Literature DB >> 2116761

The bacteriophage kh receptor of Lactococcus lactis subsp. cremoris KH is the rhamnose of the extracellular wall polysaccharide.

R Valyasevi1, W E Sandine, B L Geller.   

Abstract

A receptor for bacteriophages of lactic acid bacteria, including Lactococcus lactis subsp. cremoris KH, was found on the cell wall and not on the cell membrane, as determined by a phage-binding assay of sodium dodecyl sulfate- and mutanolysin-treated cell walls. The cell wall carbohydrates of L. lactis subsp. cremoris KH were analyzed by gas chromatography and mass spectrometry and found to contain rhamnose, galactose, glucose and N-acetylglucosamine. Similar analysis of mutants that were reduced in the ability to bind phages kh, 643, c2, ml3, and 1 indicated that galactose was essential for binding all phages. In addition, rhamnose was required for binding phages kh and ml3. Inhibition studies of phage binding by using two different lectins with a specificity for galactose indicated that phage kh may not bind directly to galactose. Rather, galactose may be an essential structural component located in the vicinity of the receptor. Incubation of any of the five phages with rhamnose or of phage kh with purified cell walls inactivated the phages. Inactivation required divalent cations and was irreversible. Inactivation of phages was stereospecific for rhamnose, as neither L-(+)- nor D-(-)-fucose (the stereoisomers of rhamnose) inhibited the phage. Furthermore, phage infection of a culture was completely inhibited by the addition of rhamnose to the medium. Therefore, the receptor for phage kh appears to be a rhamnose component of the extracellular wall polysaccharide.

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Year:  1990        PMID: 2116761      PMCID: PMC184526          DOI: 10.1128/aem.56.6.1882-1889.1990

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  29 in total

1.  The adsorption of bacteriophage phi-X174 to its host.

Authors:  R FUJIMURA; P KAESBERG
Journal:  Biophys J       Date:  1962-11       Impact factor: 4.033

2.  Mechanism of adsorption and eclipse of bacteriophage phi chi 174. 3. Comparison of the activation parameters for the in vitro and in vivo eclipse reactions with mutant and wild-type virus.

Authors:  N L Incardona
Journal:  J Virol       Date:  1974-09       Impact factor: 5.103

3.  Isolation and properties of a phage receptor substance from the plasma membrane of Streptococcus lactis ML 3.

Authors:  J D Oram
Journal:  J Gen Virol       Date:  1971-10       Impact factor: 3.891

4.  The kinetics of reversible and irreversible attachment of bacteriophage T-1.

Authors:  J R Christensen
Journal:  Virology       Date:  1965-08       Impact factor: 3.616

5.  Cell wall polymers and phage lysis of Lactobacillus plantarum.

Authors:  L J Douglas; M J Wolin
Journal:  Biochemistry       Date:  1971-04-27       Impact factor: 3.162

6.  Improved medium for lactic streptococci and their bacteriophages.

Authors:  B E Terzaghi; W E Sandine
Journal:  Appl Microbiol       Date:  1975-06

7.  Accelerated adsorption of bacteriophage T5 to Escherichia coli F, resulting from reversible tail fiber-lipopolysaccharide binding.

Authors:  K Heller; V Braun
Journal:  J Bacteriol       Date:  1979-07       Impact factor: 3.490

8.  Mechanism of adsorption and eclipse of bacteriophage phi X174. II. Attachment and eclipse with isolated Escherichia coli cell wall lipopolysaccharide.

Authors:  N L Incardona; L Selvidge
Journal:  J Virol       Date:  1973-05       Impact factor: 5.103

9.  Bacteriophage lambda receptor site on the Escherichia coli K-12 LamB protein.

Authors:  K Gehring; A Charbit; E Brissaud; M Hofnung
Journal:  J Bacteriol       Date:  1987-05       Impact factor: 3.490

10.  Studies on streptococcal bacteriophages. II. Adsorption studies on group A and group C streptococcal bacteriophages.

Authors:  V A Fischetti; J B Zabriskie
Journal:  J Exp Med       Date:  1968-03-01       Impact factor: 14.307

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  22 in total

1.  Identification of the lower baseplate protein as the antireceptor of the temperate lactococcal bacteriophages TP901-1 and Tuc2009.

Authors:  Christina S Vegge; Finn K Vogensen; Stephen Mc Grath; Horst Neve; Douwe van Sinderen; Lone Brøndsted
Journal:  J Bacteriol       Date:  2006-01       Impact factor: 3.490

2.  Lactococcal bacteriophages require a host cell wall carbohydrate and a plasma membrane protein for adsorption and ejection of DNA.

Authors:  M R Monteville; B Ardestani; B L Geller
Journal:  Appl Environ Microbiol       Date:  1994-09       Impact factor: 4.792

3.  The entry mechanism of membrane-containing phage Bam35 infecting Bacillus thuringiensis.

Authors:  Ausra Gaidelyte; Virginija Cvirkaite-Krupovic; Rimantas Daugelavicius; Jaana K H Bamford; Dennis H Bamford
Journal:  J Bacteriol       Date:  2006-08       Impact factor: 3.490

4.  Crystal structure of a chimeric receptor binding protein constructed from two lactococcal phages.

Authors:  Marina Siponen; Silvia Spinelli; Stéphanie Blangy; Sylvain Moineau; Christian Cambillau; Valérie Campanacci
Journal:  J Bacteriol       Date:  2009-03-13       Impact factor: 3.490

Review 5.  Bacteriophage resistance in Lactococcus.

Authors:  P K Dinsmore; T R Klaenhammer
Journal:  Mol Biotechnol       Date:  1995-12       Impact factor: 2.695

6.  Lack of surface receptors not restriction-modification system determines F4 phage resistance in Streptococcus bovis II/1.

Authors:  I Styriak; P Pristas; P Javorský
Journal:  Folia Microbiol (Praha)       Date:  1998       Impact factor: 2.099

Review 7.  Structures and host-adhesion mechanisms of lactococcal siphophages.

Authors:  Silvia Spinelli; David Veesler; Cecilia Bebeacua; Christian Cambillau
Journal:  Front Microbiol       Date:  2014-01-16       Impact factor: 5.640

8.  Characterization of lipoteichoic acids as Lactobacillus delbrueckii phage receptor components.

Authors:  Liisa Räisänen; Karin Schubert; Tiina Jaakonsaari; Tapani Alatossava
Journal:  J Bacteriol       Date:  2004-08       Impact factor: 3.490

9.  Cloning of a chromosomal gene required for phage infection of Lactococcus lactis subsp. lactis C2.

Authors:  B L Geller; R G Ivey; J E Trempy; B Hettinger-Smith
Journal:  J Bacteriol       Date:  1993-09       Impact factor: 3.490

10.  Wall teichoic acids restrict access of bacteriophage endolysin Ply118, Ply511, and PlyP40 cell wall binding domains to the Listeria monocytogenes peptidoglycan.

Authors:  Marcel R Eugster; Martin J Loessner
Journal:  J Bacteriol       Date:  2012-09-21       Impact factor: 3.490

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