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Originally published In Press as doi:10.1074/jbc.M000552200 on April 3, 2000

J. Biol. Chem., Vol. 275, Issue 24, 18454-18461, June 16, 2000
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Interactions of DnaA Proteins from Distantly Related Bacteria with the Replication Origin of the Broad Host Range Plasmid RK2*

Ron CaspiDagger , Donald R. HelinskiDagger §, Marcin Pacek, and Igor Konieczny||

From the Dagger  Department of Biology, University of California, San Diego, La Jolla, California 92093-0322 and the  Department of Molecular and Cellular Biology, Faculty of Biotechnology, University of Gdansk, Gdansk, Poland

Replication initiation of the broad host range plasmid RK2 requires binding of the host-encoded DnaA protein to specific sequences (DnaA boxes) at its replication origin (oriV). In contrast to a chromosomal replication origin, which functionally interacts only with the native DnaA protein of the organism, the ability of RK2 to replicate in a wide range of Gram-negative bacterial hosts requires the interaction of oriV with many different DnaA proteins. In this study we compared the interactions of oriV with five different DnaA proteins. DNase I footprint, gel mobility shift, and surface plasmon resonance analyses showed that the DnaA proteins from Escherichia coli, Pseudomonas putida, and Pseudomonas aeruginosa bind to the DnaA boxes at oriV and are capable of inducing open complex formation, the first step in the replication initiation process. However, DnaA proteins from two Gram-positive bacteria, Bacillus subtilis and Streptomyces lividans, while capable of specifically interacting with the DnaA box sequences at oriV, do not bind stably and fail to induce open complex formation. These results suggest that the inability of the DnaA protein of a host bacterium to form a stable and functional complex with the DnaA boxes at oriV is a limiting step for plasmid host range.


* This work was supported in part by National Institutes of Health Research Grant AI-07194.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EMBL Data Bank with accession number(s) AF229442.

§ To whom correspondence should be addressed: Dept. of Biology, University of California, San Diego, 9500 Gilman Dr., La Jolla, CA 92093-0322. Tel.: 858-534-3638; Fax: 858-534-0559; E-mail: dhelinski@ucsd.edu.

|| Supported by MEN/NIH Research Grant 98-349 from the United States-Polish Maria Sklodowska Curie Fund II and by Polish State Committee for Scientific Research Grant 6P04A01115.


Copyright © 2000 by The American Society for Biochemistry and Molecular Biology, Inc.
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