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J. Biol. Chem., Vol. 275, Issue 24, 18454-18461, June 16, 2000
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,
§,
From the 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.
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
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.
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