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Gene cloning studies in two nocardioform bacteria

Bibliography: pages 147-177.

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Bibliographic Details
Main Author: Hill, Russell
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 Hill, Russell
author2 Woods, David R
author_browse Hill, Russell
Woods, David R
author_facet Woods, David R
Hill, Russell
author_sort Hill, Russell
collection Thesis
description Bibliography: pages 147-177.
format Thesis
id oai:open.uct.ac.za:11427/21896
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:31:34.243Z
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:11427/21896 Gene cloning studies in two nocardioform bacteria Hill, Russell Woods, David R Actinomycetales Bacterial genetics Bibliography: pages 147-177. Nocardioforms are Gram-positive, aerobic actinomycetes and are a metabolically diverse group which produce antibiotics, useful enzymes, are important in the biotransformation of organic compounds and the decomposition of organic wastes and are important medically. A gene cloning vector designated pLR591 was constructed from the broad host range, multicopy Streptomyces plasmid pIJ702 and the positive selection Escherichia coli plasmid pEcoR251. This plasmid has useful features for the construction of actinomycete genomic libraries. Cloning of DNA into the unique Bg1II endonuclease site of pLR591 inactivated the lethal EcoRI gene derived from pEcoR251, thereby selecting for recombinant plasmids containing inserted DNA. The thiostrepton resistance gene derived from pIJ702 was shown to be functional in Streptomyces lividans enabling selection of recombinant pLR591 plasmids containing foreign DNA in S. lividans. The vector pLR591 therefore functions as a positive selection Streptomyces-E. coli shuttle vector facilitating construction of actinomycete genomic libraries in E. coli and subsequent transfer of recombinant plasmids into S. lividans. 2016-09-25T16:46:55Z 2016-09-25T16:46:55Z 1988 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/21896 eng application/pdf Department of Molecular and Cell Biology Faculty of Science University of Cape Town
spellingShingle Actinomycetales
Bacterial genetics
Hill, Russell
Gene cloning studies in two nocardioform bacteria
thesis_degree_str Doctoral
title Gene cloning studies in two nocardioform bacteria
title_full Gene cloning studies in two nocardioform bacteria
title_fullStr Gene cloning studies in two nocardioform bacteria
title_full_unstemmed Gene cloning studies in two nocardioform bacteria
title_short Gene cloning studies in two nocardioform bacteria
title_sort gene cloning studies in two nocardioform bacteria
topic Actinomycetales
Bacterial genetics
url http://hdl.handle.net/11427/21896
work_keys_str_mv AT hillrussell genecloningstudiesintwonocardioformbacteria