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从假单胞菌中鉴定一个隐秘质粒,并利用其温度敏感衍生物进行遗传操作。

Characterization of a cryptic plasmid from Pseudomonas sp. and utilization of its temperature-sensitive derivatives for genetic manipulation.

机构信息

Molecular Microbiology Laboratory, Faculty of Life Sciences, Northwest University, 229 Taibai Road North, Xi'an, Shaanxi 710069, PR China.

出版信息

Plasmid. 2010 Sep;64(2):110-7. doi: 10.1016/j.plasmid.2010.05.003. Epub 2010 May 24.

Abstract

A new cryptic plasmid, named pMM101, in an environmental Pseudomonas sp. has been isolated, and its 2140-bp DNA sequence has been determined and analyzed. One open reading frame (Rep(MM)) similar to the rep gene of the rolling-circle replicon (RCR) group VIII has been allocated in the replication region where a putative double-strand origin dso and single-strand origin sso could also be identified. After in vitro mutagenesis by error-prone PCR and introduced into Pseudomonas aeruginosa PAO1, a mutant plasmid which was stably maintained at 30 degrees C but not at 42 degrees C was isolated and analyzed. It had two nucleotide substitutions in the putative sso and dso regions. Replacing one of the two sites with wild type sequence resulted in similar instability at 42 degrees C, indicating either mutation could result in the temperature-sensitive trait. Using the mutant replicon, a Pseudomonas (temperature-sensitive)-Escherichia coli shuttle vector, pUM109, has been constructed and used successfully to disrupt P. aeruginosa genes. This temperature-sensitive vector provides an alternative tool for genetic manipulations in this industrially as well as medically important bacterium.

摘要

已分离到一株环境假单胞菌中的新型隐秘质质粒 pMM101,并测定和分析了其 2140bp 的 DNA 序列。复制区中分配有一个与 RCR 组 VIII 的 rep 基因相似的开放阅读框(Rep(MM)),该区域还可以识别出一个假定的双链起始点 dso 和单链起始点 sso。经易错 PCR 体外诱变并引入铜绿假单胞菌 PAO1 后,分离和分析了一种能够在 30°C 下稳定保持而在 42°C 下不能稳定保持的突变质粒。该突变质粒在假定的 sso 和 dso 区域有两个核苷酸取代。用野生型序列替换两个位点中的一个,在 42°C 时也会导致类似的不稳定性,表明这两种突变都可能导致温度敏感性。利用该突变复制子,构建了一种假单胞菌(温度敏感)-大肠杆菌穿梭载体 pUM109,并成功用于破坏铜绿假单胞菌的基因。这种温度敏感载体为该在工业和医学上均具有重要意义的细菌的遗传操作提供了另一种工具。

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