TY - JOUR
T1 - Programmed cell death in Escherichia coli
T2 - Some antibiotics can trigger mazEF lethality
AU - Sat, B.
AU - Hazan, R.
AU - Fisher, T.
AU - Khaner, H.
AU - Glaser, G.
AU - Engelberg-Kulka, H.
PY - 2001
Y1 - 2001
N2 - The discovery of toxin-antitoxin gene pairs (also called addiction modules) on extrachromosomal elements of Escherichia coli, and particularly the discovery of homologous modules on the bacterial chromosome, suggest that a potential for programmed cell death may be inherent in bacterial cultures. We have reported on the E. coli mazEF system, a regulatable addiction module located on the bacterial chromosome. MazF is a stable toxin and MazE is a labile antitoxin. Here we show that cell death mediated by the E. coli mazEF module can be triggered by several antibiotics (rifampicin, chloramphenicol, and spectinomycin) that are general inhibitors of transcription and/or translation. These antibiotics inhibit the continuous expression of the labile antitoxin MazE, and as a result, the stable toxin MazF causes cell death. Our results have implications for the possible mode(s) of action of this group of antibiotics.
AB - The discovery of toxin-antitoxin gene pairs (also called addiction modules) on extrachromosomal elements of Escherichia coli, and particularly the discovery of homologous modules on the bacterial chromosome, suggest that a potential for programmed cell death may be inherent in bacterial cultures. We have reported on the E. coli mazEF system, a regulatable addiction module located on the bacterial chromosome. MazF is a stable toxin and MazE is a labile antitoxin. Here we show that cell death mediated by the E. coli mazEF module can be triggered by several antibiotics (rifampicin, chloramphenicol, and spectinomycin) that are general inhibitors of transcription and/or translation. These antibiotics inhibit the continuous expression of the labile antitoxin MazE, and as a result, the stable toxin MazF causes cell death. Our results have implications for the possible mode(s) of action of this group of antibiotics.
UR - http://www.scopus.com/inward/record.url?scp=0035108209&partnerID=8YFLogxK
U2 - 10.1128/JB.183.6.2041-2045.2001
DO - 10.1128/JB.183.6.2041-2045.2001
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C2 - 11222603
AN - SCOPUS:0035108209
SN - 0021-9193
VL - 183
SP - 2041
EP - 2045
JO - Journal of Bacteriology
JF - Journal of Bacteriology
IS - 6
ER -