Literature DB >> 1376

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

T Narita, G P Manire.   

Abstract

Exposure of isolated cell envelopes from purified infectious elementary (EB) of Chlamydia psittaci to sodium carbonate-bicarbonate buffer at pH 10 plus ethylenediaminetetraacetate (EDTA) results in partial solubilization of the total protein. The released materials represent 20% of the dry weight, 16% of the total protein, 40% of the total carbohydrate, and 9% of the total lipid of the cell envelopes. Sucrose density gradient centrifugation, and Sephadex G-200, Sepharose 4B, or diethylaminoethyl-cellulose column chromatography, reveal a protein-carbohydrate-lipid complex of several hundred thousand molecular weight that contains 50% protein. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of the isolated EB cell envelopes reveals two major protein bands, A and B, with estimated molecular masses of approximately 85,000 and 53,000, respectively, both of which also stain for the presence of carbohydrate and lipid. Gel electrophoresis of the protein-carbohydrate-lipid complex reveals two protein bands, C and D, with estimated molecular weights of approximately 17,000 and 13,000, respectively, which contain lipid and a small amount of carbohydrate; bands A and B are not present in the complex. Gel electrophoresis of the cell envelope residues after extraction of the complex with alkali and EDTA shows a single main band, corresponding to the position of band B, which contains protein, carbohydrate, and lipid; band A is completely missing. B and A is believed to be a component of the complex, which is split into two subunits on alkali solubilization.

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Year:  1976        PMID: 1376      PMCID: PMC233364          DOI: 10.1128/jb.125.1.308-316.1976

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


  23 in total

1.  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

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

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

3.  Proteins and glycoproteins of the erythrocyte membrane.

Authors:  D Kobylka; A Khettry; B C Shin; K L Carraway
Journal:  Arch Biochem Biophys       Date:  1972-02       Impact factor: 4.013

4.  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

5.  Examination of the protein composition of the cell envelope of Escherichia coli by polyacrylamide gel electrophoresis.

Authors:  C A Schnaitman
Journal:  J Bacteriol       Date:  1970-11       Impact factor: 3.490

6.  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

7.  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

8.  Separation of the polypeptides of Chlamydia and its cell walls by polyacrylamide gel electrophoresis.

Authors:  A Tamura; A Tanaka; G P Manire
Journal:  J Bacteriol       Date:  1974-04       Impact factor: 3.490

9.  Proteins released from cell envelopes of Pseudomonas aeruginosa on exposure to ethylenediaminetetraacetate: comparison with dimethylformamide-extractable proteins.

Authors:  J D Stinnett; H E Gilleland; R G Eagon
Journal:  J Bacteriol       Date:  1973-04       Impact factor: 3.490

10.  Homogeneity of envelope proteins of Escherichia coli separated by gel electrophoresis in sodium dodecyl sulfate.

Authors:  M Inouye; M L Yee
Journal:  J Bacteriol       Date:  1973-01       Impact factor: 3.490

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  6 in total

Review 1.  The chlamydia: molecular biology of procaryotic obligate parasites of eucaryocytes.

Authors:  Y Becker
Journal:  Microbiol Rev       Date:  1978-06

2.  Response of C3H/HeJ and C3H/HeN mice and their peritoneal macrophages to the toxicity of Chlamydia psittaci elementary bodies.

Authors:  B E Ivins; P B Wyrick
Journal:  Infect Immun       Date:  1978-11       Impact factor: 3.441

3.  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

4.  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

5.  Identification of a major envelope protein in Chlamydia spp.

Authors:  T P Hatch; D W Vance; E Al-Hossainy
Journal:  J Bacteriol       Date:  1981-04       Impact factor: 3.490

6.  Molecular cloning and expression of Chlamydia trachomatis major outer membrane protein antigens in Escherichia coli.

Authors:  R S Stephens; C C Kuo; G Newport; N Agabian
Journal:  Infect Immun       Date:  1985-03       Impact factor: 3.441

  6 in total

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