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Identification of E. coli K12 chromosomal insertion sites of bacteriophage φ297

机译:鉴定噬菌体φ297的大肠杆菌K12染色体插入位点

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摘要

Objective:To identify the specific integration site of prophage φ297 in the host of E. coli K12 chromosome. Methods:Using molecular techniques such as Siebert PCR for walking from the int gene of prophage 297, which is similar to that of phage 933W to an unknown region in genomic DNA. A special adaptor is ligated to the ends of DNA fragments generated by digestion of genomic DNA with restriction enzymes that generates blunt ended fragments. Clone and subclone of PCR products, DNA sequencing and data analysis were used in this study. Results:The attL, attR and the core sequences were determined. The bacterial attachment site of phage φ297 was located in the yecE gene of E. coli K12. Conclusion:The phage φ297 integrates into the yecE gene of the E. coli K12 genome.
机译:目的:确定大肠杆菌K12染色体宿主中噬菌体φ297的特异性整合位点。方法:使用分子生物学技术,例如Siebert PCR,从噬菌体297的int基因(与噬菌体933W相似)步行到基因组DNA的未知区域。将特殊的衔接子连接到用限制酶消化基因组DNA产生的DNA片段的末端,所述限制酶产生平末端的片段。本研究使用了PCR产品的克隆和亚克隆,DNA测序和数据分析。结果:确定了attL,attR和核心序列。噬菌体φ297的细菌附着位点位于大肠杆菌K12的yecE基因中。结论:噬菌体φ297已整合到大肠杆菌K12基因组的yecE基因中。

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