Grant: CIHR Fellowship
Queen's University (Kingston, Ontario)
$135,000.00
Structural and Functional Analysis of virulence-associated Clostridium perfringens enzymes: Insights into bacterial pathogenesis
EF 2008-09
Résumé
Clostridium perfringens is a common bacterium, which is responsible for food poisoning and gas gangrene in humans. The infectious properties of this bacterium rely on the enzymes that it produces and secreted in to the extracellular environment. We will determine the structure of novel secreted enzyme and characterize its function in relation to its putative role in pathogenesis. In particular, we will look at how regions of the enzyme interact with host sugars and cells found in the human gut and tissue. The results from these studies will provide new insights into the function of this enzyme in C. perfringens viability and pathogenesis. Findings from this study may contribute to the future design of novel antimicrobial compounds.
Programme
CIHR Fellowship
Bénéficiaire
Emplacement
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
174285
Name
Kunjachen Jobby M
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Fellowships - Post-PhD
Projecttitle
Structural and Functional Analysis of virulence-associated Clostridium perfringens enzymes: Insights into bacterial pathogenesis
Programtype2
Fellowship Programs
Orgnameinp2
Queen's University (Kingston, Ontario)
Cihramount2
$135,000
Cihrequipment2
$0
Programname2
CIHR Fellowship
Keyworddelim
Bacterial Pathogenesis; Glycoside Hydrolases; Nmr Spectroscopy; Protein Ligand Interaction; Structural Biology; Toxins
Abstract
Clostridium perfringens is a common bacterium, which is responsible for food poisoning and gas gangrene in humans. The infectious properties of this bacterium rely on the enzymes that it produces and secreted in to the extracellular environment. We will determine the structure of novel secreted enzyme and characterize its function in relation to its putative role in pathogenesis. In particular, we will look at how regions of the enzyme interact with host sugars and cells found in the human gut and tissue. The results from these studies will provide new insights into the function of this enzyme in C. perfringens viability and pathogenesis. Findings from this study may contribute to the future design of novel antimicrobial compounds.
Competitiondate
200810
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Kunjachen, Jobby M
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $135,000~ $0~