4.6 Review

The Macromolecular Machines that Duplicate the Escherichia coli Chromosome as Targets for Drug Discovery

Journal

ANTIBIOTICS-BASEL
Volume 7, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/antibiotics7010023

Keywords

DNA replication; Escherichia coli; inhibitors; replisome; replication fork; initiation; replication origin; DnaA; DnaB; DnaC; primase; DnaG; SSB; DNA gyrase; topoisomerase IV; DNA polymerase I; DNA polymerase III holoenzyme; sliding clamp; clamp loader; DNA ligase

Funding

  1. United States Department of Agriculture National Institute of Food and Agriculture, Hatch project [MICL02370]

Ask authors/readers for more resources

DNA replication is an essential process. Although the fundamental strategies to duplicate chromosomes are similar in all free-living organisms, the enzymes of the three domains of life that perform similar functions in DNA replication differ in amino acid sequence and their three-dimensional structures. Moreover, the respective proteins generally utilize different enzymatic mechanisms. Hence, the replication proteins that are highly conserved among bacterial species are attractive targets to develop novel antibiotics as the compounds are unlikely to demonstrate off-target effects. For those proteins that differ among bacteria, compounds that are species-specific may be found. Escherichia coli has been developed as a model system to study DNA replication, serving as a benchmark for comparison. This review summarizes the functions of individual E. coli proteins, and the compounds that inhibit them.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available