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使用噬菌体P1作为Tn5插入诱变的载体。

Use of bacteriophage P1 as a vector for Tn5 insertion mutagenesis.

作者信息

Quinto M, Bender R A

出版信息

Appl Environ Microbiol. 1984 Feb;47(2):436-8. doi: 10.1128/aem.47.2.436-438.1984.

DOI:10.1128/aem.47.2.436-438.1984
PMID:6324677
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC239691/
Abstract

Infection of a strain lysogenic for bacteriophage P1 CM with P1::Tn5 followed by simultaneous selection for the chloroamphenicol resistance associated with the resident prophage and the kanamycin resistance associated with Tn5 results in a large number of independent Tn5 insertion mutations. This superinfection-selection protocol is a fast, easy, and safe way to isolate null mutations in enteric bacteria without generating unwanted cryptic mutations elsewhere in the genome.

摘要

用P1::Tn5感染对噬菌体P1 CM呈溶原性的菌株,随后同时选择与驻留原噬菌体相关的氯霉素抗性和与Tn5相关的卡那霉素抗性,会产生大量独立的Tn5插入突变。这种超感染选择方案是一种快速、简便且安全的方法,可用于在肠道细菌中分离无效突变,而不会在基因组的其他位置产生不需要的隐蔽突变。

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本文引用的文献

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