Literature DB >> 1375

Effect of alkali on the structure of cell envelopes of Chlamydia psittaci elementary bodies.

T Narita, P B Wyrick, G P Manire.   

Abstract

Suspensions of isolated cell envelopes of infectious elementary bodies (EB) of Chlamydia psittaci at alkaline pH showed a rapid, extensive decrease in absorbance, accompanied by the release of a cell envelope component in a sedimentable form. This phenomenon was observed both at 0 C and with envelopes which had been previously heated to 100 C. Monovalent and divalent cations effectively inhibited the turbidity loss, whereas ethylenediaminetetraacetate (EDTA) caused an accelerated decrease in turbidity. The turbidity loss observed after incubation of the envelopes at alkaline pH could be reversed to the level of the initial value by dialysis against distilled water containing Mg2+. Thin-section electron photomicrographs of purified EB exposed to alkaline buffer with EDTA revealed the loss of the internal contents of cells, but these cells still maintained their round shapes. The cell surface of treated EB appeared pitted in negatively stained preparations, whereas intact EB had a smooth surface. Electron microscopic studies on negatively stained preparations of the clear supernatant obtained after the treatment of the envelope with alkaline buffer containing EDTA demonstrated the presence of spherical particles, approximately 6 to 7 nm in diameter, and rodlike particles, which appeared to be made up of two or more spherical particles.

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Year:  1976        PMID: 1375      PMCID: PMC233363          DOI: 10.1128/jb.125.1.300-307.1976

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


  27 in total

Review 1.  ASPECTS OF BACTERIAL RESPONSE TO THE IONIC ENVIRONMENT.

Authors:  A D BROWN
Journal:  Bacteriol Rev       Date:  1964-09

2.  Role of Multivalent Cations in the Organization, Structure, and Assembly of the Cell Wall of Pseudomonas aeruginosa.

Authors:  M A Asbell; R G Eagon
Journal:  J Bacteriol       Date:  1966-08       Impact factor: 3.490

3.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

4.  Electron microscopic studies on mode of action of polymyxin.

Authors:  M Koike; K Iida; T Matsuo
Journal:  J Bacteriol       Date:  1969-01       Impact factor: 3.490

5.  Release of lipopolysaccharide by EDTA treatment of E. coli.

Authors:  L Leive
Journal:  Biochem Biophys Res Commun       Date:  1965-11-22       Impact factor: 3.575

6.  Characterization of the membranes of Thermoplasma acidophilum.

Authors:  P F Smith; T A Langworth; W R Mayberry; A E Houghland
Journal:  J Bacteriol       Date:  1973-11       Impact factor: 3.490

7.  Electron microscope observations on the effects of polymixin B sulfate on cell walls of Chlamydia psittaci.

Authors:  A Matsumoto; N Higashi; A Tamura
Journal:  J Bacteriol       Date:  1973-01       Impact factor: 3.490

8.  Freeze-etch study of Pseudomonas aeruginosa: localization within the cell wall of an ethylenediaminetetraacetate-extractable.

Authors:  H E Gilleland; J D Stinnett; I L Roth; R G Eagon
Journal:  J Bacteriol       Date:  1973-01       Impact factor: 3.490

9.  Dissociation and reassembly of Escherichia coli outer membrane and of lipopolysaccharide, and their reassembly onto flagellar basal bodies.

Authors:  M L DePamphilis
Journal:  J Bacteriol       Date:  1971-03       Impact factor: 3.490

10.  Electron Microscopic Observations on the Fine Structure of Cell Walls of Chlamydia psittaci.

Authors:  A Matsumoto; G P Manire
Journal:  J Bacteriol       Date:  1970-12       Impact factor: 3.490

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  10 in total

1.  Chlamydia trachomatis developmentally regulated protein is homologous to eukaryotic histone H1.

Authors:  T Hackstadt; W Baehr; Y Ying
Journal:  Proc Natl Acad Sci U S A       Date:  1991-05-01       Impact factor: 11.205

2.  Protein-carbohydrate-lipid complex isolated from the cell envelopes of Chlamydia psittaci in alkaline buffer and ethylenediaminetetraacetate.

Authors:  T Narita; G P Manire
Journal:  J Bacteriol       Date:  1976-01       Impact factor: 3.490

3.  Factors influencing the infectivity of Chlamydia pneumoniae elementary bodies on HL cells.

Authors:  J J Theunissen; B Y van Heijst; J H Wagenvoort; E Stolz; M F Michel
Journal:  J Clin Microbiol       Date:  1992-06       Impact factor: 5.948

4.  Purification and N-terminal amino acid sequences of Chlamydia trachomatis histone analogs.

Authors:  T Hackstadt
Journal:  J Bacteriol       Date:  1991-11       Impact factor: 3.490

5.  Nonoxidative antimicrobial effects of human polymorphonuclear leukocyte granule proteins on Chlamydia spp. in vitro.

Authors:  K B Register; C H Davis; P B Wyrick; W M Shafer; J K Spitznagel
Journal:  Infect Immun       Date:  1987-10       Impact factor: 3.441

6.  Parasite-specified phagocytosis of Chlamydia psittaci and Chlamydia trachomatis by L and HeLa cells.

Authors:  G I Byrne; J W Moulder
Journal:  Infect Immun       Date:  1978-02       Impact factor: 3.441

7.  Effects of nonionic, ionic, and dipolar ionic detergents and EDTA on the Brucella cell envelope.

Authors:  I Moriyon; D T Berman
Journal:  J Bacteriol       Date:  1982-11       Impact factor: 3.490

8.  Vesicles containing Chlamydia trachomatis serovar L2 remain above pH 6 within HEC-1B cells.

Authors:  N Schramm; C R Bagnell; P B Wyrick
Journal:  Infect Immun       Date:  1996-04       Impact factor: 3.441

9.  Architecture of the cell envelope of Chlamydia psittaci 6BC.

Authors:  K D Everett; T P Hatch
Journal:  J Bacteriol       Date:  1995-02       Impact factor: 3.490

10.  Purification and partial characterization of the major outer membrane protein of Chlamydia trachomatis.

Authors:  H D Caldwell; J Kromhout; J Schachter
Journal:  Infect Immun       Date:  1981-03       Impact factor: 3.441

  10 in total

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