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Chemical and spectroscopic studies of the capsular polysaccharides of some Klebsiella serotypes

Includes bibliographical references.

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Main Author: Ravenscroft, Neil
Other Authors: Stephen, A M
Format: Thesis
Language:English
Published: Department of Chemistry 2016
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access_status_str Open Access
author Ravenscroft, Neil
author2 Stephen, A M
author_browse Ravenscroft, Neil
Stephen, A M
author_facet Stephen, A M
Ravenscroft, Neil
author_sort Ravenscroft, Neil
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/17186
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:34:38.153Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2016
publishDateRange 2016
publishDateSort 2016
publisher Department of Chemistry
publisherStr Department of Chemistry
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source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/17186 Chemical and spectroscopic studies of the capsular polysaccharides of some Klebsiella serotypes Ravenscroft, Neil Stephen, A M Polysaccharides Oligosaccharides Enterobacteriaceae Organic Chemistry Includes bibliographical references. As part of an international collaborative programme concerned with the elucidation of the molecular structures of capsular polysaccharides (the K-antigen) produced by strains of the bacterial genus Klebsiella, the capsular material of serotype K71 has been investigated, and that of serotypes K36 and K64 re-examined, by novel enzymic and spectroscopic methods. The cultivation and employment of bacteriophages which are capable of cleaving (by specific glycanase action) the isolated, cognate bacterial polysaccharide in vitro has yielded highly significant oligosaccharides. These may represent the repeating unit in the polysaccharide or be derivatives resulting from conversion of uronic acid to the 4,5-unsaturated analogue where, as found for serotype K64, the mode of cleavage is β-elimination not hydrolysis. The oligosaccharides thus generated have proved to be far more amenable to chemical and spectroscopic studies than their parent polymers, thereby facilitating complete characterisation of the molecular structures of the original polysaccharides. Chemical methods applied to these oligosaccharides included specific degradations by periodate oxidation and acid-, alkali- or enzyme- catalysed hydrolysis, products being identified by methylation analysis (involving the extensive use of gas-liquid chromatography coupled to mass spectrometry) and spectroscopic studies (mass and n.m.r.). During the course of these investigations it became apparent that the structures of the intact oligosaccharides (containing six or seven sugar residues) could be determined almost entirely from spectroscopic analysis, chiefly by detailed two-dimensional n.m.r. studies involving the use of high field spectrometers and the application of homo- and heteronuclear shift correlated spectroscopy, the sequence of sugar units being confirmed by mass spectrometric analysis of the permethylated derivatives. Methylation analysis of the oligosaccharides derived from Klebsiella serotype K36 proved that the glucuronic acid residue is linked through 0-2, and not 0-4 as published by others; this finding was corroborated during characterisation of the monomeric oligosaccharide by mass- and n.m.r. spectroscopy. Bacteriophage φ64 was shown to cleave the cognate K64 exopolysaccharide by a β-elimination process; the resulting hex-4-enuronic acid, present as a terminal group in the derived oligosaccharide was fully characterised by hydrogenation and g.l.c.-m.s. of acetylated products, and by detailed n.m.r. studies including long-range heteronuclear experiments. Finally the structure of the heptasaccharide repeating unit of the Klebsiella K71 capsular polysaccharide was established by spectroscopic analysis of the oligosaccharides derived by bacteriophage φ71 cleavage of the polymer; features of the proposed structure were confirmed by chemical degradation studies performed on the native polysaccharide. 2016-02-22T07:20:45Z 2016-02-22T07:20:45Z 1988 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/17186 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Polysaccharides
Oligosaccharides
Enterobacteriaceae
Organic Chemistry
Ravenscroft, Neil
Chemical and spectroscopic studies of the capsular polysaccharides of some Klebsiella serotypes
thesis_degree_str Doctoral
title Chemical and spectroscopic studies of the capsular polysaccharides of some Klebsiella serotypes
title_full Chemical and spectroscopic studies of the capsular polysaccharides of some Klebsiella serotypes
title_fullStr Chemical and spectroscopic studies of the capsular polysaccharides of some Klebsiella serotypes
title_full_unstemmed Chemical and spectroscopic studies of the capsular polysaccharides of some Klebsiella serotypes
title_short Chemical and spectroscopic studies of the capsular polysaccharides of some Klebsiella serotypes
title_sort chemical and spectroscopic studies of the capsular polysaccharides of some klebsiella serotypes
topic Polysaccharides
Oligosaccharides
Enterobacteriaceae
Organic Chemistry
url http://hdl.handle.net/11427/17186
work_keys_str_mv AT ravenscroftneil chemicalandspectroscopicstudiesofthecapsularpolysaccharidesofsomeklebsiellaserotypes