Literature DB >> 3001021

fii, a bacterial locus required for filamentous phage infection and its relation to colicin-tolerant tolA and tolB.

T P Sun, R E Webster.   

Abstract

We describe mutations in a new bacterial locus, designated fii, which do not allow the filamentous bacteriophage f1 to infect bacteria harboring the F plasmid. Mutations at this locus do not affect the ability of F plasmid-containing bacteria to undergo conjugation or be infected by the F plasmid-specific RNA phage f2. The filamentous phage can still adsorb to the F sex pilus, but the DNA is unable to enter the bacteria. All fii mutants become tolerant to colicins E1, E2, and E3. Strains with amber mutations in fii also are unable to plaque P1, even though they can be infected with this phage. Mutations in fii also prevent infection of bacteria harboring the N plasmid by the filamentous bacteriophage IKe. The fii locus maps adjacent to tolA, mutants of which demonstrate tolerance to high levels of the E and K colicins. The three genes tolA, tolB, and fii are shown to reside on a 4.3-kilobase fragment of the Escherichia coli chromosome. Each gene has been cloned into a chimeric plasmid and shown to complement, in trans, mutations at the corresponding chromosomal locus. Studies in maxicells show that the product of fii appears to be a 24-kilodalton protein which copurifies with the cell envelope. The product of tolA has been identified tentatively as a 51-kilodalton protein. Data from cloning, Tn5 mutagenesis, and P1 transduction studies are consistent with the gene order sucA-fii-tolA-tolB-aroG near 17 min on the E. coli map.

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Year:  1986        PMID: 3001021      PMCID: PMC214377          DOI: 10.1128/jb.165.1.107-115.1986

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


  45 in total

1.  Mutagenesis by insertion of a drug-resistance element carrying an inverted repetition.

Authors:  N Kleckner; R K Chan; B K Tye; D Botstein
Journal:  J Mol Biol       Date:  1975-10-05       Impact factor: 5.469

2.  Binding, eclipse, and penetration of the filamentous bacteriophage M13 in intact and disrupted cells.

Authors:  R Marco; S M Jazwinski; A Kornberg
Journal:  Virology       Date:  1974-11       Impact factor: 3.616

3.  Resistance to colicins E3 and K induced by infection with bacteriophage f1.

Authors:  N D Zinder
Journal:  Proc Natl Acad Sci U S A       Date:  1973-11       Impact factor: 11.205

4.  Role of F pili in the penetration of bacteriophage fl.

Authors:  A Jacobson
Journal:  J Virol       Date:  1972-10       Impact factor: 5.103

Review 5.  Bacterial conjugation.

Authors:  R Curtiss
Journal:  Annu Rev Microbiol       Date:  1969       Impact factor: 15.500

6.  A simple method for DNA restriction site mapping.

Authors:  H O Smith; M L Birnstiel
Journal:  Nucleic Acids Res       Date:  1976-09       Impact factor: 16.971

7.  Transport of vitamin B12 in Escherichia coli: common receptor sites for vitamin B12 and the E colicins on the outer membrane of the cell envelope.

Authors:  D R Di Masi; J C White; C A Schnaitman; C Bradbeer
Journal:  J Bacteriol       Date:  1973-08       Impact factor: 3.490

8.  Transport of vitamin B12 in Escherichia coli: genetic studies.

Authors:  R J Kadner; G L Liggins
Journal:  J Bacteriol       Date:  1973-08       Impact factor: 3.490

9.  Bacteriophage f1 infection: fate of the parental major coat protein.

Authors:  H Smilowitz
Journal:  J Virol       Date:  1974-01       Impact factor: 5.103

10.  Bacteriophage f1 infection and colicin tolerance.

Authors:  H Smilowitz
Journal:  J Virol       Date:  1974-01       Impact factor: 5.103

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  64 in total

1.  Role of TolR N-terminal, central, and C-terminal domains in dimerization and interaction with TolA and tolQ.

Authors:  L Journet; A Rigal; C Lazdunski; H Bénédetti
Journal:  J Bacteriol       Date:  1999-08       Impact factor: 3.490

2.  The phage infection process: a functional role for the distal linker region of bacteriophage protein 3.

Authors:  N Nilsson; A C Malmborg; C A Borrebaeck
Journal:  J Virol       Date:  2000-05       Impact factor: 5.103

3.  TonB interacts with nonreceptor proteins in the outer membrane of Escherichia coli.

Authors:  Penelope I Higgs; Tracy E Letain; Kelley K Merriam; Neal S Burke; HaJeung Park; ChulHee Kang; Kathleen Postle
Journal:  J Bacteriol       Date:  2002-03       Impact factor: 3.490

4.  In vivo synthesis of the periplasmic domain of TonB inhibits transport through the FecA and FhuA iron siderophore transporters of Escherichia coli.

Authors:  S P Howard; C Herrmann; C W Stratilo; V Braun
Journal:  J Bacteriol       Date:  2001-10       Impact factor: 3.490

5.  The mechanism of bacterial infection by filamentous phages involves molecular interactions between TolA and phage protein 3 domains.

Authors:  Fredrik Karlsson; Carl A K Borrebaeck; Nina Nilsson; Ann-Christin Malmborg-Hager
Journal:  J Bacteriol       Date:  2003-04       Impact factor: 3.490

Review 6.  Molecular interaction between bacteriophage and the gram-negative cell envelope.

Authors:  K J Heller
Journal:  Arch Microbiol       Date:  1992       Impact factor: 2.552

7.  Localization and assembly into the Escherichia coli envelope of a protein required for entry of colicin A.

Authors:  J P Bourdineaud; S P Howard; C Lazdunski
Journal:  J Bacteriol       Date:  1989-05       Impact factor: 3.490

8.  Interactions of the energy transducer TonB with noncognate energy-harvesting complexes.

Authors:  Kerry K Brinkman; Ray A Larsen
Journal:  J Bacteriol       Date:  2007-10-26       Impact factor: 3.490

9.  Structure of the periplasmic domain of Pseudomonas aeruginosa TolA: evidence for an evolutionary relationship with the TonB transporter protein.

Authors:  Michael Witty; Carolina Sanz; Amish Shah; J Günter Grossmann; Kenji Mizuguchi; Richard N Perham; Ben Luisi
Journal:  EMBO J       Date:  2002-08-15       Impact factor: 11.598

10.  pIIICTX, a predicted CTXphi minor coat protein, can expand the host range of coliphage fd to include Vibrio cholerae.

Authors:  Andrew J Heilpern; Matthew K Waldor
Journal:  J Bacteriol       Date:  2003-02       Impact factor: 3.490

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