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PMID: 10542186 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Evidence of horizontal transfer of the EcoO109I restriction-modification gene to Escherichia coli chromosomal DNA.

Journal of bacteriology ·Vol. 181 ·No. 21 ·1999-11-00 ·Pages 6822-7

Kita K, Tsuda J, Kato T, Okamoto K, Yanase H, Tanaka M

Abstract

A DNA fragment carrying the genes coding for EcoO109I endonuclease and EcoO109I methylase, which recognize the nucleotide sequence 5'-(A/G)GGNCC(C/T)-3', was cloned from the chromosomal DNA of Escherichia coli H709c. The EcoO109I restriction-modification (R-M) system was found to be inserted between the int and psu genes from satellite bacteriophage P4, which were lysogenized in the chromosome at the P4 phage attachment site of the corresponding leuX gene observed in E. coli K-12 chromosomal DNA. The sid gene of the prophage was inactivated by insertion of one copy of IS21. These findings may shed light on the horizontal transfer and stable maintenance of the R-M system.

MeSH Terms
Amino Acid Sequence Base Sequence Chromosome Mapping Chromosomes, Bacterial Cloning, Molecular DNA Restriction-Modification Enzymes/chemistry,genetics Deoxyribonucleases, Type II Site-Specific/chemistry,genetics Escherichia coli/enzymology,genetics Genes, Bacterial Molecular Sequence Data Sequence Analysis, DNA
Chemicals
DNA Restriction-Modification Enzymes Deoxyribonucleases, Type II Site-Specific RGGNCCY-specific type II deoxyribonucleases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Kita K
Department of Biotechnology, Tottori University, 4-101 Koyama, Tottori 680-8552, Gifu 505-0116, Japan. kita@bio.tottori-u.ac.jp
Tsuda J
Kato T
Okamoto K
Yanase H
Tanaka M
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1999-11-00
Pages
6822-7
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC94149
Subset
IM
Databases
GENBANK
AF157599
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