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PMID: 11894964 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The origin of replication, oriC, and the dnaA protein are dispensable in stable DNA replication (sdrA) mutants of Escherichia coli K-12.

The EMBO journal ·Vol. 2 ·No. 3 ·1983-00-00 ·Pages 463-8

Kogoma T, von Meyenburg K

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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26 references, click to expand
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Article Info
Journal
The EMBO journal
Abbr.
EMBO J
ISSN
0261-4189
Published
1983-00-00
Pages
463-8
Language
English
Region
England
NLM ID
8208664
PMCID
PMC555155
Subset
IM
Grants
NIGMS NIH HHS · GM22092 · United States
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