Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294116
Title: Studies towards the development of a host:vector system for the genus Clostridium
Author: Brehm, John Karl
ISNI:       0000 0001 3478 3662
Awarding Body: University of Warwick
Current Institution: University of Warwick
Date of Award: 1989
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Abstract:
Clostridia are widely recognised as organisms of biotechnological importance. This potential, however, cannot be fully exploited until reliable methods have been developed for the transfer of genetic information into and between members of the genus. As with other Gram-positive bacteria, attempts to develop host:vector systems have focused on protoplast transformation procedures. This approach, however, has been hampered by the lack of suitable plasmid vectors. Studies have been initiated to construct such a vector. As a potential source of a clostridial replicon, the cryptic plasmid of C. butvricum NCIB 7423 (pCBlOl, 6.05 kb) has been examined. The complete nucleotide sequence of pCBlOl was determined and it's minimal replicon characterised together with the elucidation of some of the mechanisms involved in it's replication. The erythromycin resistance determinant (Emr) of the Grampositive R-factor pAM/3l was chosen as a selectable marker and the entire nucleotide sequence of this gene was determined. The Ferredoxin (Fd) gene of Clostridium pasteurianum was cloned and employed in the construction of an expression cartridge. The effectiveness of this cartridge in promoting the expression of heterologous genes was examined using a promoter-less xvlE gene. The conjugative Streptococcus faecalis plasmid pAM/Jl was used to mobilise vectors carrying the xvlE gene (under the transcriptional control of the Fd promoter) into Clostridium acetobutvlicum where the gene was expressed. This represents one of the first reports of directed gene expression in C. acetobutylicum.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.294116  DOI: Not available
Keywords: QR Microbiology ; TP Chemical technology
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