Related Experiment Video
Updated: Aug 11, 2026

The Use of a β-lactamase-based Conductimetric Biosensor Assay to Detect Biomolecular Interactions
Published on: February 1, 2018
CTX-M-type beta-lactamases: an emerging group of extended-spectrum enzymes
L S Tzouvelekis1, E Tzelepi, P T Tassios
1Department of Microbiology, Medical School, National University of Athens, M. Asias 75, Athens, Greece.
Abstract:
CTX-M-type beta-lactamases constitute a novel group of class A beta-lactamases with extended-spectrum properties. They are encoded by transferable plasmids and found in various enterobacteria, mostly Salmonella typhimurium, Escherichia coli, Klebsiella pneumoniae and Proteus mirabilis. CTX-M enzymes share extensive sequence similarity with the chromosomal beta-lactamases of Klebsiella oxytoca. They efficiently hydrolyze many newer broad-spectrum oximino-beta-lactams including cefotaxime, ceftriaxone and aztreonam and are readily inhibited by tazobactam and clavulanate. CTX-M-producing enterobacteria are endemic in Latin America and in some areas of North Eastern Europe. Data on their structure, properties and epidemiology are discussed.
Insights
CTX-M-type beta-lactamases are a new class of enzymes found in enterobacteria that hydrolyze broad-spectrum antibiotics. These enzymes, encoded by plasmids, are prevalent in Latin America and parts of Europe.
Area of Science:
- Microbiology
- Biochemistry
- Molecular Biology
Background:
- CTX-M-type beta-lactamases represent a novel group of class A beta-lactamases.
- These enzymes possess extended-spectrum hydrolytic properties.
Purpose of the Study:
- To discuss the structure, properties, and epidemiology of CTX-M enzymes.
- To highlight their significance in antibiotic resistance.
Main Methods:
- Comparative sequence analysis.
- Enzyme activity assays.
- Epidemiological surveillance data analysis.
Main Results:
- CTX-M enzymes efficiently hydrolyze broad-spectrum oximino-beta-lactams (e.g., cefotaxime, ceftriaxone, aztreonam).
- They are encoded by transferable plasmids and found in key enterobacteria (e.g., Salmonella typhimurium, Escherichia coli, Klebsiella pneumoniae).
- CTX-M enzymes show similarity to Klebsiella oxytoca chromosomal beta-lactamases and are inhibited by tazobactam and clavulanate.
Conclusions:
- CTX-M-producing enterobacteria are endemic in Latin America and parts of North Eastern Europe.
- Understanding CTX-M enzymes is crucial for combating antibiotic resistance.
More Related Videos
Related Concept Videos
Inducible Operons: lac Operon
Development of Antibiotic Resistance
Bacterial Toxins
Mechanism of Antibiotic Resistance in MRSA
Inhibitors of Gram-positive Cell Wall Synthesis
Clinical Significance of Antibiotic Resistance

