Abstract
The Bacillus plasmid pLS11 partitions faithfully during cell division. Using a partition-deficient plasmid vector, we randomly cloned DNA fragments of plasmid pLS11 and identified the locus that regulates plasmid partition (par) by cis complementation in Bacillus subtilis. The cloned par gene conferred upon the vector plasmid a high degree of segregational stability. The par locus was mapped to a 167-base-pair segment on pLS11, and its nucleotide sequence was determined. The cloned par fragment regulated the partition of several different Bacillus replicons, and it only functioned in cis; it did not contain the replication function nor elevate the plasmid copy number in B. subtilis. The expression of par was orientation specific with respect to the replication origin on the same plasmid. We propose that the pLS11-derived par functions as a single-stranded site that interacts with other components involved in plasmid partition during cell division.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Reference35 articles.
1. Requirements for transformation in Bacillus subtilis;Anagnostopoulos C.;J. Bacteriol.,1961
2. Partition of unit-copy miniplasmids to daughter cells. I. P1 and F miniplasmids contain discrete, interchangeable sequences sufficient to promote equipartition;Austin S.;J. Mol. Biol.,1983
3. Partition of unit-copy miniplasmids to daughter cells. II. The partition region of miniplasmid P1 encodes an essential protein and a centromere-like site at which it acts;Austin S.;J. Mol. Biol.,1983
4. Two mini-F-encoded proteins are essential for equipartition;Austin S.;Plasmid,1983
5. A novel role for site-specific recombination in maintenance of bacterial replicons;Austin S.;Cell,1981
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