Literature DB >> 15036322

Bacterial programmed cell death systems as targets for antibiotics.

Hanna Engelberg-Kulka1, Boaz Sat, Myriam Reches, Shahar Amitai, Ronen Hazan.   

Abstract

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.

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Year:  2004        PMID: 15036322     DOI: 10.1016/j.tim.2003.12.008

Source DB:  PubMed          Journal:  Trends Microbiol        ISSN: 0966-842X            Impact factor:   17.079


  75 in total

1.  Induction of Escherichia coli chromosomal mazEF by stressful conditions causes an irreversible loss of viability.

Authors:  Ilana Kolodkin-Gal; Hanna Engelberg-Kulka
Journal:  J Bacteriol       Date:  2006-05       Impact factor: 3.490

2.  Escherichia coli mazEF-mediated cell death is triggered by various stressful conditions.

Authors:  Ronen Hazan; Boaz Sat; Hanna Engelberg-Kulka
Journal:  J Bacteriol       Date:  2004-06       Impact factor: 3.490

Review 3.  Single-cell microbiology: tools, technologies, and applications.

Authors:  Byron F Brehm-Stecher; Eric A Johnson
Journal:  Microbiol Mol Biol Rev       Date:  2004-09       Impact factor: 11.056

4.  Detection of endogenous MazF enzymatic activity in Staphylococcus aureus.

Authors:  Julia J van Rensburg; Paul J Hergenrother
Journal:  Anal Biochem       Date:  2013-08-29       Impact factor: 3.365

5.  Crystallization of the C-terminal domain of the addiction antidote CcdA in complex with its toxin CcdB.

Authors:  Lieven Buts; Natalie De Jonge; Remy Loris; Lode Wyns; Minh-Hoa Dao-Thi
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2005-09-30

6.  The solution structure of ParD, the antidote of the ParDE toxin antitoxin module, provides the structural basis for DNA and toxin binding.

Authors:  Monika Oberer; Klaus Zangger; Karl Gruber; Walter Keller
Journal:  Protein Sci       Date:  2007-08       Impact factor: 6.725

7.  The extracellular death factor: physiological and genetic factors influencing its production and response in Escherichia coli.

Authors:  Ilana Kolodkin-Gal; Hanna Engelberg-Kulka
Journal:  J Bacteriol       Date:  2008-02-29       Impact factor: 3.490

8.  A continuous fluorometric assay for the assessment of MazF ribonuclease activity.

Authors:  Nora R Wang; Paul J Hergenrother
Journal:  Anal Biochem       Date:  2007-07-26       Impact factor: 3.365

9.  MazF-mediated cell death in Escherichia coli: a point of no return.

Authors:  Shahar Amitai; Yussuf Yassin; Hanna Engelberg-Kulka
Journal:  J Bacteriol       Date:  2004-12       Impact factor: 3.490

10.  The yefM-yoeB toxin-antitoxin systems of Escherichia coli and Streptococcus pneumoniae: functional and structural correlation.

Authors:  Concha Nieto; Izhack Cherny; Seok Kooi Khoo; Mario García de Lacoba; Wai Ting Chan; Chew Chieng Yeo; Ehud Gazit; Manuel Espinosa
Journal:  J Bacteriol       Date:  2006-10-27       Impact factor: 3.490

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