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A cluster of two serine transfer RNA genes from Clostridium acetobutylicum P262

Bibliography: pages 105-115.

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Main Author: Sealy, Victoria Rosamond
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 Sealy, Victoria Rosamond
author2 Woods, David R
author_browse Sealy, Victoria Rosamond
Woods, David R
author_facet Woods, David R
Sealy, Victoria Rosamond
author_sort Sealy, Victoria Rosamond
collection Thesis
description Bibliography: pages 105-115.
format Thesis
id oai:open.uct.ac.za:11427/21497
institution University of Cape Town (South Africa)
language eng
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
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source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/21497 A cluster of two serine transfer RNA genes from Clostridium acetobutylicum P262 Sealy, Victoria Rosamond Woods, David R Reid, Sharon J Molecular and Cell Biology Bibliography: pages 105-115. A cloning system, using metronidazole as a screening tool and E. coli FI9 as a selection host, was previously established to clone C. acetobutylicum P262 electron transport genes which may play a role in solvent metabolism in this bacterium. In theory, metronidazole would be reduced under anaerobic conditions to a cytotoxic intermediate by C. acetobutylicum P262 electron transport genes or reductive enzymes cloned into a recombinant plasmid. This intermediate would kill the host E. coli FI9. One C. acetobutylicum P262 clone, pMETIOB, was found to render the E. coli strain FI9 sensitive to metronidazole, under anaerobic conditions. A number of subclones of the 2.56kb C. acetobutylicum P262 insert DNA were generated in Bluescript pKS and pSK. A range of exonuclease III deletions of this C. acetobutylicum P262 insert DNA were also generated which were shown to lose the metronidazole sensitivity phenotype on progressive deletion of the insert DNA. In vitro and in vivo protein transcription/translation experiments failed to reveal a protein product that was related to the metronidazole sensitivity phenotype. DNA hybridization confrrmed that the insert DNA of pMETIOB hybridized to C. acetobutylicum P262 chromosomal DNA, but not to E. coli chromosomal DNA. The nucleotide sequence of a 933-bp fragment of the C. acetobutylicum P262 insert DNA was determined. 2016-08-24T12:54:12Z 2016-08-24T12:54:12Z 1994 Master Thesis Masters MSc http://hdl.handle.net/11427/21497 eng application/pdf Department of Molecular and Cell Biology Faculty of Science University of Cape Town
spellingShingle Molecular and Cell Biology
Sealy, Victoria Rosamond
A cluster of two serine transfer RNA genes from Clostridium acetobutylicum P262
thesis_degree_str Master's
title A cluster of two serine transfer RNA genes from Clostridium acetobutylicum P262
title_full A cluster of two serine transfer RNA genes from Clostridium acetobutylicum P262
title_fullStr A cluster of two serine transfer RNA genes from Clostridium acetobutylicum P262
title_full_unstemmed A cluster of two serine transfer RNA genes from Clostridium acetobutylicum P262
title_short A cluster of two serine transfer RNA genes from Clostridium acetobutylicum P262
title_sort cluster of two serine transfer rna genes from clostridium acetobutylicum p262
topic Molecular and Cell Biology
url http://hdl.handle.net/11427/21497
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