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Appl Environ Microbiol ; 68(9): 4658-65, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12200328

ABSTRACT

Mutagenesis by homologous recombination was evaluated in Xylella fastidiosa by using the bga gene, coding for beta-galactosidase, as a model. Integration of replicative plasmids by homologous recombination between the cloned truncated copy of bga and the endogenous gene was produced by one or two crossover events leading to beta-galactosidase mutants. A promoterless chloramphenicol acetyltransferase gene was used to monitor the expression of the target gene and to select a cvaB mutant.


Subject(s)
Gammaproteobacteria/genetics , beta-Galactosidase/genetics , Alleles , Chloramphenicol/pharmacology , Chloramphenicol O-Acetyltransferase/biosynthesis , Genes, Reporter , Mutagenesis, Insertional , Plasmids/genetics , Recombination, Genetic , Replication Origin/genetics , beta-Galactosidase/deficiency , beta-Galactosidase/metabolism
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