Literature DB >> 31182498

The TonBm-PocAB System Is Required for Maintenance of Membrane Integrity and Polar Position of Flagella in Pseudomonas putida.

Kadi Ainsaar1, Hedvig Tamman1, Sergo Kasvandik2, Tanel Tenson2, Rita Hõrak3.   

Abstract

TonB-ExbB-ExbD-like energy transduction systems are widespread among Gram-negative bacteria. While most species have only one copy of tonB-exbBD genes, the Pseudomonas species possess more TonB-ExbBD homologues. One of them, the TonB3-PocA-PocB complex, was recently shown to be required for polar localization of FlhF and, thus, the flagella in Pseudomonas aeruginosa Here, we show that the orthologous TonBm-PocA-PocB complex is important for polar localization of FlhF and flagella in Pseudomonas putida as well. Additionally, the system is necessary for maintaining membrane integrity, as the inactivation of the TonBm-PocAB complex results in increased membrane permeability, lowered stress tolerance, and conditional cell lysis. Interestingly, the functionality of TonBm-PocAB complex is more important for stationary than for exponentially growing bacteria. The whole-cell proteome analysis provided a likely explanation for this growth phase dependence, as extensive reprogramming was disclosed in an exponentially growing tonBm deletion strain, while only a few proteomic changes, mostly downregulation of outer membrane proteins, were determined in the stationary-phase ΔtonBm strain. We propose that this response in exponential phase, involving, inter alia, activation of AlgU and ColR regulons, can compensate for TonBm-PocAB's deficiency, while stationary-phase cells are unable to alleviate the lack of TonBm-PocAB. Our results suggest that mislocalization of flagella does not cause the membrane integrity problems; rather, the impaired membrane intactness of the TonBm-PocAB-deficient strain could be the reason for the random placement of flagella.IMPORTANCE The ubiquitous Pseudomonas species are well adapted to survive in a wide variety of environments. Their success relies on their versatile metabolic, signaling, and transport ability but also on their high intrinsic tolerance to various stress factors. This is why the study of the stress-surviving mechanisms of Pseudomonas species is of utmost importance. The stress tolerance of Pseudomonads is mainly achieved through the high barrier property of their membranes. Here, we present evidence that the TonB-ExbBD-like TonBm-PocAB system is involved in maintaining the membrane homeostasis of Pseudomonas putida, and its deficiency leads to lowered stress tolerance and conditional cell lysis.
Copyright © 2019 American Society for Microbiology.

Entities:  

Keywords:  flagellum localization; growth phase dependence; membrane homeostasis; stress tolerance; swimming motility; whole-cell proteome

Mesh:

Substances:

Year:  2019        PMID: 31182498      PMCID: PMC6689306          DOI: 10.1128/JB.00303-19

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


  81 in total

1.  Quantification of known components of the Escherichia coli TonB energy transduction system: TonB, ExbB, ExbD and FepA.

Authors:  Penelope I Higgs; Ray A Larsen; Kathleen Postle
Journal:  Mol Microbiol       Date:  2002-04       Impact factor: 3.501

2.  The G-protein FlhF has a role in polar flagellar placement and general stress response induction in Pseudomonas putida.

Authors:  S Pandza; M Baetens; C H Park; T Au; M Keyhan; A Matin
Journal:  Mol Microbiol       Date:  2000-04       Impact factor: 3.501

3.  Involvement of the TonB system in tolerance to solvents and drugs in Pseudomonas putida DOT-T1E.

Authors:  P Godoy; M I Ramos-González; J L Ramos
Journal:  J Bacteriol       Date:  2001-09       Impact factor: 3.490

4.  Effects of combination of different -10 hexamers and downstream sequences on stationary-phase-specific sigma factor sigma(S)-dependent transcription in Pseudomonas putida.

Authors:  E L Ojangu; A Tover; R Teras; M Kivisaar
Journal:  J Bacteriol       Date:  2000-12       Impact factor: 3.490

5.  Genetic footprinting with mariner-based transposition in Pseudomonas aeruginosa.

Authors:  S M Wong; J J Mekalanos
Journal:  Proc Natl Acad Sci U S A       Date:  2000-08-29       Impact factor: 11.205

6.  Substrate specificities of MexAB-OprM, MexCD-OprJ, and MexXY-oprM efflux pumps in Pseudomonas aeruginosa.

Authors:  N Masuda; E Sakagawa; S Ohya; N Gotoh; H Tsujimoto; T Nishino
Journal:  Antimicrob Agents Chemother       Date:  2000-12       Impact factor: 5.191

7.  A panel of Tn7-based vectors for insertion of the gfp marker gene or for delivery of cloned DNA into Gram-negative bacteria at a neutral chromosomal site.

Authors:  B Koch; L E Jensen; O Nybroe
Journal:  J Microbiol Methods       Date:  2001-07       Impact factor: 2.363

8.  Interactions between the outer membrane ferric citrate transporter FecA and TonB: studies of the FecA TonB box.

Authors:  Monica Ogierman; Volkmar Braun
Journal:  J Bacteriol       Date:  2003-03       Impact factor: 3.490

Review 9.  Pedigree and taxonomic credentials of Pseudomonas putida strain KT2440.

Authors:  D Regenhardt; H Heuer; S Heim; D U Fernandez; C Strömpl; E R B Moore; K N Timmis
Journal:  Environ Microbiol       Date:  2002-12       Impact factor: 5.491

10.  Pseudomonas putida mutants in the exbBexbDtonB gene cluster are hypersensitive to environmental and chemical stressors.

Authors:  Patricia Godoy; María-Isabel Ramos-González; Juan L Ramos
Journal:  Environ Microbiol       Date:  2004-06       Impact factor: 5.491

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  2 in total

1.  Extracellular haem utilization by the opportunistic pathogen Pseudomonas aeruginosa and its role in virulence and pathogenesis.

Authors:  Susana Mouriño; Angela Wilks
Journal:  Adv Microb Physiol       Date:  2021-08-13       Impact factor: 3.517

2.  Decoupling Growth and Production by Removing the Origin of Replication from a Bacterial Chromosome.

Authors:  Marje Kasari; Villu Kasari; Mirjam Kärmas; Arvi Jõers
Journal:  ACS Synth Biol       Date:  2022-07-07       Impact factor: 5.249

  2 in total

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