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An investigation into the partition functions of the broad-host-range Plasmid pTF-FC2

The broad-host-range Thiobacillus ferrooxidans plasmid pTF-FC2 is stably inherited over many generations despite a low copy number. The pas genes which lie between the repB primase and the repA helicase encode a proteic plasmid stabilisation system and are capable of stabilising the unstable heterol...

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Main Author: Smith, Anthony S G
Other Authors: Rawlings, Doug
Format: Thesis
Language:English
Published: Department of Molecular and Cell Biology 2016
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access_status_str Open Access
author Smith, Anthony S G
author2 Rawlings, Doug
author_browse Rawlings, Doug
Smith, Anthony S G
author_facet Rawlings, Doug
Smith, Anthony S G
author_sort Smith, Anthony S G
collection Thesis
description The broad-host-range Thiobacillus ferrooxidans plasmid pTF-FC2 is stably inherited over many generations despite a low copy number. The pas genes which lie between the repB primase and the repA helicase encode a proteic plasmid stabilisation system and are capable of stabilising the unstable heterologous R1 replicon present on p0U82. The deletion of the pas genes has been shown not to change the copy number of mutant plasmids. This suggested that the pas genes are not involved in replication and function as a stabilisation cassette. The pasA gene encodes an antidote, the pasB gene a toxin which exerts a bacteriocidal effect in an E. coli host and the pasC gene a protein which moderates the toxic effect of PasB. The PasC is unique in proteic plasmid stabilisation systems and reduces PasB toxicity only in the presence of PasA. PasA is able to repress the pas promoter and the addition of PasB increases this repression. PasC has been shown not to effect the pas promoter by itself. In the presence of PasA and PasB, PasC reduces the ability of PasA and PasB to repress the pas promoter. PasC is thought to stabilise the interaction of PasA and PasB and in doing so reduces their ability to function as repressors of the pas operon. The IncQ plasmid RSF1010 which has similarity to pTF-FC2 has two genes in a position analogous to the pasA, pasB and pasC genes. These genes have been found to be unable to function as a plasmid stabilisation system.
format Thesis
id oai:open.uct.ac.za:11427/20455
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:40:54.708Z
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:11427/20455 An investigation into the partition functions of the broad-host-range Plasmid pTF-FC2 Smith, Anthony S G Rawlings, Doug Molecular and Cell Biology The broad-host-range Thiobacillus ferrooxidans plasmid pTF-FC2 is stably inherited over many generations despite a low copy number. The pas genes which lie between the repB primase and the repA helicase encode a proteic plasmid stabilisation system and are capable of stabilising the unstable heterologous R1 replicon present on p0U82. The deletion of the pas genes has been shown not to change the copy number of mutant plasmids. This suggested that the pas genes are not involved in replication and function as a stabilisation cassette. The pasA gene encodes an antidote, the pasB gene a toxin which exerts a bacteriocidal effect in an E. coli host and the pasC gene a protein which moderates the toxic effect of PasB. The PasC is unique in proteic plasmid stabilisation systems and reduces PasB toxicity only in the presence of PasA. PasA is able to repress the pas promoter and the addition of PasB increases this repression. PasC has been shown not to effect the pas promoter by itself. In the presence of PasA and PasB, PasC reduces the ability of PasA and PasB to repress the pas promoter. PasC is thought to stabilise the interaction of PasA and PasB and in doing so reduces their ability to function as repressors of the pas operon. The IncQ plasmid RSF1010 which has similarity to pTF-FC2 has two genes in a position analogous to the pasA, pasB and pasC genes. These genes have been found to be unable to function as a plasmid stabilisation system. 2016-07-19T14:20:52Z 2016-07-19T14:20:52Z 1997 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/20455 eng application/pdf Department of Molecular and Cell Biology Faculty of Science University of Cape Town
spellingShingle Molecular and Cell Biology
Smith, Anthony S G
An investigation into the partition functions of the broad-host-range Plasmid pTF-FC2
thesis_degree_str Doctoral
title An investigation into the partition functions of the broad-host-range Plasmid pTF-FC2
title_full An investigation into the partition functions of the broad-host-range Plasmid pTF-FC2
title_fullStr An investigation into the partition functions of the broad-host-range Plasmid pTF-FC2
title_full_unstemmed An investigation into the partition functions of the broad-host-range Plasmid pTF-FC2
title_short An investigation into the partition functions of the broad-host-range Plasmid pTF-FC2
title_sort investigation into the partition functions of the broad host range plasmid ptf fc2
topic Molecular and Cell Biology
url http://hdl.handle.net/11427/20455
work_keys_str_mv AT smithanthonysg aninvestigationintothepartitionfunctionsofthebroadhostrangeplasmidptffc2
AT smithanthonysg investigationintothepartitionfunctionsofthebroadhostrangeplasmidptffc2