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Note: Evidence of Horizontal Transfer of the EcoO109I Restriction-Modification Gene to Escherichia coli Chromosomal DNA

机译:注:EcoO109I限制性修饰基因向大肠杆菌染色体DNA水平转移的证据

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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-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.
机译:从大肠杆菌H709c的染色体DNA中克隆了带有识别EcoO109I内切酶和EcoO109I甲基化酶的基因的DNA片段,该基因识别核苷酸序列5'-(A / G)GGNCC(C / T)-3'。已发现EcoO109I限制性修饰(RM)系统插入了来自卫星噬菌体P4的int和psu基因之间,它们在染色体中在大肠杆菌K-12中观察到的相应leuX基因的P4噬菌体附着位点处被裂解。染色体DNA。通过插入一份IS21,灭活了该噬菌体的sid基因。这些发现可能为R-M系统的水平转移和稳定维护提供了启示。

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