Identification of components of a new stability system of plasmid R1, ParD, that is close to the origin of replication of this plasmid
- 1 November 1987
- journal article
- research article
- Published by Springer Nature in Molecular Genetics and Genomics
- Vol. 210 (1) , 101-110
- https://doi.org/10.1007/bf00337764
Abstract
We provide evidence that a mutation which derepresses an autoregulated system that is located in the vicinity of the basic replicon of R1, stabilizes the ParA- and ParB- miniplasmid of R1 pKN1562, without increasing its copy number. The system, which we have called ParD, maps inside the 1.45-kb PstI-EcoRI fragment that is adjacent to the origin of replication of the plasmid. Two protiens whose expression is coordinated are components of the system. The sequence of the PstI-EcoRI fragment was obtained. The wild-type ParD system determines in cis a basal but detectable stability.Keywords
This publication has 54 references indexed in Scilit:
- Regulation of IncFII plasmid DNA replicationJournal of Molecular Biology, 1986
- Partitioning of plasmid R1Journal of Molecular Biology, 1986
- DNA replication of the resistance plasmid R100 and its controlAdvances in Biophysics, 1986
- Partition of unit-copy miniplasmids to daughter cellsJournal of Molecular Biology, 1983
- Prediction of the Secondary Structure of Proteins from their Amino Acid SequencePublished by Wiley ,1979
- Analysis of the accuracy and implications of simple methods for predicting the secondary structure of globular proteinsJournal of Molecular Biology, 1978
- Cell length, cell growth and cell divisionNature, 1976
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970
- Mutant Drug Resistant Factors of High TransmissibilityNature, 1967
- DNA replication and the division cycle in Escherichia coliJournal of Molecular Biology, 1967