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Journal of Bacteriology, July 2006, p. 4673-4680, Vol. 188, No. 13
0021-9193/06/$08.00+0     doi:10.1128/JB.00316-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Staphylococcus aureus Helicase but Not Escherichia coli Helicase Stimulates S. aureus Primase Activity and Maintains Initiation Specificity{dagger}

Scott A. Koepsell,1,2 Marilynn A. Larson,1,2 Mark A. Griep,2,3* and Steven H. Hinrichs1,2

Department of Microbiology and Pathology, University of Nebraska Medical Center, Omaha, Nebraska 68198-6495,1 University of Nebraska Center for Biosecurity, Omaha, Nebraska 68198-6495,2 Department of Chemistry, University of Nebraska—Lincoln, Lincoln, Nebraska 68588-03043

Received 3 March 2006/ Accepted 17 April 2006

Bacterial primases are essential for DNA replication due to their role in polymerizing the formation of short RNA primers repeatedly on the lagging-strand template and at least once on the leading-strand template. The ability of recombinant Staphylococcus aureus DnaG primase to utilize different single-stranded DNA templates was tested using oligonucleotides of the sequence 5'-CAGA (CA)5 XYZ (CA)3-3', where XYZ represented the variable trinucleotide. These experiments demonstrated that S. aureus primase synthesized RNA primers predominately on templates containing 5'-d(CTA)-3' or TTA and to a much lesser degree on GTA-containing templates, in contrast to results seen with the Escherichia coli DnaG primase recognition sequence 5'-d(CTG)-3'. Primer synthesis was initiated complementarily to the middle nucleotide of the recognition sequence, while the third nucleotide, an adenosine, was required to support primer synthesis but was not copied into the RNA primer. The replicative helicases from both S. aureus and E. coli were tested for their ability to stimulate either S. aureus or E. coli primase. Results showed that each bacterial helicase could only stimulate the cognate bacterial primase. In addition, S. aureus helicase stimulated the production of full-length primers, whereas E. coli helicase increased the synthesis of only short RNA polymers. These studies identified important differences between E. coli and S. aureus related to DNA replication and suggest that each bacterial primase and helicase may have adapted unique properties optimized for replication.

* Corresponding author. Mailing address: Department of Chemistry, University of Nebraska—Lincoln, Hamilton Hall 614, Lincoln, NE 68588-0304. Phone: (402) 472-3429. Fax: (402) 472-9402. E-mail: mgriep1{at}unl.edu.

{dagger} Supplemental material for this article may be found at http://jb.asm.org/.

Journal of Bacteriology, July 2006, p. 4673-4680, Vol. 188, No. 13
0021-9193/06/$08.00+0     doi:10.1128/JB.00316-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Larson, M. A., Bressani, R., Sayood, K., Corn, J. E., Berger, J. M., Griep, M. A., Hinrichs, S. H. (2008). Hyperthermophilic Aquifex aeolicus initiates primer synthesis on a limited set of trinucleotides comprised of cytosines and guanines. Nucleic Acids Res 36: 5260-5269 [Abstract] [Full Text]  


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