Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Microbiology 145 (1999), 1649-1659
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Chua, J.
Right arrow Articles by Morona, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chua, J.
Right arrow Articles by Morona, R.
Agricola
Right arrow Articles by Chua, J.
Right arrow Articles by Morona, R.

Microbiology, Vol 145, 1649-1659, Copyright © 1999 by Society for General Microbiology


ARTICLES

The Shigella flexneri bacteriophage Sf6 tailspike protein (TSP)/endorhamnosidase is related to the bacteriophage P22 TSP and has a motif common to exo- and endoglycanases, and C-5 epimerases

JEH Chua, PA Manning and R Morona
Department of Microbiology and Immunology, University of Adelaide, Adelaide, South Australia, Australia 5005

The temperate bacteriophage Sf6 infects Shigella flexneri strains of serotype X or Y, converting them into serotypes 3a or 3b, respectively. The tailspike protein (TSP) of Sf6 possesses endo-1,3-alpha-L-rhamnosidase (endorhamnosidase) activity which results in cleavage of the lipopolysaccharide O-antigen receptor during the adsorption of the phage to the cell surface. When used in Southern hybridization, a P22 gene 9 (encoding P22 TSP) DNA probe hybridized with restriction fragment PstI-7 of Sf6. DNA sequencing and analysis of PstI-7 and the adjacent PstI-8 fragment revealed an open reading frame (ORF1) of 1872 bp (624 amino acids) bearing amino acid sequence homology to the bacteriophage P22 TSP N-terminal head-binding domain. High conservation of key residues was suggestive of similar secondary and tertiary N-terminal protein structure and a similar function of the Sf6 TSP in this region. In addition, an amino acid sequence motif (DFGX(3)DGX(6)AX(3)A) was identified between residues 164 and 184 which was also found to exist in various prokaryotic and eukaryotic exo-/endoglycanases, C-5 epimerases and bacteriophage proteins. Expression of ORF1 from a T7 promoter produced a 67 kDa protein (detected by L-[35S]methionine labelling and SDS-PAGE). Assay of heat-treated cytoplasmic extracts containing the ORF1-encoded protein by incubation with whole Sh. flexneri Y cells demonstrated that O-antigen hydrolysis activity was present; ORF1 therefore encodes Sf6 TSP. Sf6 TSP exhibited specific and preferential activity for long-chain Sh. flexneri serotype X or Y O-antigen, cleavage of which resulted in the release of oligosaccharide fragments, consistent with octasaccharides in size, as detected by fluorophore-assisted carbohydrate electrophoresis (FACE).


This article has been cited by other articles:


Home page
J. Bacteriol.Home page
D. Scholl and C. Merril
The Genome of Bacteriophage K1F, a T7-Like Phage That Has Acquired the Ability To Replicate on K1 Strains of Escherichia coli
J. Bacteriol., December 15, 2005; 187(24): 8499 - 8503.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. Freiberg, R. Morona, L. Van Den Bosch, C. Jung, J. Behlke, N. Carlin, R. Seckler, and U. Baxa
The Tailspike Protein of Shigella Phage Sf6. A STRUCTURAL HOMOLOG OF SALMONELLA PHAGE P22 TAILSPIKE PROTEIN WITHOUT SEQUENCE SIMILARITY IN THE beta -HELIX DOMAIN
J. Biol. Chem., January 10, 2003; 278(3): 1542 - 1548.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
T. Barbeyron, G. Michel, P. Potin, B. Henrissat, and B. Kloareg
iota -Carrageenases Constitute a Novel Family of Glycoside Hydrolases, Unrelated to That of kappa -Carrageenases
J. Biol. Chem., November 3, 2000; 275(45): 35499 - 35505.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1999 Society for General Microbiology.