Literature DB >> 6858000

Morphogenesis of filamentous bacteriophage f1: orientation of extrusion and production of polyphage.

J Lopez, R E Webster.   

Abstract

Crosslinking reagents were used to interrupt the process of filamentous phage morphogenesis and investigate the orientation in which nascent virions are extruded through the host cell membrane. Infected bacteria with emerging phage particles were crosslinked with glutaraldehyde. Immunoferritin-labeling studies on these emerging phage using anti-A protein IgG suggested that extrusion begins with the C protein end. To confirm this, phage extruding from infected bacteria were frozen using the reversible crosslinker dimethyl 3,3'-dithiobis-propionimidate and fragments of emerging phage were isolated by shearing. Protein analysis of these fragments showed them to be enriched in C protein relative to A protein, as predicted if phage extrusion begins with the C protein end. The production of multiple-length phage particles (polyphage) by nonpermissive bacterial hosts infected with amber mutant phage strains was also studied. Polyphage were produced upon infection with amber mutants in genes III, VI, VII, and IX which code for proteins found at the ends of the mature phage particle. No polyphage were produced by mutants in the other genes tested. Gene III amber mutants produce noninfective polyphage, but those produced by genes VII and IX are infective. Gene VI amber mutants appear to produce unstable, noninfective polyphage particles.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6858000     DOI: 10.1016/0042-6822(83)90382-3

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


  26 in total

1.  Structural characterization of ordered arrays of sn-glycerol-3-phosphate acyltransferase from Escherichia coli.

Authors:  W O Wilkison; R M Bell; K A Taylor; M J Costello
Journal:  J Bacteriol       Date:  1992-10       Impact factor: 3.490

2.  The level of expression of the minor pilin subunit, CooD, determines the number of CS1 pili assembled on the cell surface of Escherichia coli.

Authors:  H Sakellaris; V R Penumalli; J R Scott
Journal:  J Bacteriol       Date:  1999-03       Impact factor: 3.490

Review 3.  The basic structure of filamentous phage and its use in the display of combinatorial peptide libraries.

Authors:  S Cabilly
Journal:  Mol Biotechnol       Date:  1999-09       Impact factor: 2.695

4.  Membrane localization and topology of a viral assembly protein.

Authors:  J K Guy-Caffey; M P Rapoza; K A Jolley; R E Webster
Journal:  J Bacteriol       Date:  1992-04       Impact factor: 3.490

Review 5.  Ff coliphages: structural and functional relationships.

Authors:  I Rasched; E Oberer
Journal:  Microbiol Rev       Date:  1986-12

6.  fipB and fipC: two bacterial loci required for morphogenesis of the filamentous bacteriophage f1.

Authors:  J Lopez; R E Webster
Journal:  J Bacteriol       Date:  1985-09       Impact factor: 3.490

7.  Characterization of the cloned fip gene and its product.

Authors:  M Russel; P Model
Journal:  J Bacteriol       Date:  1984-02       Impact factor: 3.490

8.  Effects of bacteriophage fd infection on Escherichia coli HB11 envelope: a morphological and biochemical study.

Authors:  M E Bayer; M H Bayer
Journal:  J Virol       Date:  1986-01       Impact factor: 5.103

9.  pIIICTX, a predicted CTXphi minor coat protein, can expand the host range of coliphage fd to include Vibrio cholerae.

Authors:  Andrew J Heilpern; Matthew K Waldor
Journal:  J Bacteriol       Date:  2003-02       Impact factor: 3.490

Review 10.  Viruses: incredible nanomachines. New advances with filamentous phages.

Authors:  Marcus A Hemminga; Werner L Vos; Petr V Nazarov; Rob B M Koehorst; Cor J A M Wolfs; Ruud B Spruijt; David Stopar
Journal:  Eur Biophys J       Date:  2009-08-13       Impact factor: 1.733

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.