Evidence map›Paper›PMID 40754734›Full record

ArticleMicrobial biotechnology2025

The TonB-Dependent Transport System Facilitates the Uptake of Inorganic Metal Mediators in Pseudomonas putida KT2440 in a Bioelectrochemical System.

Anna Weimer, Jens Krömer, Bin Lai, Christoph Wittmann

Abstract read
In one paragraph

Article in Microbial biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Anna WeimerInstitute of Systems Biotechnology, Saarland University, Saarbrücken, Germany.
Jens KrömerSystems Biotechnology Group, Helmholtz Centre for Environmental Research-UFZ, Leipzig, Germany.
Bin LaiBMBF Junior Research Group Biophotovoltaics, Helmholtz Centre for Environmental Research-UFZ, Leipzig, Germany.ORCID https://orcid.org/0000-0002-1583-0221
Christoph WittmannInstitute of Systems Biotechnology, Saarland University, Saarbrücken, Germany.ORCID https://orcid.org/0000-0002-7952-985X

Funding

Deutsche Forschungsgemeinschaft KR 4935/1-1Deutsche Forschungsgemeinschaft WI 1796/4-1Projekt DEAL
6 · The paper itself

Abstract

Mediator-based extracellular electron transfer (EET) in a bioelectrochemical system is a unique approach to regulate the microbial redox and energy metabolism of Pseudomonas putida KT2440, which enables a new-to-nature high product yield under anaerobic conditions. Previous studies identified respiratory complex III in the inner membrane as a key redox protein involved in mediator (ferricyanide) interactions, but the exact mechanism through which the mediator crosses the outer membrane to extract electrons from membrane-bound redox proteins and transfer them to the anode remains unclear. In this study, we demonstrated the critical role of the TonB-dependent system, a widespread transportation system in gram-negative bacteria, in the mediator-based EET process. Transcriptomic analyses revealed significant upregulation of TonB-dependent receptors in response to ferricyanide exposure, suggesting their involvement in mediator uptake. Deletion of the TonB complex resulted in a > 50% decrease in the mediator reduction rate and current output, confirming the role of the TonB-dependent system in mediator transport. Additionally, increasing passive diffusion through the overexpression of the general porin OprF increased cell permeability and the mediator reduction rate, but it failed to compensate for the absence of TonB-dependent transport. These findings suggest that both systems act in a complementary manner: the TonB-dependent system is likely the primary mechanism for periplasmic mediator uptake, whereas OprF is likely involved mainly in mediator efflux. Further bioelectrochemical system experiments demonstrated that, with a functional TonB-dependent system, OprF overexpression increased current output, glucose consumption, and 2-ketogluconate production, suggesting a viable strategy for enhancing the efficacy of mediator-based EET. This work reveals the major mediator transport mechanism in P. putida and deepens the understanding of the mediator-based EET pathway, laying the basis for future rational engineering of EET kinetics and facilitating the integration of mediator-based electron transfer into industrial biotechnology to push its process boundaries.

Indexed as

Bacterial ProteinsBioelectric Energy SourcesMembrane ProteinsMetalsPseudomonas putidaBiological TransportElectron TransportGene Expression ProfilingGene Expression Regulation, BacterialOxidation-ReductionBacterial ProteinsMembrane ProteinsMetalstonB protein, Bacteria2‐ketogluconatebioelectrochemical systemextracellular electron transferferricyanidemediator transportPseudomonas putida KT2440redox mediatorTonB

Identifiers

PMID40754734
PMCPMC12319065

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.