Home LiteratureArticle Details
PMID: 1104892 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

F-Factor-mediated restriction of bacteriophage T7: protein synthesis in cell-free systems from T7-infected Escherichia coli F- and F+ cells.

Journal of virology ·Vol. 16 ·No. 6 ·1975-12-00 ·Pages 1483-91

Yamada Y, Nakada D

Abstract

A characteristic phenomenon in the F-factor-mediated inhibition of T7 phage is a virtual absence of T7 late protein synthesis in T7-infected Escherichia coli male cells, in spite of the presence of T7 late mRNA which is translatable in vitro when isolated from the cell. To determine whether the translational defect in T7-infected F+ cells is due to a T7 late mRNA-specific translational block, or to a general decrease of F+ cell translational activity, we compared the activities of cell-free, protein-synthesizing systems prepared from isogenic F- and F+ cells harvested at different times of T7 infection. The cell-free systems from uninfected F- and F+ cells translated T7late mRNA equally as well as MS2 RNA and T7early mRNA. The activity of cell-free systems from T7-infected F+ cells to translate MS2 RAN, T7 early mRNA, and T7 late mRNA decreased concomitantly at a much faster rate than that of T7-infected F- cells. Therefore, the abortive infection of F+ cells by T7 does not result from a T7 late mRNA-specific translational inhibition, although a general reduction of the translational activity appears to be a major factor for the inability of the F+ cells to produce a sufficient amount of T7 late proteins.

MeSH Terms
Cell-Free System Coliphages/enzymology,growth & development,metabolism Conjugation, Genetic DNA-Directed RNA Polymerases/biosynthesis Escherichia coli/metabolism F Factor Muramidase/biosynthesis Mutation Protein Biosynthesis RNA, Messenger/metabolism RNA, Viral/metabolism Time Factors Viral Proteins/biosynthesis Virus Replication
Chemicals
RNA, Messenger RNA, Viral Viral Proteins DNA-Directed RNA Polymerases Muramidase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Yamada Y
Nakada D
References (10)
10 references, click to expand
  1. Early to late switch in bacteriophage T7 development: functional decay of T7 early messenger RNA.
    J Mol Biol. 1974 Oct 25;89(2):293-303 PMID: 4613858
  2. Functional instability of T7 early mRNA.
    Nature. 1974 Mar 22;248(446):335-8 PMID: 4594697
  3. T7 protein synthesis in F' episome-containing cells: assignment of specific proteins to three translational groups.
    J Virol. 1974 Feb;13(2):386-93 PMID: 4589855
  4. T7 translational control mechanisms and their inhibiton by F factors.
    Nat New Biol. 1971 May 12;231(19):37-41 PMID: 5283385
  5. F-Factor-mediated restriction of bacteriophage T7: synthesis of RNA and protein in T7-infected Escherichia coli F- and F+ cells.
    J Virol. 1975 Dec;16(6):1380-90 PMID: 1104891
  6. Evidence for the presence of nontranslated T7 late mRNA in infected F'(PIF+) episome-containing cells.
    J Virol. 1974 Feb;13(2):378-85 PMID: 4589854
  7. Bacteriophage T4 DNA-dependent in vitro synthesis of lysozyme.
    Proc Natl Acad Sci U S A. 1969 Aug;63(4):1351-8 PMID: 4901474
  8. Permeability lesions in male Escherichia coli infected with bacteriophage T7.
    Proc Natl Acad Sci U S A. 1975 Jun;72(6):2222-6 PMID: 1094459
  9. Cleavage of structural proteins during the assembly of the head of bacteriophage T4.
    Nature. 1970 Aug 15;227(5259):680-5 PMID: 5432063
  10. Translational control of bacteriophage MS2 RNA cistrons by MS2 coat protein: polyacrylamide gel electrophoretic analysis of proteins synthesized in vitro.
    J Mol Biol. 1968 Feb 14;31(3):431-40 PMID: 5637198
Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1975-12-00
Pages
1483-91
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC355757
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]