Canada Spends Logo

Explore our Budget 2026 analysis

Grant: Operating Grant

McMaster University

$594,915.00

Toward Designed Antibiotics: Mechanisms and Inhibition of PEP Utilizing Enzymes

FY 2010-11

Summary
Antibiotic resistance is a serious and rapidly escalating health care problem. We are faced with the prospect of growing numbers of pan-resistant bacteria - bacteria resistant to every known antibiotic. We study two types of enzymes that bacteria need to survive. The carboxyvinyl transferases synthesize the aromatic amino acids and components of the cell wall. The carboxyketose synthases are a group of three enzymes which produce unusual sugars that bacteria require. One sugar is a building block for aromatic compounds, another forms part of the bacterial cell's outer surface, and the third helps bacteria evade the immune system. We use a variety of techniques to gain a detailed understanding of the reactions catalyzed by our target enzymes, including determining the structures of the high-energy species by measuring kinetic isotope effects, determining reaction rates, determining the enzymes' structures, and designing and testing new enzyme inhibitors. Having a thorough understanding of how the enzymes work allows us to design new inhibitors. These inhibitors will have the potential to become new antibiotics to treat bacterial infections.
Program
Operating Grant
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
226166
Name
Berti Paul J
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Biochemistry & Molecular Biology - A
Projecttitle
Toward Designed Antibiotics: Mechanisms and Inhibition of PEP Utilizing Enzymes
Programtype2
Operating Grants
Orgnameinp2
McMaster University
Cihramount2
$594,915
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Bacterial Infection; Carboxyketose Synthase; Carboxyvinyl Transfer; Enzyme Inhibition; Enzyme Mechanisms; Inhibitor Design; Kinetic Isotope Effects; Protein Structure
Abstract
Antibiotic resistance is a serious and rapidly escalating health care problem. We are faced with the prospect of growing numbers of pan-resistant bacteria - bacteria resistant to every known antibiotic. We study two types of enzymes that bacteria need to survive. The carboxyvinyl transferases synthesize the aromatic amino acids and components of the cell wall. The carboxyketose synthases are a group of three enzymes which produce unusual sugars that bacteria require. One sugar is a building block for aromatic compounds, another forms part of the bacterial cell's outer surface, and the third helps bacteria evade the immune system. We use a variety of techniques to gain a detailed understanding of the reactions catalyzed by our target enzymes, including determining the structures of the high-energy species by measuring kinetic isotope effects, determining reaction rates, determining the enzymes' structures, and designing and testing new enzyme inhibitors. Having a thorough understanding of how the enzymes work allows us to design new inhibitors. These inhibitors will have the potential to become new antibiotics to treat bacterial infections.
Competitiondate
201103
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Berti, Paul J
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $594,915~ $0~
McMaster University - $594,915 Grant (2010-11) | Canada Spends