Bacterial programmed cell death systems as targets for antibiotics

被引:141
作者
Engelberg-Kulka, H [1 ]
Sat, B [1 ]
Reches, M [1 ]
Amitai, S [1 ]
Hazan, R [1 ]
机构
[1] Hebrew Univ Hadassah Med Sch, Dept Mol Biol, IL-91120 Jerusalem, Israel
基金
以色列科学基金会;
关键词
D O I
10.1016/j.tim.2003.12.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Growing experimental evidence has revealed the existence of programmed cell death (PCD) systems in bacteria. Among these is the mazEF system, which is a regulable suicide module located on the chromosome of E coli and of some other bacteria, including pathogens. Several well-known antibiotics have recently been found to cause cell death in E. coli by indirectly activating this built-in suicide module. These antibiotics belong to two groups: (i) inhibitors of transcription and/or translation; and (ii) inhibitors of folic acid metabolism resulting in thymine starvation. These data, together with the recent elucidation of the crystal structure of mazEF-directed components, hold promise for a rational chemical design of a new class of antibiotics that directly activate chromosomal suicide modules by interacting with their components. Because multi-drug resistance among bacterial pathogens is becoming more widespread, the results obtained might be useful as a basis for producing alternative drugs.
引用
收藏
页码:66 / 71
页数:6
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