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Laboratory Variants GES G170L , GES G170K , and GES G170H Increase Carbapenem Hydrolysis and Confer Resistance to Clavulanic Acid
- Source :
- Antimicrobial Agents and Chemotherapy. 65
- Publication Year :
- 2021
- Publisher :
- American Society for Microbiology, 2021.
-
Abstract
- The Guiana extended-spectrum (GES) β-lactamase GES G170H , GES G170L , and GES G170K mutants showed k cat , K m , and k cat / K m values very dissimilar to those of GES-1 and GES-5. The enhancement of the hydrolytic activity against carbapenems is potentially due to a shift of the substrate in the active site that provides better positioning of the deacylating water molecule caused by the presence of the imidazole ring of H170 and of the long side chain of K170 and L170.
- Subjects :
- Carbapenem
Stereochemistry
beta-Lactamases
03 medical and health sciences
chemistry.chemical_compound
Hydrolysis
Clavulanic acid
medicine
Side chain
Imidazole
Pharmacology (medical)
Enzyme kinetics
B-lactamases
GES
In silico molecular modeling
Anti-Bacterial Agents
Clavulanic Acid
Carbapenems
Laboratories
030304 developmental biology
Pharmacology
0303 health sciences
biology
030306 microbiology
Active site
Substrate (chemistry)
Infectious Diseases
chemistry
biology.protein
medicine.drug
Subjects
Details
- ISSN :
- 10986596 and 00664804
- Volume :
- 65
- Database :
- OpenAIRE
- Journal :
- Antimicrobial Agents and Chemotherapy
- Accession number :
- edsair.doi.dedup.....ef3e4e75db6121b63facf36383fdeb18
- Full Text :
- https://doi.org/10.1128/aac.01931-20