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Applied and Environmental Microbiology, September 2002, p. 4658-4665, Vol. 68, No. 9
0099-2240/02/$04.00+0 DOI: 10.1128/AEM.68.9.4658-4665.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Leonardo C. A. Souza,2 Andrea C. D. Virgílio,1 Anelise G. Mariano,1 Renê R. Palma,1 and Patrícia B. Monteiro1*
Fundo de Defesa da Citricultura (Fundecitrus), Araraquara,1 Laboratório de Genética de Microorganismos, Departamento de Genética, ESALQ-USP, Piracicaba, São Paulo, Brazil2
Received 11 February 2002/ Accepted 17 June 2002
Mutagenesis by homologous recombination was evaluated in Xylella fastidiosa by using the bga gene, coding for ß-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 ß-galactosidase mutants. A promoterless chloramphenicol acetyltransferase gene was used to monitor the expression of the target gene and to select a cvaB mutant.
Present address: Laboratoire de Biologie Cellulaire et Moléculaire, IBVM, INRA 71, 33883 Villenave d'Ornon Cedex, France.
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