Literature DB >> 3312487

Novobiocin-resistant mutants of Streptococcus sanguis with reduced cell hydrophobicity and defective in coaggregation.

H F Jenkinson1.   

Abstract

Mutants of Streptococcus sanguis resistant to novobiocin (NovR-mutants) were isolated after mutagenesis of strain Challis with ethyl methanesulphonate. The resistance phenotype was transferred by DNA-mediated transformation back into the parent strain at high frequency suggesting resistance was due to mutation(s) in a single gene or in closely-linked genes. Cells of NovR-mutants had normal morphology and secreted similar proteins to the wild-type strain. However, mutant cultures had slower growth rates, the mutant cells had reduced hydrophobicity, and they showed a reduced degree of coaggregation with Actinomyces viscosus and Actinomyces naeslundii. Cell envelopes prepared from NovR-mutants differed from wild-type cell envelopes in that they (a) were impaired in ability to coaggregate with A. viscosus cells, and (b) had altered protein composition as detected by SDS-PAGE. The results suggest that hydrophobic proteins in the cell envelope of S. sanguis may be necessary for coaggregation of this bacterium with actinomycetes.

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Year:  1987        PMID: 3312487     DOI: 10.1099/00221287-133-7-1909

Source DB:  PubMed          Journal:  J Gen Microbiol        ISSN: 0022-1287


  16 in total

1.  Broad-host-range shuttle vectors for screening of regulated promoter activity in viridans group streptococci: isolation of a pH-regulated promoter.

Authors:  A J Vriesema; R Brinkman; J Kok; J Dankert; S A Zaat
Journal:  Appl Environ Microbiol       Date:  2000-02       Impact factor: 4.792

2.  LuxS-based signaling in Streptococcus gordonii: autoinducer 2 controls carbohydrate metabolism and biofilm formation with Porphyromonas gingivalis.

Authors:  Roderick McNab; Suzannah K Ford; Azza El-Sabaeny; Bruno Barbieri; Guy S Cook; Richard J Lamont
Journal:  J Bacteriol       Date:  2003-01       Impact factor: 3.490

3.  The Streptococcus gordonii Adhesin CshA Protein Binds Host Fibronectin via a Catch-Clamp Mechanism.

Authors:  Catherine R Back; Maryta N Sztukowska; Marisa Till; Richard J Lamont; Howard F Jenkinson; Angela H Nobbs; Paul R Race
Journal:  J Biol Chem       Date:  2016-12-05       Impact factor: 5.157

4.  Cell surface polypeptide CshA mediates binding of Streptococcus gordonii to other oral bacteria and to immobilized fibronectin.

Authors:  R McNab; A R Holmes; J M Clarke; G W Tannock; H F Jenkinson
Journal:  Infect Immun       Date:  1996-10       Impact factor: 3.441

5.  Insertional inactivation of the gene encoding a 76-kilodalton cell surface polypeptide in Streptococcus gordonii Challis has a pleiotropic effect on cell surface composition and properties.

Authors:  H F Jenkinson; R A Easingwood
Journal:  Infect Immun       Date:  1990-11       Impact factor: 3.441

6.  Role of Streptococcus gordonii amylase-binding protein A in adhesion to hydroxyapatite, starch metabolism, and biofilm formation.

Authors:  J D Rogers; R J Palmer; P E Kolenbrander; F A Scannapieco
Journal:  Infect Immun       Date:  2001-11       Impact factor: 3.441

7.  Multiple adhesin proteins on the cell surface of Streptococcus gordonii are involved in adhesion to human fibronectin.

Authors:  Nicholas S Jakubovics; Jane L Brittan; Lindsay C Dutton; Howard F Jenkinson
Journal:  Microbiology (Reading)       Date:  2009-08-06       Impact factor: 2.777

8.  Adherence, coaggregation, and hydrophobicity of Streptococcus gordonii associated with expression of cell surface lipoproteins.

Authors:  H F Jenkinson
Journal:  Infect Immun       Date:  1992-03       Impact factor: 3.441

9.  Inactivation of the gene encoding surface protein SspA in Streptococcus gordonii DL1 affects cell interactions with human salivary agglutinin and oral actinomyces.

Authors:  H F Jenkinson; S D Terry; R McNab; G W Tannock
Journal:  Infect Immun       Date:  1993-08       Impact factor: 3.441

10.  A binding-lipoprotein-dependent oligopeptide transport system in Streptococcus gordonii essential for uptake of hexa- and heptapeptides.

Authors:  H F Jenkinson; R A Baker; G W Tannock
Journal:  J Bacteriol       Date:  1996-01       Impact factor: 3.490

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