Literature DB >> 2981800

Release of respiratory control in Escherichia coli after bacteriophage adsorption: process independent of DNA injection.

L Letellier, B Labedan.   

Abstract

Adsorption of phages T4, T5, and BF23 to previously starved Escherichia coli cells triggered the immediate release of respiratory control. A similar stimulation of respiration was induced after T4 ghost attachment, showing that this process was independent of the mechanism of DNA injection. Rather, this change in the respiratory rate was related to the transient depolarization of the cytoplasmic membrane also induced after phage and ghost adsorption. Both processes were suppressed by addition of ethylene glycol-bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid in the case of T4 (phage and ghosts) but not of T5 and BF23. The increase in respiratory rate observed after phage adsorption was of a magnitude similar to that induced by protonophores. Since other treatments that depolarize the membrane without a massive proton influx did not increase the rate of respiration of starved bacteria with the same efficiency, these results suggest that phage adsorption induced an entry of protons into the cell cytoplasm.

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Year:  1985        PMID: 2981800      PMCID: PMC214853          DOI: 10.1128/jb.161.1.179-182.1985

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


  16 in total

1.  The role of energy-yielding ATPase and respiratory chain at early stages of bacteriophage T4 infection.

Authors:  E Kalasauskaite; L Grinius
Journal:  FEBS Lett       Date:  1979-03-15       Impact factor: 4.124

2.  Proton electrochemical gradient in Escherichia coli cells and its relation to active transport of lactose.

Authors:  D Zilberstein; S Schuldiner; E Padan
Journal:  Biochemistry       Date:  1979-02-20       Impact factor: 3.162

3.  Respiratory control in Escherichia coli K 12.

Authors:  C Burstein; L Tiankova; A Kepes
Journal:  Eur J Biochem       Date:  1979-03

4.  Evidence for heterogeneity in populations of T5 bacteriophage.

Authors:  B Labedan; J Legault-Demare
Journal:  J Virol       Date:  1974-05       Impact factor: 5.103

5.  Requirement for membrane potential in injection of phage T4 DNA.

Authors:  B Labedan; E B Goldberg
Journal:  Proc Natl Acad Sci U S A       Date:  1979-09       Impact factor: 11.205

6.  Membrane potential changes during the first steps of coliphage infection.

Authors:  B Labedan; L Letellier
Journal:  Proc Natl Acad Sci U S A       Date:  1981-01       Impact factor: 11.205

7.  Probes of membrane potential in Escherichia coli cells.

Authors:  A Ghazi; E Schechter; L Letellier; B Labedan
Journal:  FEBS Lett       Date:  1981-03-23       Impact factor: 4.124

8.  A membrane potential threshold for phage T4 DNA injection.

Authors:  B Labedan; K B Heller; A A Jasaitis; T H Wilson; E B Goldberg
Journal:  Biochem Biophys Res Commun       Date:  1980-03-28       Impact factor: 3.575

9.  Cyanine dye as monitor of membrane potentials in Escherichia coli cells and membrane vesicles.

Authors:  L Letellier; E Shechter
Journal:  Eur J Biochem       Date:  1979-12-17

10.  Metabolism of T4 bacteriophage ghost-infected cells: effect of bacteriophage and ghosts on the uptake of carbohydrates in Escherichia coli B.

Authors:  H H Winkler; D H Duckworth
Journal:  J Bacteriol       Date:  1971-07       Impact factor: 3.490

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  3 in total

1.  Genetic response to bacteriophage infection in Lactococcus lactis reveals a four-strand approach involving induction of membrane stress proteins, D-alanylation of the cell wall, maintenance of proton motive force, and energy conservation.

Authors:  Vincenzo Fallico; R Paul Ross; Gerald F Fitzgerald; Olivia McAuliffe
Journal:  J Virol       Date:  2011-08-31       Impact factor: 5.103

2.  Involvement of host cell energy in the transfection of Lactobacillus casei protoplasts with phage PL-1 DNA.

Authors:  K Watanabe; Y Kakita; Y Nakashima; F Miake
Journal:  Curr Microbiol       Date:  1995-01       Impact factor: 2.188

3.  Contact-dependent growth inhibition causes reversible metabolic downregulation in Escherichia coli.

Authors:  S K Aoki; J S Webb; B A Braaten; D A Low
Journal:  J Bacteriol       Date:  2009-01-05       Impact factor: 3.490

  3 in total

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