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Updated: Jul 30, 2026

Recombinant Protein Expression, Crystallization, and Biophysical Studies of a Bacillus-conserved Nucleotide Pyrophosphorylase, BcMazG
Published on: May 16, 2017
MazF-mediated cell death in Escherichia coli: a point of no return
Shahar Amitai1, Yussuf Yassin, Hanna Engelberg-Kulka
1Department of Molecular Biology, The Hebrew University-Hadassah Medical School, P.O. Box 12272, Jerusalem 91120, Israel.
Abstract:
mazEF is a stress-induced toxin-antitoxin module, located on the chromosome of Escherichia coli, that we have previously described to be responsible for programmed cell death in E. coli. mazF specifies a stable toxin, and mazE specifies a labile antitoxin. Recently, it was reported that inhibition of translation and cell growth by ectopic overexpression of the toxin MazF can be reversed by the action of the antitoxin MazE ectopically overexpressed at a later time. Based on these results, it was suggested that rather than inducing cell death, mazF induces a state of reversible bacteriostasis (K. Pederson, S. K. Christensen, and K. Gerdes, Mol. Microbiol. 45:501-510, 2002). Using a similar ectopic overexpression system, we show here that overexpression of MazE could reverse MazF lethality only over a short window of time. The size of that window depended on the nature of the medium in which MazF was overexpressed. Thus, we found "a point of no return," which occurred sooner in minimal M9 medium than it did in the rich Luria-Bertani medium. We also describe a state in which the effect of MazF on translation could be separated from its effect on cell death: MazE overproduction could completely reverse the inhibitory effect of MazF on translation, while not affecting the bacteriocidic effect of MazF at all. Our results reported here support our view that the mazEF module mediates cell death and is part of a programmed cell death network.
Insights
The mazEF toxin-antitoxin system in E. coli mediates programmed cell death. Its effects are irreversible after a certain point, even if translation inhibition is reversed.
Area of Science:
- Microbiology
- Molecular Biology
- Bacterial Genetics
Background:
- The mazEF system in Escherichia coli is a stress-induced toxin-antitoxin module.
- MazF is a stable toxin, and MazE is a labile antitoxin.
- Previous studies suggested mazEF induces reversible bacteriostasis.
Purpose of the Study:
- To investigate the reversibility of MazF-induced cell death by MazE.
- To determine the influence of growth medium on the MazF-MazE interaction.
- To differentiate MazF's effects on translation versus cell death.
Main Methods:
- Ectopic overexpression of MazF and MazE in E. coli.
- Growth curve analysis in different media (M9 minimal and Luria-Bertani rich).
- Assessment of translation inhibition and cell lethality.
Main Results:
- MazE could only reverse MazF lethality within a limited time window.
- This "point of no return" occurred faster in M9 medium than in LB medium.
- MazE reversed MazF's translational inhibition but not its cell-killing effect.
Conclusions:
- The mazEF module mediates irreversible cell death, not just reversible bacteriostasis.
- Environmental conditions significantly impact the mazEF system's outcome.
- Results support mazEF's role in programmed cell death networks.
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