  3 in total

1.  recB recJ mutants of Salmonella typhimurium are deficient in transductional recombination, DNA repair and plasmid maintenance.

Authors:  A Garzón; C R Beuzón; M J Mahan; J Casadesús
Journal:  Mol Gen Genet       Date:  1996-03-20

Review 2.  Genetic map of Salmonella typhimurium, edition VIII.

Authors:  K E Sanderson; A Hessel; K E Rudd
Journal:  Microbiol Rev       Date:  1995-06

3.  Sak and Sak4 recombinases are required for bacteriophage replication in Staphylococcus aureus.

Authors:  Maan M Neamah; Ignacio Mir-Sanchis; María López-Sanz; Sonia Acosta; Ignacio Baquedano; Andreas F Haag; Alberto Marina; Silvia Ayora; José R Penadés
Journal:  Nucleic Acids Res       Date:  2017-06-20       Impact factor: 16.971

  3 in total

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