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Studies on the Vibrio alginolyticus sucrose utilization system cloned into Escherichia coli

Bibliography: pages 143-154.

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Bibliographic Details
Main Author: Scholle, Renate Regina
Other Authors: Woods, David R
Format: Thesis
Language:English
Published: Department of Molecular and Cell Biology 2016
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access_status_str Open Access
author Scholle, Renate Regina
author2 Woods, David R
author_browse Scholle, Renate Regina
Woods, David R
author_facet Woods, David R
Scholle, Renate Regina
author_sort Scholle, Renate Regina
collection Thesis
description Bibliography: pages 143-154.
format Thesis
id oai:open.uct.ac.za:11427/21906
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:26.116Z
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 Molecular and Cell Biology
publisherStr Department of Molecular and Cell Biology
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/21906 Studies on the Vibrio alginolyticus sucrose utilization system cloned into Escherichia coli Scholle, Renate Regina Woods, David R Vibrio Escherichia coli Sucrose Bibliography: pages 143-154. This dissertation forms part of the study on the molecular biology of the aerobic, collagenolytic, halotolerant, gram-negative organism Vibrio alginolyticus. The cloning, expression and regulation of the v. alginolyticus sucrose utilization system in Escherichia coli is discussed and the results of a molecular analysis of the sucrase gene (scrA) are presented. The clone pVSlOO, containing a sucrose utilization system, was isolated from a genomic library of v. alginolyticus. Plasmid pVSlOO was mapped and the origin of its insert determined by Southern blotting and DNA hybridization. The number and sizes of the polypeptide products encoded by plasmid pVSlOO were determined by DNAdirected cell-free protein synthesis. The capsule, produced by transformed and untransformed E. coli JA221 cells, was shown to be independent of the presence of plasmid pVSlOO. The sucrase activity assay was optimized with respect to time, pH, temperature and salt requirements. 2016-09-25T16:47:13Z 2016-09-25T16:47:13Z 1989 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/21906 eng application/pdf Department of Molecular and Cell Biology Faculty of Science University of Cape Town
spellingShingle Vibrio
Escherichia coli
Sucrose
Scholle, Renate Regina
Studies on the Vibrio alginolyticus sucrose utilization system cloned into Escherichia coli
thesis_degree_str Doctoral
title Studies on the Vibrio alginolyticus sucrose utilization system cloned into Escherichia coli
title_full Studies on the Vibrio alginolyticus sucrose utilization system cloned into Escherichia coli
title_fullStr Studies on the Vibrio alginolyticus sucrose utilization system cloned into Escherichia coli
title_full_unstemmed Studies on the Vibrio alginolyticus sucrose utilization system cloned into Escherichia coli
title_short Studies on the Vibrio alginolyticus sucrose utilization system cloned into Escherichia coli
title_sort studies on the vibrio alginolyticus sucrose utilization system cloned into escherichia coli
topic Vibrio
Escherichia coli
Sucrose
url http://hdl.handle.net/11427/21906
work_keys_str_mv AT schollerenateregina studiesonthevibrioalginolyticussucroseutilizationsystemclonedintoescherichiacoli