Literature DB >> 6540006

Phosphate repression of phage protein synthesis during infection by choleraphage phi 149.

P Ray, A Sengupta, J Das.   

Abstract

A synthetic medium for choleraphage phi 149 growth, in which the concentration of phosphate ions plays a significant role, has been defined. Upon infection, choleraphage phi 149 DNA binds to the cell membrane at three to four sites. The host macromolecular syntheses are shut off by 10 min after infection and the synthesis of phage-specific DNA is detectable after 20 min of infection. The phage utilizes primarily the host DNA degradation products for its own DNA synthesis. When added during the first 20 min of infection both nalidixic acid and novobiocin inhibit phage growth. The effects of these antibiotics are not pronounced when added late during infection. Pulse labeling of ultraviolet-irradiated infected cells at different times during infection has allowed identification of about 50 phage-specific proteins of which 19 are structural proteins. These proteins appear during the infection cycle in two distinct phases, early and late. When infection is carried out in high-phosphate medium, none of the late proteins is synthesized. Eleven of the 26 early proteins detected are DNA-binding proteins.

Entities:  

Mesh:

Substances:

Year:  1984        PMID: 6540006     DOI: 10.1016/0042-6822(84)90252-6

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


  9 in total

1.  Replication and packaging of choleraphage phi 149 DNA.

Authors:  R Chowdhury; A Ray; P Ray; J Das
Journal:  J Virol       Date:  1987-12       Impact factor: 5.103

Review 2.  Genetics of Vibrio cholerae and its bacteriophages.

Authors:  A Guidolin; P A Manning
Journal:  Microbiol Rev       Date:  1987-06

3.  Infection by choleraphage phi 138: bacteriophage DNA and replicative intermediates.

Authors:  R Chowdhury; J Das
Journal:  J Virol       Date:  1986-03       Impact factor: 5.103

4.  Abortive replication of choleraphage phi 149 in Vibrio cholerae biotype el tor.

Authors:  R Chowdhury; S K Biswas; J Das
Journal:  J Virol       Date:  1989-01       Impact factor: 5.103

5.  Cloning and expression in Escherichia coli of a recA-like gene from Vibrio cholerae.

Authors:  K Paul; S K Ghosh; J Das
Journal:  Mol Gen Genet       Date:  1986-04

6.  Cloning and characterization of mutL and mutS genes of Vibrio cholerae: nucleotide sequence of the mutL gene.

Authors:  T K Bera; S K Ghosh; J Das
Journal:  Nucleic Acids Res       Date:  1989-08-11       Impact factor: 16.971

7.  Heat shock response and heat shock protein antigens of Vibrio cholerae.

Authors:  G K Sahu; R Chowdhury; J Das
Journal:  Infect Immun       Date:  1994-12       Impact factor: 3.441

8.  A 14-kilodalton inner membrane protein of Vibrio cholerae biotype e1 tor confers resistance to group IV choleraphage infection to classical vibrios.

Authors:  S K Biswas; R Chowdhury; J Das
Journal:  J Bacteriol       Date:  1992-10       Impact factor: 3.490

9.  Cell surface characteristics of environmental and clinical isolates of Vibrio cholerae non-O1.

Authors:  K Chaudhuri; R K Bhadra; J Das
Journal:  Appl Environ Microbiol       Date:  1992-11       Impact factor: 4.792

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.