Literature DB >> 8509344

Phi X174 E complements lambda S and R dysfunction for host cell lysis.

W D Roof1, R Young.   

Abstract

Hybrid lambda phages which have the E lysis gene of the bacteriophage phi X174 in cis to defective nonsense and deletion alleles of the normal lambda lysis genes S and R have been constructed and shown to be fully competent for plaque-forming ability, which demonstrates that the single-gene, lysozyme-independent lysis system of phi X174 and related phages can serve the lytic function for large complex phages. These hybrid phages are unable to form plaques on a slyD host. Moreover, plaque morphology indicates that in E-mediated lysis the soluble lambda R endolysin can participate in lysis, indicating that the protein E-mediated lesions are not completely sealed off from the periplasm.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8509344      PMCID: PMC204810          DOI: 10.1128/jb.175.12.3909-3912.1993

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


  17 in total

Review 1.  Bacteriophage lysis: mechanism and regulation.

Authors:  R Young
Journal:  Microbiol Rev       Date:  1992-09

2.  KINETICS OF BACTERIOPHAGE RELEASE BY SINGLE CELLS OF PHI X174-INFECTED E. COLI.

Authors:  C A HUTCHISON; R L SINSHEIMER
Journal:  J Mol Biol       Date:  1963-08       Impact factor: 5.469

3.  Endogenous transmembrane tunnel formation mediated by phi X174 lysis protein E.

Authors:  A Witte; G Wanner; U Bläsi; G Halfmann; M Szostak; W Lubitz
Journal:  J Bacteriol       Date:  1990-07       Impact factor: 3.490

4.  Phi X174 protein E-mediated lysis of Escherichia coli.

Authors:  A Witte; U Bläsi; G Halfmann; M Szostak; G Wanner; W Lubitz
Journal:  Biochimie       Date:  1990 Feb-Mar       Impact factor: 4.079

5.  Proton-motive-force-dependent step in the pathway to lysis of Escherichia coli induced by bacteriophage phi X174 gene E product.

Authors:  A Witte; W Lubitz; E P Bakker
Journal:  J Bacteriol       Date:  1987-04       Impact factor: 3.490

6.  Dominance in lambda S mutations and evidence for translational control.

Authors:  R Raab; G Neal; C Sohaskey; J Smith; R Young
Journal:  J Mol Biol       Date:  1988-01-05       Impact factor: 5.469

7.  Nucleotide sequence of bacteriophage lambda DNA.

Authors:  F Sanger; A R Coulson; G F Hong; D F Hill; G B Petersen
Journal:  J Mol Biol       Date:  1982-12-25       Impact factor: 5.469

8.  The process of infection with bacteriophage phi-X174. X. Mutations in a phi-X Lysis gene.

Authors:  C A Hutchison; R L Sinsheimer
Journal:  J Mol Biol       Date:  1966-07       Impact factor: 5.469

9.  The lethal lambda S gene encodes its own inhibitor.

Authors:  U Bläsi; C Y Chang; M T Zagotta; K B Nam; R Young
Journal:  EMBO J       Date:  1990-04       Impact factor: 11.598

10.  Lysis of Escherichia coli by cloned phi X174 gene E depends on its expression.

Authors:  U Bläsi; B Henrich; W Lubitz
Journal:  J Gen Microbiol       Date:  1985-05
View more
  4 in total

1.  Genetic evidence that the bacteriophage phi X174 lysis protein inhibits cell wall synthesis.

Authors:  T G Bernhardt; W D Roof; R Young
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-11       Impact factor: 11.205

Review 2.  Phage lysis: do we have the hole story yet?

Authors:  Ry Young
Journal:  Curr Opin Microbiol       Date:  2013-10-08       Impact factor: 7.934

3.  Functions involved in bacteriophage P2-induced host cell lysis and identification of a new tail gene.

Authors:  R Ziermann; B Bartlett; R Calendar; G E Christie
Journal:  J Bacteriol       Date:  1994-08       Impact factor: 3.490

4.  A Titratable Cell Lysis-on-Demand System for Droplet-Compartmentalized Ultrahigh-Throughput Screening in Functional Metagenomics and Directed Evolution.

Authors:  Che Fai Alex Wong; Liisa van Vliet; Swapnil Vilas Bhujbal; Chengzhi Guo; Marit Sletmoen; Bjørn Torger Stokke; Florian Hollfelder; Rahmi Lale
Journal:  ACS Synth Biol       Date:  2021-07-14       Impact factor: 5.110

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.