Plasmids for ectopic integration in Bacillus subtilis

Plasmids have been constructed that allow integration by a double recombination event at the thrC locus of the Bacillus subtilis (Bs) chromosome. These plasmids can be used either for construction of merodiploid strains and complementation analysis, or for construction of transcriptional fusions to...

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Veröffentlicht in:Gene 1996-11, Vol.180 (1), p.57-61
Hauptverfasser: Guérout-Fleury, Anne-Marie, Frandsen, Niels, Stragier, Patrick
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creator Guérout-Fleury, Anne-Marie
Frandsen, Niels
Stragier, Patrick
description Plasmids have been constructed that allow integration by a double recombination event at the thrC locus of the Bacillus subtilis (Bs) chromosome. These plasmids can be used either for construction of merodiploid strains and complementation analysis, or for construction of transcriptional fusions to the Escherichia coli lacZ gene. The plasmids contain an antibiotic (An) marker selectable in Bs, as well as an additional An marker outside of the region that can recombine into the chromosome. When used in conjunction with recipient strains containing a third An marker at their thrC locus, these plasmids allow easy identification of transformants issued from a marker exchange event without additional Campbell-type integration. The existing plasmids used for ectopic integration at the amyE locus have been modified similarly.
doi_str_mv 10.1016/S0378-1119(96)00404-0
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects alpha-Amylases - genetics
amyE locus
Bacillus subtilis
Bacillus subtilis - genetics
Carbon-Oxygen Lyases
Double recombination event
Drug Resistance, Microbial - genetics
Genetic Vectors
lacZ fusion
Lyases - genetics
Merodiploid
Molecular Sequence Data
Plasmids
Recombination, Genetic
thrC locus
Transduction, Genetic
Transformation, Genetic
title Plasmids for ectopic integration in Bacillus subtilis
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