Abstract

DNA polymerase III (Pol III) is the replicative enzyme in bacteria. It consists of three subcomplexes, the catalytic core, the β clamp, and the clamp loader. While this complex has been thoroughly characterized in the model organism Escherichia coli, much less is known about its functioning and/or its specific properties in other bacteria. Biochemical studies highlighted specific features in the clamp loader subunit ψ of Pseudomonas aeruginosa as compared to its E. coli counterpart, and transposon mutagenesis projects identified the ψ-encoding gene holD among the strictly essential core genes of P. aeruginosa. By generating a P. aeruginosa holD conditional mutant, here we demonstrate that, as previously observed for E. coli holD mutants, HolD-depleted P. aeruginosa cells show strongly decreased growth, induction of the SOS response, and emergence of suppressor mutants at high frequency. However, differently from what was observed in E. coli, the growth of P. aeruginosa cells lacking HolD cannot be rescued by the deletion of genes for specialized DNA polymerases. We also observed that the residual growth of HolD-depleted cells is strictly dependent on homologous recombination functions, suggesting that recombination-mediated rescue of stalled replication forks is crucial to support replication by a ψ-deficient Pol III enzyme in P. aeruginosa.

Highlights

  • The Polymerase III (Pol III) enzyme is endowed with important properties that are required for efficient DNA replication, including a rapid elongation rate, high processivity, and tolerance to physiological salt concentrations [4,5]

  • Bacteria were cultured in Lysogeny Broth, Lennox formulation (LB; Acumedia, Neogen, Milan, Italy) for genetic manipulation, while growth assays were performed in Mueller–Hinton broth (MH; Difco, Becton Dickinson, Milan, Italy)

  • While the coding sequence of holD in PAO1 and other P. aeruginosa strains is annotated as a 702-bp sequence, encoding a 233-aa polypeptide, Jarvis and co-workers have demonstrated that the ψ subunit of the P. aeruginosa Pol III that is functional in vitro is 278-aa long, deriving from a translational start site located 135 nt upstream of the annotated one for PA4679 [13] (Figure S1)

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Summary

Introduction

Bacteria can replicate DNA at very high speed and with remarkable fidelity, through the activity of a complex protein machinery named replisome [1,2,3]. This machinery consists of a helicase (DnaB), a primase (DnaG), single-stranded DNA binding protein (SSB), and the DNA Polymerase III (Pol III) holoenzyme, known as replicase, which is the main replicative DNA polymerase in bacterial cells. The Pol III enzyme is endowed with important properties that are required for efficient DNA replication, including a rapid elongation rate, high processivity, and tolerance to physiological salt concentrations [4,5]

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