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Mechanisms of resistance to chloramphenicol in Pseudomonas putida KT2440.


ABSTRACT: Pseudomonas putida KT2440 is a chloramphenicol-resistant bacterium that is able to grow in the presence of this antibiotic at a concentration of up to 25 ?g/ml. Transcriptomic analyses revealed that the expression profile of 102 genes changed in response to this concentration of chloramphenicol in the culture medium. The genes that showed altered expression include those involved in general metabolism, cellular stress response, gene regulation, efflux pump transporters, and protein biosynthesis. Analysis of a genome-wide collection of mutants showed that survival of a knockout mutant in the TtgABC resistance-nodulation-division (RND) efflux pump and mutants in the biosynthesis of pyrroloquinoline (PQQ) were compromised in the presence of chloramphenicol. The analysis also revealed that an ABC extrusion system (PP2669/PP2668/PP2667) and the AgmR regulator (PP2665) were needed for full resistance toward chloramphenicol. Transcriptional arrays revealed that AgmR controls the expression of the pqq genes and the operon encoding the ABC extrusion pump from the promoter upstream of open reading frame (ORF) PP2669.

SUBMITTER: Fernandez M 

PROVIDER: S-EPMC3264264 | biostudies-literature | 2012 Feb

REPOSITORIES: biostudies-literature

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Mechanisms of resistance to chloramphenicol in Pseudomonas putida KT2440.

Fernández Matilde M   Conde Susana S   de la Torre Jesús J   Molina-Santiago Carlos C   Ramos Juan-Luis JL   Duque Estrella E  

Antimicrobial agents and chemotherapy 20111205 2


Pseudomonas putida KT2440 is a chloramphenicol-resistant bacterium that is able to grow in the presence of this antibiotic at a concentration of up to 25 μg/ml. Transcriptomic analyses revealed that the expression profile of 102 genes changed in response to this concentration of chloramphenicol in the culture medium. The genes that showed altered expression include those involved in general metabolism, cellular stress response, gene regulation, efflux pump transporters, and protein biosynthesis.  ...[more]

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