
doi: 10.1007/bf00280310
pmid: 7513784
The nucleotide sequence was determined of the region upstream of the mukB gene of Escherichia coli. Two new genes were found, designated kicA and kicB (killing of cell); the gene order is kicB-kicA-mukB. Promoter activities were detected in the regions immediately upstream of kicB and kicA, but not in front of mukB. Gene disruption experiments revealed that the kicA disruptant was nonviable, but the kicB-disrupted mutant and the mutant lacking both the kicB and kicA genes were able to grow. When kicA disruptant cells bearing a temperature-sensitive replication plasmid carrying the kicA+ gene were grown at 30 degrees C and then transferred to 42 degrees C, the mutant cells gradually lost colony-forming ability, even in the presence of a mukB+ plasmid. Rates of protein synthesis, but not of RNA or DNA synthesis, fell dramatically during incubation at 42 degrees C. These results suggested that the kicB gene encodes a killing factor and the kicA gene codes for a protein that suppresses the killing function of the kicB gene product. It was also demonstrated that KicA and KicB can function as a post-segregational killing system, when the genes are transferred from the E. coli chromosome onto a plasmid.
DNA, Bacterial, Base Sequence, Escherichia coli Proteins, Molecular Sequence Data, Chromosome Mapping, Gene Expression Regulation, Bacterial, Repressor Proteins, Open Reading Frames, RNA, Bacterial, Bacterial Proteins, Genes, Bacterial, Escherichia coli, Mutagenesis, Site-Directed, Electrophoresis, Polyacrylamide Gel, Genes, Lethal, Amino Acid Sequence, Promoter Regions, Genetic, Cell Division, Gene Deletion, Plasmids
DNA, Bacterial, Base Sequence, Escherichia coli Proteins, Molecular Sequence Data, Chromosome Mapping, Gene Expression Regulation, Bacterial, Repressor Proteins, Open Reading Frames, RNA, Bacterial, Bacterial Proteins, Genes, Bacterial, Escherichia coli, Mutagenesis, Site-Directed, Electrophoresis, Polyacrylamide Gel, Genes, Lethal, Amino Acid Sequence, Promoter Regions, Genetic, Cell Division, Gene Deletion, Plasmids
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