| Literature DB >> 12480112 |
Peter G Agron1, Patricia Sobecky, Gary L Andersen.
Abstract
We present a simple approach that permits any circular plasmid, such as uncharacterized plasmids from diverse prokaryotes, to be established in Escherichia coli, thereby facilitating subsequent structural and functional studies. An in vitro transposition reaction is used to introduce a well-characterized replicon and selectable marker into purified plasmids, which are then used to transform E. coli. The approach was demonstrated using a small 3.4-kb archaeal plasmid and a large 60-kb uncharacterized plasmid from a Gram-negative bacterium. Replicon function in E. coli was tested for each plasmid, and direct sequencing of the large plasmid revealed similarity to restriction-modification systems. Copyright 2002 Federation of European Microbiological SocietiesEntities:
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Year: 2002 PMID: 12480112 DOI: 10.1111/j.1574-6968.2002.tb11483.x
Source DB: PubMed Journal: FEMS Microbiol Lett ISSN: 0378-1097 Impact factor: 2.742