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

被引:43
作者
Kita, K
Tsuda, J
Kato, T
Okamoto, K
Yanase, H
Tanaka, M
机构
[1] Tottori Univ, Dept Biotechnol, Tottori 6808552, Japan
[2] Gifu Int Inst Biotechnol, Gifu 5050116, Japan
关键词
D O I
10.1128/JB.181.21.6822-6827.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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-R;I) 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.
引用
收藏
页码:6822 / 6827
页数:6
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