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• W2103131002 startingPage "2520" @default.
• W2103131002 abstract "A simple, effective method of unlabeled, stable gene insertion into bacterial chromosomes has been developed. This utilizes an insertion cassette consisting of an antibiotic resistance gene flanked by dif sites and regions homologous to the chromosomal target locus. dif is the recognition sequence for the native Xer site-specific recombinases responsible for chromosome and plasmid dimer resolution: XerC/XerD in Escherichia coli and RipX/CodV in Bacillus subtilis. Following integration of the insertion cassette into the chromosomal target locus by homologous recombination, these recombinases act to resolve the two directly repeated dif sites to a single site, thus excising the antibiotic resistance gene. Previous approaches have required the inclusion of exogenous site-specific recombinases or transposases in trans; our strategy demonstrates that this is unnecessary, since an effective recombination system is already present in bacteria. The high recombination frequency makes the inclusion of a counter-selectable marker gene unnecessary." @default.
• W2103131002 created "2016-06-24" @default.
• W2103131002 creator A5038343335 @default.
• W2103131002 creator A5086918152 @default.
• W2103131002 date "2006-04-01" @default.
• W2103131002 modified "2023-09-27" @default.
• W2103131002 title "An Efficient Method of Selectable Marker Gene Excision by Xer Recombination for Gene Replacement in Bacterial Chromosomes" @default.
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• W2103131002 doi "https://doi.org/10.1128/aem.72.4.2520-2525.2006" @default.
• W2103131002 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1449051" @default.
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