Affiliation:
1. Department of Microbial Biotechnology, Centro Nacional de Biotecnología-CSIC, Campus UAM-Cantoblanco, Madrid, Spain
Abstract
ABSTRACT
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.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
68 articles.
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