Controlled expression and functional characterisation of SasG - a surface protein of Staphylococcus aureus
Citation:
Rebecca Corrigan, 'Controlled expression and functional characterisation of SasG - a surface protein of Staphylococcus aureus', [thesis], Trinity College (Dublin, Ireland). School of Genetics and Microbiology, 2009, pp 292Download Item:
Abstract:
Staphylococcus aureus colonises the moist squamous epithelium of the anterior
nares. One of the adhesins likely to be responsible is the S. aureus surface protein G
(SasG) which has sequence similarity with the proteins Pls (plasmin sensitive) of S.
aureus and Aap (accumulation associated protein) of S. epidermidis. Expression of SasG
by a laboratory strain of S. aureus could not be detected by Western immunoblotting. To
enable investigation of SasG, the gene was cloned into two expression vectors, the IPTG-inducible
pMUTIN4 and the tetracycline-inducible pALC2073 and was introduced into
S. aureus. The level of induction from pMUTIN4 was poor and while induction from
pALC2073 was strong, repression was leaky. Site-directed mutagenesis was utilised in
order to improve both vectors.
Author: Corrigan, Rebecca
Advisor:
Foster, TimQualification name:
Doctor of Philosophy (Ph.D.)Publisher:
Trinity College (Dublin, Ireland). School of Genetics and MicrobiologyNote:
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Microbiology, Ph.D., Ph.D. Trinity College Dublin.Metadata
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