نتایج جستجو برای: dna gyrase

تعداد نتایج: 507565  

Journal: :Antimicrobial agents and chemotherapy 1989
M E Cullen A W Wyke R Kuroda L M Fisher

Nalidixic acid, enoxacin, and other antibacterial 4-quinolones inhibit DNA gyrase activity by interrupting DNA breakage and reunion by A subunits of the A2B2 gyrase complex. Despite their clinical importance, the mode of quinolone action and mechanisms of resistance are poorly understood at the molecular level. Using a DNA fragment enrichment procedure, we isolated the gyrA gene from a uropatho...

2009
Anna Valenti Giuseppe Perugino Takehiko Nohmi Mosè Rossi Maria Ciaramella

Reverse gyrase is a unique DNA topoisomerase endowed with ATP-dependent positive supercoiling activity. It is typical of microorganisms living at high temperature and might play a role in maintenance of genome stability and repair. We have identified the translesion DNA polymerase SsoPolY/Dpo4 as one partner of reverse gyrase in the hyperthermophilic archaeon Sulfolobus solfataricus. We show he...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2001
D B Zamble D A Miller J G Heddle A Maxwell C T Walsh F Hollfelder

Microcin B17 (MccB17) is a 3.1-kDa Escherichia coli antibiotic that contains thiazole and oxazole heterocycles in a peptide backbone. MccB17 inhibits its cellular target, DNA gyrase, by trapping the enzyme in a complex that is covalently bound to double-strand cleaved DNA, in a manner similar to the well-known quinolone drugs. The identification of gyrase as the target of MccB17 provides an opp...

Journal: :RSC medicinal chemistry 2023

Fluoroquinolones are broad-spectrum antibiotics that target gyrase and topoisomerase IV, involved in DNA compaction segregation. We synthesized 28 novel norfloxacin hydroxamic acid derivatives with additional metal-chelating hydrophobic pharmacophores,...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2002
John H Tran George A Jacoby

Quinolones are potent antibacterial agents that specifically target bacterial DNA gyrase and topoisomerase IV. Widespread use of these agents has contributed to the rise of bacterial quinolone resistance. Previous studies have shown that quinolone resistance arises by mutations in chromosomal genes. Recently, a multiresistance plasmid was discovered that encodes transferable resistance to quino...

2017
Scott S Walker Marc Labroli Ronald E Painter Judyann Wiltsie Brad Sherborne Nicholas Murgolo Xinwei Sher Paul Mann Paul Zuck Charles G Garlisi Jing Su Stacia Kargman Li Xiao Giovanna Scapin Scott Salowe Kristine Devito Payal Sheth Nichole Buist Christopher M Tan Todd A Black Terry Roemer

To combat the threat of antibiotic-resistant Gram-negative bacteria, novel agents that circumvent established resistance mechanisms are urgently needed. Our approach was to focus first on identifying bioactive small molecules followed by chemical lead prioritization and target identification. Within this annotated library of bioactives, we identified a small molecule with activity against efflu...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1988
Y Yang G F Ames

A family of repetitive extragenic palindromic (REP) sequences is composed of hundreds of copies distributed throughout the chromosome. Their palindromic nature and conservation suggested that they are specifically recognized by a protein(s). We have identified DNA gyrase [DNA topoisomerase (ATP-hydrolysing), EC 5.99.1.3] as one of the REP-binding proteins. Gyrase has at least a 10-fold higher a...

Journal: :Antimicrobial agents and chemotherapy 2005
Ruth H Flatman Alison J Howells Lutz Heide Hans-Peter Fiedler Anthony Maxwell

We have characterized the interaction of a new class of antibiotics, simocyclinones, with bacterial DNA gyrase. Even though their structures include an aminocoumarin moiety, a key feature of novobiocin, coumermycin A(1), and clorobiocin, which also target gyrase, simocyclinones behave strikingly differently from these compounds. Simocyclinone D8 is a potent inhibitor of gyrase supercoiling, wit...

Journal: :Journal of Biological Chemistry 2014

Journal: :Nucleic acids research 2004
Martin Kampmann Daniela Stock

Hyperthermophilic organisms must protect their constituent macromolecules from heat-induced degradation. A general mechanism for thermoprotection of DNA in active cells is unknown. We show that reverse gyrase, the only protein that is both specific and common to all hyperthermophiles, reduces the rate of double-stranded DNA breakage approximately 8-fold at 90 degrees C. This activity does not r...

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