Literature DB >> 6409883

Spontaneous release of lipopolysaccharide by Pseudomonas aeruginosa.

J E Cadieux, J Kuzio, F H Milazzo, A M Kropinski.   

Abstract

Pseudomonas aeruginosa PAO grown in glucose mineral salts medium released lipopolysaccharide which was chemically and immunologically similar to the cellular lipopolysaccharide. In addition, it possessed identical phage E79-inactivating properties. Through neutralization of phage activity and hemolysis inhibition assays, the organism was found to liberate lipopolysaccharide at a constant rate during log-phase growth equivalent to 1.3 to 2.2 ng/10(8) cells over a growth temperature range of 25 to 42 degrees C. At 19 degrees C, a lipopolysaccharide was released which was deficient in phage-inactivating activity but retained its immunological properties. Chemical analysis of lipopolysaccharide extracted from cells grown at 19 degrees C showed a deficiency in the O-side-chain component fucosamine. Gel exclusion chromatography of the polysaccharide fraction derived from lipopolysaccharide isolated from cells grown at 19 degrees C exhibited a decreased content of side-chain polysaccharide as well as a difference in the hexosamine:hexose ratio. The results of sodium dodecyl sulfate-polyacrylamide gel electrophoretic analysis confirmed these results as well as establishing that an essentially normal distribution of side-chain repeating unit lengths were to be found in the 19 degrees C preparation. These results suggest a decrease in the frequency of capping R-form lipopolysaccharide at 19 degrees C.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6409883      PMCID: PMC217754          DOI: 10.1128/jb.155.2.817-825.1983

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


  35 in total

1.  Indirect bacterial hemagglutination, and its application to the study of bacterial antigens and serologic diagnosis.

Authors:  E Neter
Journal:  Pathol Microbiol (Basel)       Date:  1965

2.  Prevention of death from endotoxin with antisera. I. The risk of fatal anaphylaxis to endotoxin.

Authors:  C E Davis; K R Brown; H Douglas; W J Tate; A I Braude
Journal:  J Immunol       Date:  1969-03       Impact factor: 5.422

3.  Free Endotoxin.

Authors:  M J Crutchley; D G Marsh; J Cameron
Journal:  Nature       Date:  1967-06-03       Impact factor: 49.962

4.  Biological studies on free endotoxin and a non-toxic material from culture supernatant fluids of Escherichia coli 078K80.

Authors:  M J Crutchley; D G Marsh; J Cameron
Journal:  J Gen Microbiol       Date:  1968-03

5.  Improved method of hexosamine determination.

Authors:  A R Johnson
Journal:  Anal Biochem       Date:  1971-12       Impact factor: 3.365

6.  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

7.  Release of somatic antigen into filtrates of an Escherichia coli broth culture. A preliminary report.

Authors:  J C Guckian; J E Perry
Journal:  Tex Rep Biol Med       Date:  1966

8.  Preparation and properties of antisera against the lipid-A component of bacterial lipopolysaccharides.

Authors:  C Galanos; O Lüderitz; O Westphal
Journal:  Eur J Biochem       Date:  1971-12-22

9.  Relation between excreted lipopolysaccharide complexes and surface structures of a lysine-limited culture of Escherichia coli.

Authors:  K W Knox; M Vesk; E Work
Journal:  J Bacteriol       Date:  1966-10       Impact factor: 3.490

10.  Chemical and biological properties of an extracellular lipopolysaccharide from Escherichia coli grown under lysine-limiting conditions.

Authors:  A Taylor; K W Knox; E Work
Journal:  Biochem J       Date:  1966-04       Impact factor: 3.857

View more
  18 in total

1.  Use of fluorescent lectin probes for analysis of footprints from Pseudomonas aeruginosa MDC on hydrophilic and hydrophobic glass substrata.

Authors:  Eduardo Mora Bejarano; René Peter Schneider
Journal:  Appl Environ Microbiol       Date:  2004-07       Impact factor: 4.792

2.  Rhizobium leguminosarum CFN42 genetic regions encoding lipopolysaccharide structures essential for complete nodule development on bean plants.

Authors:  J R Cava; P M Elias; D A Turowski; K D Noel
Journal:  J Bacteriol       Date:  1989-01       Impact factor: 3.490

3.  Prevalence of surface swarming behavior in Salmonella.

Authors:  Wook Kim; Michael G Surette
Journal:  J Bacteriol       Date:  2005-09       Impact factor: 3.490

4.  Purification of extracellular lipase from Pseudomonas aeruginosa.

Authors:  W Stuer; K E Jaeger; U K Winkler
Journal:  J Bacteriol       Date:  1986-12       Impact factor: 3.490

5.  Immunochemical and biochemical analysis of the polyvalent Pseudomonas aeruginosa vaccine PEV.

Authors:  S MacIntyre; T McVeigh; P Owen
Journal:  Infect Immun       Date:  1986-02       Impact factor: 3.441

Review 6.  Pseudomonas biofilm matrix composition and niche biology.

Authors:  Ethan E Mann; Daniel J Wozniak
Journal:  FEMS Microbiol Rev       Date:  2012-01-23       Impact factor: 16.408

Review 7.  Clinical relevance of antibiotic-induced endotoxin release.

Authors:  J M Prins; S J van Deventer; E J Kuijper; P Speelman
Journal:  Antimicrob Agents Chemother       Date:  1994-06       Impact factor: 5.191

8.  Genetics of swarming motility in Salmonella enterica serovar typhimurium: critical role for lipopolysaccharide.

Authors:  A Toguchi; M Siano; M Burkart; R M Harshey
Journal:  J Bacteriol       Date:  2000-11       Impact factor: 3.490

9.  Quantitation and biological properties of released and cell-bound lipooligosaccharides from nontypeable Haemophilus influenzae.

Authors:  X X Gu; C M Tsai; M A Apicella; D J Lim
Journal:  Infect Immun       Date:  1995-10       Impact factor: 3.441

10.  Comparative immunochemistry of lipopolysaccharides from typable and polyagglutinable Pseudomonas aeruginosa strains isolated from patients with cystic fibrosis.

Authors:  A Fomsgaard; R S Conrad; C Galanos; G H Shand; N Høiby
Journal:  J Clin Microbiol       Date:  1988-05       Impact factor: 5.948

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.