Affiliation:
1. Public Health Research Institute, 225 Warren St., Newark, New Jersey 07103
Abstract
ABSTRACT
Inhibition of DNA replication in an
Escherichia coli dnaB-22
mutant failed to block quinolone-mediated lethality. Inhibition of protein synthesis by chloramphenicol inhibited nalidixic acid lethality and, to a lesser extent, ciprofloxacin lethality in both
dnaB-22
and wild-type cells. Thus, major features of quinolone-mediated lethality do not depend on ongoing replication.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Reference26 articles.
1. Caruthers, J. M., and D. B. McKay. 2002. Helicase structure and mechanism. Curr. Opin. Struct. Biol.12:123-133.
2. Chen, C.-R., M. Malik, M. Snyder, and K. Drlica. 1996. DNA gyrase and topoisomerase IV on the bacterial chromosome: quinolone-induced DNA cleavage. J. Mol. Biol.258:627-637.
3. D'Arpa, P., C. Beardmore, and L. F. Liu. 1990. Involvement of nucleic acid synthesis in cell killing mechanisms of topoisomerase poisons. Cancer Res.50:6919-6924.
4. Mechanism of Action of Nalidixic Acid on
Escherichia coli
III. Conditions Required for Lethality
5. Drlica, K., and D. C. Hooper. 2003. Mechanisms of quinolone action, p. 19-40. In D. C. Hooper and E. Rubinstein (ed.), Quinolone antimicrobial agents, 3rd ed. American Society for Microbiology, Washington, D.C.
Cited by
25 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献