Abstract
The sdrA224 mutants of Escherichia coli K-12, capable of continued DNA replication in the absence of protein synthesis (stable DNA replication), tolerate inactivation of the dnaA gene by insertion of transposon Tn10. Furthermore, oriC, the origin of E. coli chromosome replication, can be deleted from the chromosome of sdrA mutants without loss of viability. The results suggest the presence of a second, normally repressed, initiation system for chromosome replication alternative to the 'normal' dnaA+ oriC+-dependent initiation mechanism.
MeSH Terms
Bacterial Proteins/genetics
DNA Replication
DNA, Bacterial/biosynthesis
DNA-Binding Proteins/genetics
Escherichia coli/genetics
Genes, Viral
Mutagenesis
Replication Origin
Transposases
Chemicals
Bacterial Proteins
DNA, Bacterial
DNA-Binding Proteins
DnaA protein, Bacteria
Transposases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kogoma T
Department of Microbiology, The Technical University of Denmark, Lyngby-Copenhagen.
von Meyenburg K
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