scholarly journals A Major Portion of DNA Gyrase Inhibitor Microcin B17 Undergoes anN,O-Peptidyl Shift during Synthesis

2011 ◽  
Vol 286 (30) ◽  
pp. 26308-26318 ◽  
Author(s):  
Dmitry Ghilarov ◽  
Marina Serebryakova ◽  
Irina Shkundina ◽  
Konstantin Severinov
2001 ◽  
Vol 98 (14) ◽  
pp. 7712-7717 ◽  
Author(s):  
D. B. Zamble ◽  
D. A. Miller ◽  
J. G. Heddle ◽  
A. Maxwell ◽  
C. T. Walsh ◽  
...  

2019 ◽  
Vol 73 (4) ◽  
pp. 749-762.e5 ◽  
Author(s):  
Dmitry Ghilarov ◽  
Clare E.M. Stevenson ◽  
Dmitrii Y. Travin ◽  
Julia Piskunova ◽  
Marina Serebryakova ◽  
...  

1994 ◽  
Vol 91 (10) ◽  
pp. 4519-4523 ◽  
Author(s):  
P. Yorgey ◽  
J. Lee ◽  
J. Kordel ◽  
E. Vivas ◽  
P. Warner ◽  
...  

2015 ◽  
Vol 59 (11) ◽  
pp. 6689-6695 ◽  
Author(s):  
George A. Jacoby ◽  
Marian A. Corcoran ◽  
David C. Hooper

ABSTRACTQnr is a plasmid-encoded and chromosomally determined protein that protects DNA gyrase and topoisomerase IV from inhibition by quinolones. Despite its prevalence worldwide and existence prior to the discovery of quinolones, its native function is not known. Other synthetic compounds and natural products also target bacterial topoisomerases. A number were studied as molecular probes to gain insight into how Qnr acts. Qnr blocked inhibition by synthetic compounds with somewhat quinolone-like structure that target the GyrA subunit, such as the 2-pyridone ABT-719, the quinazoline-2,4-dione PD 0305970, and the spiropyrimidinetrione pyrazinyl-alkynyl-tetrahydroquinoline (PAT), indicating that Qnr is not strictly quinolone specific, but Qnr did not protect against GyrA-targeting simocyclinone D8 despite evidence that both simocyclinone D8 and Qnr affect DNA binding to gyrase. Qnr did not affect the activity of tricyclic pyrimidoindole or pyrazolopyridones, synthetic inhibitors of the GyrB subunit, or nonsynthetic GyrB inhibitors, such as coumermycin A1, novobiocin, gyramide A, or microcin B17.Thus, in this set of compounds the protective activity of Qnr was confined to those that, like quinolones, trap gyrase on DNA in cleaved complexes.


2003 ◽  
Vol 47 (2) ◽  
pp. 559-562 ◽  
Author(s):  
George A. Jacoby ◽  
Nancy Chow ◽  
Ken B. Waites

ABSTRACT Quinolone resistance encoded by the qnr gene and mediated by plasmid pMG252 was discovered in a clinical strain of Klebsiella pneumoniae that was isolated in 1994 at the University of Alabama at Birmingham Medical Center. The gene codes for a protein that protects DNA gyrase from quinolone inhibition and that belongs to the pentapeptide repeat family of proteins. The prevalence of the gene has been investigated by using PCR with qnr-specific primers with a sample of more than 350 gram-negative strains that originated in 18 countries and 24 states in the United States and that included many strains with plasmid-mediated AmpC or extended spectrum β-lactamase enzymes. qnr was found in isolates from the University of Alabama at Birmingham only during 6 months in 1994, despite the persistence of the gene for FOX-5 β-lactamase, which is linked to qnr on pMG252. Isolates from other locations were negative for qnr. The prevalence of mcbG in the same sample was also examined. mcbG encodes another member of the pentapeptide repeat family and is involved in immunity to microcin B17, which, like quinolones, targets DNA gyrase. A single clinical isolate contained mcbG on a transmissible R plasmid. This plasmid and one carrying the complete microcin B17 operon slightly decreased sparfloxacin susceptibility but had a much less protective effect than pMG252. Plasmid-mediated quinolone resistance was thus rare in the sample examined.


1991 ◽  
Vol 10 (2) ◽  
pp. 467-476 ◽  
Author(s):  
J. L. Vizán ◽  
C. Hernández-Chico ◽  
I. del Castillo ◽  
F. Moreno

Biochimie ◽  
2007 ◽  
Vol 89 (4) ◽  
pp. 500-507 ◽  
Author(s):  
William M. Parks ◽  
Andrew R. Bottrill ◽  
Olivier A. Pierrat ◽  
Marcus C. Durrant ◽  
Anthony Maxwell

1997 ◽  
Vol 23 (1) ◽  
pp. 161-168 ◽  
Author(s):  
Lara L. Madison ◽  
Eugenio I. Vivas ◽  
Yue‐Ming Li ◽  
Christopher T. Walsh ◽  
Roberto Kolter

Sign in / Sign up

Export Citation Format

Share Document