Neither absence nor excess of λ O initiator‐digesting ClpXP protease affects λ plasmid or phage replication in Escherichia coli
- 1 August 1994
- journal article
- Published by Wiley in Molecular Microbiology
- Vol. 13 (3) , 469-474
- https://doi.org/10.1111/j.1365-2958.1994.tb00441.x
Abstract
Owing to rapid proteolysis of the coliphage λ-coded initiator protein, λ O, this protein is considered to carry a rate–limiting step in λ DNA replication. The discovery of ClpXP protease responsible for λ O protein turnover allowed an opportunity to verify this hypothesis. However, neither absence nor excess of this protease significantly affected the transformation efficiency and copy number of λ plasmid, or the Kinetics of the λ phage growth. These results are also incompatible with the hypothesis that the stabilization of λ O plays a role in the switch from early (circle-to-circle) to late (rolling-circle) λ phage DNA replication. Tran-scriptional activation of oriλ probably assisted by the Escherichia coli DnaA function, remains as the possible rate-limiting step in λ DNA replication.Keywords
This publication has 24 references indexed in Scilit:
- High copy number of the pUC plasmid results from a Rom/Rop‐suppressible point mutation in RNA IIMolecular Microbiology, 1992
- Inheritance of the replication complex by one of two daughter copies during λ plasmid replication in Escherichia coliJournal of Molecular Biology, 1992
- Stability of coliphage λ DNA replication initiator, the λO proteinJournal of Molecular Biology, 1992
- Control of plasmid replication—How do DNA iterons set the replication frequency?Cell, 1990
- Regulation of βdv plasmid DNA replicationJournal of Molecular Biology, 1986
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985
- A mathematical model for λdv plasmid replication: Analysis of wild-type plasmidPlasmid, 1984
- Protein degradation in E. coli: The ion mutation and bacteriophage lambda N and cll protein stabilityCell, 1981
- Cloning of the replication gene O of E. coli bacteriophage lambda and its expression under the control of the lac promoterGene, 1980
- Synthesis and decay of λ DNA replication proteins in minicellsBiochemical and Biophysical Research Communications, 1980