Literature DB >> 7028137

A new test based on 'salting out' to measure relative surface hydrophobicity of bacterial cells.

M Lindahl, A Faris, T Wadström, S Hjertén.   

Abstract

A simple method for quantification of the hydrophobic surface properties of bacteria is described. The method is based on precipitation of cells by salts, for instance (NH4)2SO4. The order in which cells are precipitated is a measure of their surface hydrophobicities, the most hydrophobic cells being first precipitated at low salt concentration. Temperature, pH, time and the bacterial cell concentration were shown to affect the results. When these variables were kept constant the method was highly reproducible. This 'salting out' method was applied to enterotoxigenic Escherichia coli strains with different surface protein antigens (fimbriae, fibrillae and colonization factor antigen, CFA). These enterotoxigenic E. coli strains were found to have surface hydrophobicity in the following order: CFA/I greater than CFA/II greater than K88 similar to K99 greater than type 1.

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Year:  1981        PMID: 7028137     DOI: 10.1016/0304-4165(81)90261-0

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  75 in total

1.  Characteristics of Escherichia coli isolates from infantile and childhood diarrhea.

Authors:  M Jayasheela; N Kumari; R K Shandil; S N Saxena
Journal:  Indian J Pediatr       Date:  1989 Jan-Feb       Impact factor: 1.967

2.  Hydrophobicity, adhesion, and surface-exposed proteins of gliding bacteria.

Authors:  M L Sorongon; R A Bloodgood; R P Burchard
Journal:  Appl Environ Microbiol       Date:  1991-11       Impact factor: 4.792

3.  Contact angle measurement and cell hydrophobicity of granular sludge from upflow anaerobic sludge bed reactors.

Authors:  D Daffonchio; J Thaveesri; W Verstraete
Journal:  Appl Environ Microbiol       Date:  1995-10       Impact factor: 4.792

4.  Contribution of silver ion resistance to the pathogenicity of Pseudomonas aeruginosa with special reference to burn wound sepsis.

Authors:  R Vasishta; M Saxena; S Chhibber
Journal:  Folia Microbiol (Praha)       Date:  1991       Impact factor: 2.099

5.  Expression of surface hydrophobicity encoded by R-plasmids in Escherichia coli laboratory strains.

Authors:  C M Ferreirós; M T Criado
Journal:  Arch Microbiol       Date:  1984-07       Impact factor: 2.552

6.  Functional heterogeneity of intestinal Escherichia coli strains expressing type 1 somatic pili (fimbriae): assessment of bacterial adherence to intestinal membranes and surface hydrophobicity.

Authors:  P M Sherman; W L Houston; E C Boedeker
Journal:  Infect Immun       Date:  1985-09       Impact factor: 3.441

7.  Interaction of Escherichia coli with different fimbriae and polymorphonuclear leukocytes.

Authors:  B Björkstén; T Wadström
Journal:  Infect Immun       Date:  1982-10       Impact factor: 3.441

8.  Relative hydrophobicities of Actinomyces viscosus and Actinomyces naeslundii strains and their adsorption to saliva-treated hydroxyapatite.

Authors:  W B Clark; M D Lane; J E Beem; S L Bragg; T T Wheeler
Journal:  Infect Immun       Date:  1985-03       Impact factor: 3.441

9.  Pathogenicity of Vibrio alginolyticus for cultured gilt-head sea bream (Sparus aurata L.).

Authors:  M C Balebona; M J Andreu; M A Bordas; I Zorrilla; M A Moriñigo; J J Borrego
Journal:  Appl Environ Microbiol       Date:  1998-11       Impact factor: 4.792

10.  Virulence of capsulated and noncapsulated isolates of Pasteurella multocida and their adherence to porcine respiratory tract cells and mucus.

Authors:  M Jacques; M Kobisch; M Bélanger; F Dugal
Journal:  Infect Immun       Date:  1993-11       Impact factor: 3.441

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