Literature DB >> 10648517

A set of genes encoding a second toluene efflux system in Pseudomonas putida DOT-T1E is linked to the tod genes for toluene metabolism.

G Mosqueda1, J L Ramos.   

Abstract

Sequence analysis in Pseudomonas putida DOT-T1E revealed a second toluene efflux system for toluene metabolism encoded by the ttgDEF genes, which are adjacent to the tod genes. The ttgDEF genes were expressed in response to the presence of aromatic hydrocarbons such as toluene and styrene in the culture medium. To characterize the contribution of the TtgDEF system to toluene tolerance in P. putida, site-directed mutagenesis was used to knock out the gene in the wild-type DOT-T1E strain and in a mutant derivative, DOT-T1E-18. This mutant carried a Tn5 insertion in the ttgABC gene cluster, which encodes a toluene efflux pump that is synthesized constitutively. For site-directed mutagenesis, a cassette to knock out the ttgD gene and encoding resistance to tellurite was constructed in vitro and transferred to the corresponding host chromosome via the suicide plasmid pKNG101. Successful replacement of the wild-type sequences with the mutant cassette was confirmed by Southern hybridization. A single ttgD mutant, DOT-T1E-1, and a double mutant with knock outs in the ttgD and ttgA genes, DOT-T1E-82, were obtained and characterized for toluene tolerance. This was assayed by the sudden addition of toluene (0.3% [vol/vol]) to the liquid culture medium of cells growing on Luria-Bertani (LB) medium (noninduced) or on LB medium with toluene supplied via the gas phase (induced). Induced cells of the single ttgD mutant were more sensitive to sudden toluene shock than were the wild-type cells; however, noninduced wild-type and ttgD mutant cells were equally tolerant to toluene shock. Noninduced cells of the double DOT-T1E-82 mutant did not survive upon sudden toluene shock; however, they still remained viable upon sudden toluene shock if they had been previously induced. These results are discussed in the context of the use of multiple efflux pumps involved in solvent tolerance in P. putida DOT-T1E.

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Year:  2000        PMID: 10648517      PMCID: PMC94367          DOI: 10.1128/JB.182.4.937-943.2000

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  37 in total

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3.  A bacterial basic region leucine zipper histidine kinase regulating toluene degradation.

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Authors:  H Bolhuis; H W van Veen; B Poolman; A J Driessen; W N Konings
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5.  Role of the multidrug efflux systems of Pseudomonas aeruginosa in organic solvent tolerance.

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  36 in total

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Authors:  A Rojas; E Duque; G Mosqueda; G Golden; A Hurtado; J L Ramos; A Segura
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4.  In vivo and in vitro evidence that TtgV is the specific regulator of the TtgGHI multidrug and solvent efflux pump of Pseudomonas putida.

Authors:  Antonia Rojas; Ana Segura; María Eugenia Guazzaroni; Wilson Terán; Ana Hurtado; María Trinidad Gallegos; Juan L Ramos
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5.  TtgV bound to a complex operator site represses transcription of the promoter for the multidrug and solvent extrusion TtgGHI pump.

Authors:  María-Eugenia Guazzaroni; Wilson Terán; Xiaodong Zhang; María-Trinidad Gallegos; Juan L Ramos
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7.  TtgV represses two different promoters by recognizing different sequences.

Authors:  Sandy Fillet; Marisela Vélez; Duo Lu; Xiaodong Zhang; María-Trinidad Gallegos; Juan L Ramos
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Authors:  Edward W Yu; Julio R Aires; Hiroshi Nikaido
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9.  Proteomic analysis reveals the participation of energy- and stress-related proteins in the response of Pseudomonas putida DOT-T1E to toluene.

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10.  The RpoT regulon of Pseudomonas putida DOT-T1E and its role in stress endurance against solvents.

Authors:  Estrella Duque; José-Juan Rodríguez-Herva; Jesús de la Torre; Patricia Domínguez-Cuevas; Jesús Muñoz-Rojas; Juan-Luis Ramos
Journal:  J Bacteriol       Date:  2006-10-27       Impact factor: 3.490

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