Canada Spends Logo

Explorez notre analyse du budget 2026

Grant: Discovery Grants Program - Individual

University of Manitoba

$90,000.00

Structural determinants of the oxidative stress response

EF 2008-09

Résumé
The primary goal of the proposed research is to characterize proteins that protect organisms against oxidative stress. For over 20 years, research in the Loewen laboratory has been focused on monofunctional catalases and bifunctional catalase-peroxidases which have as their main physiological role the degradation of potentially toxic hydrogen peroxide to harmless water and oxygen. Work has progressed from bacterial genetic analysis, through molecular genetic characterization to protein structure determination and has provided a greatly improved understanding of how the enzymes respond to physiological challenge in different organisms. The recent adoption of protein X-ray crystallography procedures in the laboratory has made it possible to address questions about the catalytic mechanisms operating in the enzymes; the proposed research will continue in this direction. The goal of the proposed research is to characterize factors that protect organisms against hydrogen peroxide and the specific objectives are to characterize and rationalize structural features that affect the catalytic mechanisms in catalase-peroxidases and monofunctional catalases. The bifunctional catalase-peroxidases have gained considerable notoriety from their role as the activator of the widely used anti-tubercular pro-drug isoniazid. In particular, strains of M. tuberculosis lacking the enzyme are resistant to the drug, giving rise to the most common cause of the spread of isoniazid-resistant tuberculosis and producing a serious health risk. One branch of the proposed research will focus on defining the catalytic mechanism involved in isoniazid activation. The research will enhance our knowledge of enzyme catalysis by providing a better understanding of the mechanisms of hydrogen peroxide degradation and of isoniazid activation as a drug against tuberculosis.
Programme
Discovery Grants Program - Individual
Emplacement
Manitoba, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
9600-2007
Name nom
Loewen, Peter
Department département
Microbiology
Organization id
19
Institution établissement
University of Manitoba
Province en
Manitoba
Province fr
Manitoba
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2008
Competition year année de concours
2007
Award amount
90000
Program id
RGPIN
Program nane en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
32
Committee name en
Cell Biology
Committee name fr
Biologie cellulaire
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
Research subject code
5404
Research subject group en
Biochemistry
Research subject group fr
Biochimie
Research subject en
Enzymes
Research subject fr
Enzymes
Partie
2
Nb partie
5
Application title
Structural determinants of the oxidative stress response
Keyword
NA
Application summary
The primary goal of the proposed research is to characterize proteins that protect organisms against oxidative stress. For over 20 years, research in the Loewen laboratory has been focused on monofunctional catalases and bifunctional catalase-peroxidases which have as their main physiological role the degradation of potentially toxic hydrogen peroxide to harmless water and oxygen. Work has progressed from bacterial genetic analysis, through molecular genetic characterization to protein structure determination and has provided a greatly improved understanding of how the enzymes respond to physiological challenge in different organisms. The recent adoption of protein X-ray crystallography procedures in the laboratory has made it possible to address questions about the catalytic mechanisms operating in the enzymes; the proposed research will continue in this direction. The goal of the proposed research is to characterize factors that protect organisms against hydrogen peroxide and the specific objectives are to characterize and rationalize structural features that affect the catalytic mechanisms in catalase-peroxidases and monofunctional catalases. The bifunctional catalase-peroxidases have gained considerable notoriety from their role as the activator of the widely used anti-tubercular pro-drug isoniazid. In particular, strains of M. tuberculosis lacking the enzyme are resistant to the drug, giving rise to the most common cause of the spread of isoniazid-resistant tuberculosis and producing a serious health risk. One branch of the proposed research will focus on defining the catalytic mechanism involved in isoniazid activation. The research will enhance our knowledge of enzyme catalysis by providing a better understanding of the mechanisms of hydrogen peroxide degradation and of isoniazid activation as a drug against tuberculosis.