UWSpace is currently experiencing technical difficulties resulting from its recent migration to a new version of its software. These technical issues are not affecting the submission and browse features of the site. UWaterloo community members may continue submitting items to UWSpace. We apologize for the inconvenience, and are actively working to resolve these technical issues.
 

Experimental characterization of a catalytically active flagellin variant in Clostridium haemolyticum

dc.contributor.authorBandukwala, Hina
dc.date.accessioned2017-04-18T18:43:48Z
dc.date.available2018-08-17T04:50:12Z
dc.date.issued2017-04-18
dc.date.submitted2017-03-22
dc.description.abstractThe bacterial flagellum is made up of approximately 20,000 subunits of the monomeric protein, flagellin, and plays a role in cell motility and pathogenesis. The extreme sequence diversity within the hypervariable region of flagellin genes observed across phyla suggests hidden functional diversity. This thesis outlines the discovery of the first family of flagellin variants with proteolytic activity. A multi-faceted approach revealed a conserved HExxH motif within the hypervariable region (HVR) of these flagellin variants. The motif is characteristic of the Gluzincin family of thermolysin-like peptidases and was found to be conserved in 74 bacterial species spanning over 32 genera. Experimental validation began with the recombinant expression and purification of the HVR of the flagellin FliA(H) from the species Clostridium haemolyticum, an animal pathogen. An approach using mass spectrometry and proteomics revealed that the substrate specificity of this flagellin protease is similar to that of zinc-dependant matrix metallopeptidases (MMPs). Furthermore, peptide sequencing of harvested C.haemolyticum flagellar filaments revealed that the proteolytic flagellin was the second most dominant flagellin component and was also shown to have MMP-like protease activity. Considering the expanded functional repertoire of this organelle in the recent years, this flagellin-associated protease may play a role in chemotaxis, biofilm formation, adhesion and pathogenesis.en
dc.identifier.urihttp://hdl.handle.net/10012/11677
dc.language.isoenen
dc.pendingfalse
dc.publisherUniversity of Waterlooen
dc.subjectflagellinen
dc.subjectFliA(H)en
dc.subjectbacteria flagellaen
dc.subjectPICSen
dc.subjectstructural bioinformaticsen
dc.subjectprotease specificity profilingen
dc.subjectproteolysisen
dc.titleExperimental characterization of a catalytically active flagellin variant in Clostridium haemolyticumen
dc.typeMaster Thesisen
uws-etd.degreeMaster of Scienceen
uws-etd.degree.departmentBiologyen
uws-etd.degree.disciplineBiologyen
uws-etd.degree.grantorUniversity of Waterlooen
uws-etd.embargo.terms1 year 4 monthsen
uws.comment.hiddenSpecies names (Clostridium haemolyticum) needs to be italicizeden
uws.contributor.advisorDoxey, Andrew
uws.contributor.advisorCharles, Trevor
uws.contributor.affiliation1Faculty of Scienceen
uws.peerReviewStatusUnrevieweden
uws.published.cityWaterlooen
uws.published.countryCanadaen
uws.published.provinceOntarioen
uws.scholarLevelGraduateen
uws.typeOfResourceTexten

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Bandukwala_Hina.pdf
Size:
19.17 MB
Format:
Adobe Portable Document Format
Description:
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
6.17 KB
Format:
Item-specific license agreed upon to submission
Description:

Collections