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Genetic and immunological studies on the expression in Escherichia coli of the class 1 outer membrane protein from Neisseria meningitidis

Genetic and immunological studies on the expression in Escherichia coli of the class 1 outer membrane protein from Neisseria meningitidis
Genetic and immunological studies on the expression in Escherichia coli of the class 1 outer membrane protein from Neisseria meningitidis

Meningoccal meningitis remains a severe life-threatening infection. Present vaccines to combat the disease consist of purified capsular polysac-charides and provide only limited protection against serogroups A & C, and give no protection against group B mcningococci. The class 1 outer membrane protein, may offer an alternative as an immunogen. Unfortunately, other components in the current experimental subcapsular vaccines, and the difficulty of obtaining class 1 protein in a native form, has hampered further investigation of its potential use in vaccines. This project uses recombinant techniques to express the class 1 protein in an E.coli host as the first step in production of an improved immunogen.

The entire class 1 gene porA had been cloned and sequenced and transferred to a plasmid vector pMTL20 (Barlow et a/., (1987

University of Southampton
White, Deborah Ann
8427772f-813c-4091-b245-b289b783dc08
White, Deborah Ann
8427772f-813c-4091-b245-b289b783dc08

White, Deborah Ann (1991) Genetic and immunological studies on the expression in Escherichia coli of the class 1 outer membrane protein from Neisseria meningitidis. University of Southampton, Doctoral Thesis.

Record type: Thesis (Doctoral)

Abstract

Meningoccal meningitis remains a severe life-threatening infection. Present vaccines to combat the disease consist of purified capsular polysac-charides and provide only limited protection against serogroups A & C, and give no protection against group B mcningococci. The class 1 outer membrane protein, may offer an alternative as an immunogen. Unfortunately, other components in the current experimental subcapsular vaccines, and the difficulty of obtaining class 1 protein in a native form, has hampered further investigation of its potential use in vaccines. This project uses recombinant techniques to express the class 1 protein in an E.coli host as the first step in production of an improved immunogen.

The entire class 1 gene porA had been cloned and sequenced and transferred to a plasmid vector pMTL20 (Barlow et a/., (1987

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Published date: 1991

Identifiers

Local EPrints ID: 460404
URI: http://eprints.soton.ac.uk/id/eprint/460404
PURE UUID: f76aab49-b16f-480d-9f4f-4214da524572

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Date deposited: 04 Jul 2022 18:21
Last modified: 22 Feb 2023 18:54

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Contributors

Author: Deborah Ann White

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