Persistent bacterial infections and persister cells
RA Fisher, B Gollan, S Helaine - Nature Reviews Microbiology, 2017 - nature.com
Many bacteria can infect and persist inside their hosts for long periods of time. This can be
due to immunosuppression of the host, immune evasion by the pathogen and/or ineffective …
due to immunosuppression of the host, immune evasion by the pathogen and/or ineffective …
DNA gyrase, topoisomerase IV, and the 4-quinolones
K Drlica, X Zhao - Microbiology and molecular biology reviews, 1997 - Am Soc Microbiol
For many years, DNA gyrase was thought to be responsible both for unlinking replicated
daughter chromosomes and for controlling negative superhelical tension in bacterial DNA …
daughter chromosomes and for controlling negative superhelical tension in bacterial DNA …
Meiosis-specific DNA double-strand breaks are catalyzed by Spo11, a member of a widely conserved protein family
S Keeney, CN Giroux, N Kleckner - Cell, 1997 - cell.com
Meiotic recombination in S. cerevisiae is initiated by double-strand breaks (DSBs). In certain
mutants, breaks accumulate with a covalently attached protein, suggesting that cleavage is …
mutants, breaks accumulate with a covalently attached protein, suggesting that cleavage is …
Toxin-antitoxin systems in bacterial growth arrest and persistence
Bacterial persister cells constitute a subpopulation of genetically identical, metabolically
slow-growing cells that are highly tolerant of antibiotics and other environmental stresses …
slow-growing cells that are highly tolerant of antibiotics and other environmental stresses …
Type II toxin-antitoxin systems: evolution and revolutions
Type II toxin-antitoxin (TA) systems are small genetic elements composed of a toxic protein
and its cognate antitoxin protein, the latter counteracting the toxicity of the former. While TA …
and its cognate antitoxin protein, the latter counteracting the toxicity of the former. While TA …
Prokaryotic toxin–antitoxin stress response loci
K Gerdes, SK Christensen… - Nature Reviews …, 2005 - nature.com
Although toxin–antitoxin gene cassettes were first found in plasmids, recent database
mining has shown that these loci are abundant in free-living prokaryotes, including many …
mining has shown that these loci are abundant in free-living prokaryotes, including many …
Bacterial topoisomerase inhibitors: quinolone and pyridone antibacterial agents
LA Mitscher - Chemical reviews, 2005 - ACS Publications
The quinolone anti-infective agents are of wholly synthetic origin and are not modeled
knowingly after any natural antibiotic. Several ring systems are or have been involved …
knowingly after any natural antibiotic. Several ring systems are or have been involved …
Exploiting bacterial DNA gyrase as a drug target: current state and perspectives
F Collin, S Karkare, A Maxwell - Applied microbiology and biotechnology, 2011 - Springer
DNA gyrase is a type II topoisomerase that can introduce negative supercoils into DNA at
the expense of ATP hydrolysis. It is essential in all bacteria but absent from higher …
the expense of ATP hydrolysis. It is essential in all bacteria but absent from higher …
MazF cleaves cellular mRNAs specifically at ACA to block protein synthesis in Escherichia coli
Y Zhang, J Zhang, KP Hoeflich, M Ikura, G Qing… - Molecular cell, 2003 - cell.com
Escherichia coli contains operons called" addiction modules," encoding toxin and antitoxin,
which are responsible for growth arrest and cell death. Here, we demonstrate that MazF …
which are responsible for growth arrest and cell death. Here, we demonstrate that MazF …
Gyrase inhibitors induce an oxidative damage cellular death pathway in Escherichia coli
DJ Dwyer, MA Kohanski, B Hayete… - Molecular systems …, 2007 - embopress.org
Modulation of bacterial chromosomal supercoiling is a function of DNA gyrase‐catalyzed
strand breakage and rejoining. This reaction is exploited by both antibiotic and proteic …
strand breakage and rejoining. This reaction is exploited by both antibiotic and proteic …