AEM
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Galvão, T. C.
Right arrow Articles by de Lorenzo, V.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Galvão, T. C.
Right arrow Articles by de Lorenzo, V.
Agricola
Right arrow Articles by Galvão, T. C.
Right arrow Articles by de Lorenzo, V.
Applied and Environmental Microbiology, February 2005, p. 883-892, Vol. 71, No. 2
0099-2240/05/$08.00+0     doi:10.1128/AEM.71.2.883-892.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Adaptation of the Yeast URA3 Selection System to Gram-Negative Bacteria and Generation of a {Delta}betCDE Pseudomonas putida Strain

Teca Calcagno Galvão and Víctor de Lorenzo*

Department of Microbial Biotechnology, Centro Nacional de Biotecnología-CSIC, Campus UAM-Cantoblanco, Madrid, Spain

Received 3 August 2004/ Accepted 20 September 2004

A general procedure for efficient generation of gene knockouts in gram-negative bacteria by the adaptation of the Saccharomyces cerevisiae URA3 selection system is described. A Pseudomonas putida strain lacking the URA3 homolog pyrF (encoding orotidine-5'-phosphate decarboxylase) was constructed, allowing the use of a plasmid-borne copy of the gene as the target of selection. The delivery vector pTEC contains the pyrF gene and promoter, a conditional origin of replication (oriR6K), an origin of transfer (mobRK2), and an antibiotic selection marker flanked by multiple sites for cloning appropriate DNA segments. The versatility of pyrF as a selection system, allowing both positive and negative selection of the marker, and the robustness of the selection, where pyrF is associated with uracil prototrophy and fluoroorotic acid sensitivity, make this setup a powerful tool for efficient homologous gene replacement in gram-negative bacteria. The system has been instrumental for complete deletion of the P. putida choline-O-sulfate utilization operon betCDE, a mutant which could not be produced by any of the other genetic strategies available.


* Corresponding author. Mailing address: Centro Nacional de Biotecnología-CSIC, Campus de Cantoblanco, Madrid 28049, Spain. Phone: 34 915854536. Fax: 34 91 5854506. E-mail: vdlorenzo{at}cnb.uam.es.


Applied and Environmental Microbiology, February 2005, p. 883-892, Vol. 71, No. 2
0099-2240/05/$08.00+0     doi:10.1128/AEM.71.2.883-892.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. Microbiol. Mol. Biol. Rev. Eukaryot. Cell All ASM Journals

Copyright © 2005 by the American Society for Microbiology. All rights reserved.