Pyrophosphate release acts as a kinetic checkpoint during high-fidelity DNA replication by the Staphylococcus aureus replicative polymerase PolC. Issue 14 (24th July 2021)

• Record Type: Journal Article
• Authors: Fagan, Sean P; Mukherjee, Purba; Jaremko, William J; Nelson-Rigg, Rachel; Wilson, Ryan C; Dangerfield, Tyler L; Johnson, Kenneth A; Lahiri, Indrajit; Pata, Janice D
• Is Part Of: Nucleic acids research. Volume 49:Issue 14(2021)
• Page Start: 8324
• Page End: 8338
• Publication Date: 2021-07-24
• Subjects: Nucleic acids -- Periodicals; Molecular biology -- Periodicals; 572.805
• DOI: 10.1093/nar/gkab613
• Languages: English
• ISSNs: 0305-1048

Abstract

Abstract: Bacterial replication is a fast and accurate process, with the bulk of genome duplication being catalyzed by the α subunit of DNA polymerase III within the bacterial replisome. Structural and biochemical studies have elucidated the overall properties of these polymerases, including how they interact with other components of the replisome, but have only begun to define the enzymatic mechanism of nucleotide incorporation. Using transient-state methods, we have determined the kinetic mechanism of accurate replication by PolC, the replicative polymerase from the Gram-positive pathogen Staphylococcus aureus . Remarkably, PolC can recognize the presence of the next correct nucleotide prior to completing the addition of the current nucleotide. By modulating the rate of pyrophosphate byproduct release, PolC can tune the speed of DNA synthesis in response to the concentration of the next incoming nucleotide. The kinetic mechanism described here would allow PolC to perform high fidelity replication in response to diverse cellular environments.