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Purification and partial characterization of the opacity-associated proteins of Neisseria gonorrhoeae

Gonococci, grown on agar, frequently give rise to opaque colonies. This opacity phenotype is associated with the presence of one or more outer membrane proteins of approximately 28,000 mol weight. These proteins are included within a class of proteins named proteins II. A method is described to isol...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1984
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187218/
https://www.ncbi.nlm.nih.gov/pubmed/6420502
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description Gonococci, grown on agar, frequently give rise to opaque colonies. This opacity phenotype is associated with the presence of one or more outer membrane proteins of approximately 28,000 mol weight. These proteins are included within a class of proteins named proteins II. A method is described to isolate and purify the opacity-associated proteins from Neisseria gonorrhoeae. This method uses high concentrations of calcium and a zwitterionic detergent at pH 4.0. Under these conditions proteins II are readily solubilized from the outer membrane. Further purification is achieved by ion exchange and molecular sieve chromatography in the presence of the zwitterionic detergent. The opacity-associated proteins are very basic with isoelectric points varying between 9.0 to 10.0. Further evidence for their basic nature is their behavior on ion exchange chromatography and their amino acid composition.
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spelling pubmed-21872182008-04-17 Purification and partial characterization of the opacity-associated proteins of Neisseria gonorrhoeae J Exp Med Articles Gonococci, grown on agar, frequently give rise to opaque colonies. This opacity phenotype is associated with the presence of one or more outer membrane proteins of approximately 28,000 mol weight. These proteins are included within a class of proteins named proteins II. A method is described to isolate and purify the opacity-associated proteins from Neisseria gonorrhoeae. This method uses high concentrations of calcium and a zwitterionic detergent at pH 4.0. Under these conditions proteins II are readily solubilized from the outer membrane. Further purification is achieved by ion exchange and molecular sieve chromatography in the presence of the zwitterionic detergent. The opacity-associated proteins are very basic with isoelectric points varying between 9.0 to 10.0. Further evidence for their basic nature is their behavior on ion exchange chromatography and their amino acid composition. The Rockefeller University Press 1984-02-01 /pmc/articles/PMC2187218/ /pubmed/6420502 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Purification and partial characterization of the opacity-associated proteins of Neisseria gonorrhoeae
title Purification and partial characterization of the opacity-associated proteins of Neisseria gonorrhoeae
title_full Purification and partial characterization of the opacity-associated proteins of Neisseria gonorrhoeae
title_fullStr Purification and partial characterization of the opacity-associated proteins of Neisseria gonorrhoeae
title_full_unstemmed Purification and partial characterization of the opacity-associated proteins of Neisseria gonorrhoeae
title_short Purification and partial characterization of the opacity-associated proteins of Neisseria gonorrhoeae
title_sort purification and partial characterization of the opacity-associated proteins of neisseria gonorrhoeae
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187218/
https://www.ncbi.nlm.nih.gov/pubmed/6420502