Literature DB >> 711665

Heterogeneity and distribution of lipopolysaccharide in the cell wall of a gram-negative marine bacterium.

J M DiRienzo, C F Deneke, R A MacLeod.   

Abstract

Lipopolysaccharide (LPS) extracted from Alteromonas haloplanktis 214, variants 1 and 3, separated into three fractions when subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The fractions appeared in the gels as bands which stained for carbohydrate with the periodate-Schiff reagent. Variant 1, a smooth variant of the organism, and variant 3, a rough colonial variant, produced identical banding patterns. Under similar conditions, LPS from Neisseria meningitidis SDIC, Escherichia coli O111:B4, and Salmonella typhimurium LT2 gave rise to one, two, and three bands, respectively. LPS from Pseudomonas aeruginosa (ATCC 9027) failed to stain clearly with the reagent used. The banding pattern obtained with A. haloplanktis LPS was found not to be due to artifacts produced by the extraction or solubilization procedures employed or to the amount of protein associated with the LPS. When Triton X-100 replaced sodium dodecyl sulfate in the electrophoresis system, LPS failed to migrate into the gel. The lipid A but not the degraded polysaccharide fraction obtained by mild acid hydrolysis of the LPS migrated into the gel on electrophoresis. The three carbohydrate-staining bands obtained with A. haloplanktis LPS and referred to as LPS I, II, and III, in order of increasing electrophoretic mobility, were detected in each of the three outer layers of the cell wall of the organism. Estimations from densitometer scans indicated that 17% of the total LPS in the cell was present in the outer membrane, with the remainder divided almost equally between the loosely bound outer layer and the periplasmic space. Of the three fractions, LPS II was present in each of the layers in greatest amounts. Less LPS I and more LPS III were present in the outer membrane than in the periplasmic space. Pulse-labeling studies indicated that LPS I and II may be synthesized independently, whereas LPS III, which appeared only in cells in the stationary phase of growth, may be a degradation product of LPS I.

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Year:  1978        PMID: 711665      PMCID: PMC218644          DOI: 10.1128/jb.136.1.148-157.1978

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


  20 in total

1.  Mechanism of assembly of the outer membrane of Salmonella typhimurium. Isolation and characterization of cytoplasmic and outer membrane.

Authors:  M J Osborn; J E Gander; E Parisi; J Carson
Journal:  J Biol Chem       Date:  1972-06-25       Impact factor: 5.157

2.  Glycoprotein staining following electrophoresis on acrylamide gels.

Authors:  R M Zacharius; T E Zell; J H Morrison; J J Woodlock
Journal:  Anal Biochem       Date:  1969-07       Impact factor: 3.365

3.  Dissociation in a marine pseudomonad.

Authors:  J A Gow; U W DeVoe; R A MacLeod
Journal:  Can J Microbiol       Date:  1973-06       Impact factor: 2.419

4.  Cell walls, lipids, and lipopolysaccharides of Pseudomonas species.

Authors:  S G Wilkinson; L Galbraith; G A Lightfoot
Journal:  Eur J Biochem       Date:  1973-02-15

5.  Molecular weight estimation of polypeptide chains by electrophoresis in SDS-polyacrylamide gels.

Authors:  A L Shapiro; E Viñuela; J V Maizel
Journal:  Biochem Biophys Res Commun       Date:  1967-09-07       Impact factor: 3.575

6.  Heterogeneity of lipopolysaccharides. Analysis of polysaccharide chain lengths by sodium dodecylsulfate-polyacrylamide gel electrophoresis.

Authors:  B Jann; K Reske; K Jann
Journal:  Eur J Biochem       Date:  1975-12-01

7.  Distribution of lipopolysaccharide and the detection of a new subfraction in the cell envelope of a marine pseudomonad.

Authors:  J D Nelson; R A Macleod
Journal:  J Bacteriol       Date:  1977-02       Impact factor: 3.490

8.  Composition of the fractions separated by polyacrylamide gel electrophoresis of the lipopolysaccharide of a marine bacterium.

Authors:  J M DiRienzo; R A MacLeod
Journal:  J Bacteriol       Date:  1978-10       Impact factor: 3.490

9.  SDS-polyacrylamide gel electrophoresis of lipopolysaccharides.

Authors:  R R Russell; K G Johnson
Journal:  Can J Microbiol       Date:  1975-12       Impact factor: 2.419

10.  Release of endotoxin in the form of cell wall blebs during in vitro growth of Neisseria meningitidis.

Authors:  I W Devoe; J E Gilchrist
Journal:  J Exp Med       Date:  1973-11-01       Impact factor: 14.307

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  5 in total

1.  O-antigen conversion in Pseudomonas aeruginosa PAO1 by bacteriophage D3.

Authors:  J Kuzio; A M Kropinski
Journal:  J Bacteriol       Date:  1983-07       Impact factor: 3.490

2.  Composition of the fractions separated by polyacrylamide gel electrophoresis of the lipopolysaccharide of a marine bacterium.

Authors:  J M DiRienzo; R A MacLeod
Journal:  J Bacteriol       Date:  1978-10       Impact factor: 3.490

3.  Pyocin-resistant lipopolysaccharide mutans of Neisseria gonorrhoeae: alterations in sensitivity to normal human serum and polymyxin B.

Authors:  L F Guymon; M Esser; W M Shafer
Journal:  Infect Immun       Date:  1982-05       Impact factor: 3.441

4.  Isolation of two protein-free and chemically different lipopolysaccharides from Bordetella pertussis phenol-extracted endotoxin.

Authors:  A Le Dur; R Chaby; L Szabó
Journal:  J Bacteriol       Date:  1980-07       Impact factor: 3.490

5.  Chemical and chromatographic analysis of lipopolysaccharide from an antibiotic-supersusceptible mutant of Pseudomonas aeruginosa.

Authors:  A M Kropinski; J Kuzio; B L Angus; R E Hancock
Journal:  Antimicrob Agents Chemother       Date:  1982-02       Impact factor: 5.191

  5 in total

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