Literature DB >> 3123455

Heterogeneity of lipopolysaccharides from Pseudomonas aeruginosa: analysis of lipopolysaccharide chain length.

M Rivera1, L E Bryan, R E Hancock, E J McGroarty.   

Abstract

Lipopolysaccharide (LPS) from smooth strains of Pseudomonas aeruginosa 503, PAZ1, PAO1715, PAO1716, and Z61 was fractionated by gel filtration chromatography. LPS samples from the first four strains, all PAO1 derivatives, separated into three major size populations, whereas LPS from strain Z61, a Pac K799/WT mutant strain, separated into two size populations. When column fractions were applied to sodium dodecyl sulfate-polyacrylamide gels in their order of elution, molecules of decreasing size were resolved, and the ladder of molecules with different-length O antigens formed a diagonal across the gel. The LPS from the PAO1 derivatives contained two distinct sets of bands, distinguished on the gels as two sets of diagonals. The set of bands with the faster mobility, the B bands, was found in column fractions comprising the three major amino sugar-containing peaks. In the sample from strain 503, a fourth minor peak which contained B bands was resolved. The slower-moving set of bands, the A bands, were recovered in a minor peak. LPS from strain Z61 contained only one set of bands, with the higher-molecular-weight molecules eluting from the column in a volume similar to that of the B bands of the PAO1 strains. Analysis of the fractions of LPS from all strains indicated that less than 8% of the LPS molecules had a long, attached O antigen. Analysis of the peak that contained mainly A bands indicated a lack of reactive amino sugar and phosphate, although heptose and 2-keto-3-deoxyoctulosonic acid were detected. Reaction of isolated fractions with monoclonal antibody specific for the PAO1 O-antigen side chain indicated that only the B bands from the PAO1 strains were antigenically reactive. The bands from strain Z61 showed no reactivity. The data suggest that the A and B bands from the PAO1 strains are antigenically distinct. We propose that PAO1 strains synthesize two types of molecules that are antigenically different.

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Year:  1988        PMID: 3123455      PMCID: PMC210683          DOI: 10.1128/jb.170.2.512-521.1988

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  51 in total

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2.  Procedure for determining heptose and hexose in lipopolysaccharides. Modification of the cysteine-sulfuric acid method.

Authors:  B G Wright; P A Rebers
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3.  Structural investigations on the 2-keto-3-deoxyoctonate region of lipopolysaccharides.

Authors:  W Dröge; V Lehmann; O Lüderitz; O Westphal
Journal:  Eur J Biochem       Date:  1970-05-01

Review 4.  Salmonella O antigens and virulence.

Authors:  R J Roantree
Journal:  Annu Rev Microbiol       Date:  1967       Impact factor: 15.500

5.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

6.  A new method for the extraction of R lipopolysaccharides.

Authors:  C Galanos; O Lüderitz; O Westphal
Journal:  Eur J Biochem       Date:  1969-06

7.  Do endotoxins devoid of 3-deoxy-D-manno-2-octulosonic acid exist?

Authors:  M Caroff; S Lebbar; L Szabó
Journal:  Biochem Biophys Res Commun       Date:  1987-03-30       Impact factor: 3.575

8.  The relationship between the O-antigenic lipopolysaccharides and serological specificity in strains of Pseudomonas aeruginosa of different O-serotypes.

Authors:  I R Chester; P M Meadow; T L Pitt
Journal:  J Gen Microbiol       Date:  1973-10

9.  A rapid procedure for the estimation of amino sugars on a micro scale.

Authors:  R Gatt; E R Berman
Journal:  Anal Biochem       Date:  1966-04       Impact factor: 3.365

10.  Mapping and characterization of two mutations to antibiotic supersusceptibility in Pseudomonas aeruginosa.

Authors:  B L Angus; J A Fyfe; R E Hancock
Journal:  J Gen Microbiol       Date:  1987-10
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  53 in total

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Review 2.  Membrane vesicle release in bacteria, eukaryotes, and archaea: a conserved yet underappreciated aspect of microbial life.

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Authors:  M Rivera; T R Chivers; J S Lam; E J McGroarty
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4.  Pseudomonas aeruginosa PAO1 ceases to express serotype-specific lipopolysaccharide at 45 degrees C.

Authors:  S A Makin; T J Beveridge
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5.  Resistance to pefloxacin in Pseudomonas aeruginosa.

Authors:  M Michea-Hamzehpour; C Lucain; J C Pechere
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6.  Defects in gliding motility in mutants of Cytophaga johnsonae lacking a high-molecular-weight cell surface polysaccharide.

Authors:  W Godchaux; M A Lynes; E R Leadbetter
Journal:  J Bacteriol       Date:  1991-12       Impact factor: 3.490

7.  Pseudomonas aeruginosa lipopolysaccharide: evidence that the O side chains and common antigens are on the same molecule.

Authors:  K Hatano; J B Goldberg; G B Pier
Journal:  J Bacteriol       Date:  1993-08       Impact factor: 3.490

8.  Interaction of gentamicin with the A band and B band lipopolysaccharides of Pseudomonas aeruginosa and its possible lethal effect.

Authors:  J L Kadurugamuwa; J S Lam; T J Beveridge
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9.  Immunochemical characterization of O polysaccharides composing the alpha-D-rhamnose backbone of lipopolysaccharide of Pseudomonas syringae and classification of bacteria into serogroups O1 and O2 with monoclonal antibodies.

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Journal:  J Bacteriol       Date:  1996-11       Impact factor: 3.490

10.  Mechanisms of Cation Exchange by Pseudomonas aeruginosa PAO1 and PAO1 wbpL, a Strain with a Truncated Lipopolysaccharide.

Authors:  J Shephard; A J McQuillan; P J Bremer
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