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Electrotransformation and natural transformation of Streptococcus pneumoniae:requirement of DNA processing for recombination

Laboratoire de Microbiologie et de GCnCtique MolCculaire du CNRS and UniversitC Paul Sabatier, 118 route de Narbonnei 31062 Toulouse Cedex, France 2 Author for correspondence: Jacques Lefrangois. Tel: +33 5 61 33 59 71. Fax: +33 5 61 33 58 86.e-mail: jacques@ibcg.biotoul.fr ABSTRACT SUMMARY: Electro...

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Bibliographic Details
Published in:Microbiology (Society for General Microbiology) 1998-11, Vol.144 (11), p.3061-3068
Main Authors: LefranGois, Jacques, Samrakandi, M. Mustapha, Sicard, A. Michel
Format: Article
Language:English
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Summary:Laboratoire de Microbiologie et de GCnCtique MolCculaire du CNRS and UniversitC Paul Sabatier, 118 route de Narbonnei 31062 Toulouse Cedex, France 2 Author for correspondence: Jacques Lefrangois. Tel: +33 5 61 33 59 71. Fax: +33 5 61 33 58 86.e-mail: jacques@ibcg.biotoul.fr ABSTRACT SUMMARY: Electrotransformation has been used as a tool to introduce genes carried on replicative vectors in hundreds of bacterial species. In this study, the technique was used to try to obtain recombination of markers in the chromosome of the natura IIy transformable bacterium Streptococcus pneumoniae. Recombination was not observed even using naturally competent cultures. Both chromosomal and cloned DNA, denatured or native, were without effect. These results suggest that it is not sufficient to introduce DNA into the cell to obtain recombinants in this bacterium. The integration of markers into the chromosome in naturally competent cells must require DNA processing during entry. Electrotransformation of replicating plasmids is red-independent but can be facilitated by a red-dependent process. This facilitation required the induction of the natural competence machinery, probably involving partial homologous pairing. Keywords: electrotransformation, recombination, plasmid facilitation
ISSN:1350-0872
1465-2080
DOI:10.1099/00221287-144-11-3061