4.5 Review

Bacterial replicases and related polymerases

Journal

CURRENT OPINION IN CHEMICAL BIOLOGY
Volume 15, Issue 5, Pages 587-594

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.cbpa.2011.07.018

Keywords

-

Funding

  1. National Institute of General Medical Sciences [RO1 GM060273]
  2. National Science Foundation [MCB-0919961]
  3. Direct For Biological Sciences
  4. Div Of Molecular and Cellular Bioscience [0919961] Funding Source: National Science Foundation

Ask authors/readers for more resources

Bacterial replicases are complex, tripartite replicative machines. They contain a polymerase, Pol III, a beta(2) processivity factor and a DnaX complex ATPase that loads beta(2) onto DNA and chaperones Pol III onto the newly loaded beta(2). Many bacteria encode both a full length tau and a shorter gamma form of DnaX by a variety of mechanisms. The polymerase catalytic subunit of Pol III, alpha, contains a PHP domain that not only binds to prototypical epsilon Mg2+-dependent exonuclease, but also contains a second Zn2+-dependent proofreading exonuclease, at least in some bacteria. Replication of the chromosomes of low GC Gram-positive bacteria require two Pol Ills, one of which, DnaE, appears to extend RNA primers a only short distance before handing the product off to the major replicase, PolC. Other bacteria encode a second Pol III (ImuC) that apparently replaces Pol V, required for induced mutagenesis in E. coli. Approaches that permit simultaneous biochemical screening of all components of complex bacterial replicases promise inhibitors of specific protein targets and reaction stages.

Authors

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

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available