Literature DB >> 6234699

Multiple factors and processes involved in host cell killing by bacteriophage Mu: characterization and mapping.

B T Waggoner, C F Marrs, M M Howe, M L Pato.   

Abstract

The regions of bacteriophage Mu involved in host cell killing were determined by infection of a lambda-immune host with 12 lambda pMu-transducing phages carrying different amounts of Mu DNA beginning at the left end. Infecting lambda pMu phages containing 5.0 (+/- 0.2) kb or less of the left end of Mu DNA did not kill the lambda-immune host, whereas lambda pMu containing 5.1 kb did kill, thus locating the right end of the kil gene between approximately 5.0 and 5.1 kb. For the Kil+ phages the extent of killing increased as the multiplicity of infection (m.o.i.) increased. In addition, killing was also affected by the presence of at least two other regions of Mu DNA: one, located between 5.1 and 5.8 kb, decreased the extent of killing; the other, located between 6.3 and 7.9 kb, greatly increased host cell killing. Killing was also assayed after lambda pMu infection of a lambda-immune host carrying a mini-Mu deleted for most of the B gene and the middle region of Mu DNA. Complementation of mini-Mu replication by infecting B+ lambda pMu phages resulted in killing of the lambda-immune, mini-Mu-containing host, regardless of the presence or absence of the Mu kil gene. The extent of host cell killing increased as the m.o.i. of the infecting lambda pMu increased, and was further enhanced by both the presence of the kil gene and the region located between 6.3 and 7.9 kb. These distinct processes of kil-mediated killing in the absence of replication and non-kil-mediated killing in the presence of replication were also observed after induction of replication-deficient and kil mutant prophages, respectively.

Entities:  

Mesh:

Substances:

Year:  1984        PMID: 6234699     DOI: 10.1016/0042-6822(84)90257-5

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  8 in total

1.  Synchronous division induced in Escherichia coli K12 by gemts mutants of phage Mu.

Authors:  L Paolozzi; A Nicosia; J C Liebart; P Ghelardini
Journal:  Mol Gen Genet       Date:  1989-07

2.  Mini-Mu transposition of bacterial genes on the transmissible plasmid.

Authors:  M Weiserová; J Hubácek; V Brenner; E S Piruzian; N S Kobec; G A Velikodvorskaya
Journal:  Folia Microbiol (Praha)       Date:  1987       Impact factor: 2.099

3.  Characterization of Mu prophage lacking the central strong gyrase binding site: localization of the block in replication.

Authors:  M L Pato; M Karlok; C Wall; N P Higgins
Journal:  J Bacteriol       Date:  1995-10       Impact factor: 3.490

4.  In vivo mutagenesis of bacteriophage Mu transposase.

Authors:  A Toussaint; L Desmet; M Faelen; R Alazard; M Chandler; M Pato
Journal:  J Bacteriol       Date:  1987-12       Impact factor: 3.490

5.  Mutants of Escherichia coli defective for replicative transposition of bacteriophage Mu.

Authors:  W Ross; S H Shore; M M Howe
Journal:  J Bacteriol       Date:  1986-09       Impact factor: 3.490

6.  Inhibition of bacterial segregation by early functions of phage mu and association of replication protein B with the inner cell membrane.

Authors:  C Boeckh; E G Bade; H Delius; J N Reeve
Journal:  Mol Gen Genet       Date:  1986-03

7.  Lysogenization of Escherichia coli him+, himA, and himD hosts by bacteriophage Mu.

Authors:  R B Bourret; M S Fox
Journal:  J Bacteriol       Date:  1988-04       Impact factor: 3.490

8.  Neighboring plasmid sequences can affect Mini-Mu DNA transposition in the absence of expression of the bacteriophage Mu semi-essential early region.

Authors:  J Harel; M S DuBow
Journal:  Arch Microbiol       Date:  1994       Impact factor: 2.552

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.