Comparative analysis of the influence of BpfA and BpfG on biofilm development and current density in Shewanella oneidensis under oxic, fumarate- and anode-respiring conditions.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
05 Oct 2024
Historique:
received: 18 07 2024
accepted: 17 09 2024
medline: 6 10 2024
pubmed: 6 10 2024
entrez: 5 10 2024
Statut: epublish

Résumé

Biofilm formation by Shewanella oneidensis has been extensively studied under oxic conditions; however, relatively little is known about biofilm formation under anoxic conditions and how biofilm architecture and composition can positively influence current generation in bioelectrochemical systems. In this study, we utilized a recently developed microfluidic biofilm analysis setup with automated 3D imaging to investigate the effects of extracellular electron acceptors and synthetic modifications to the extracellular polymeric matrix on biofilm formation. Our results with the wild type strain demonstrate robust biofilm formation even under anoxic conditions when fumarate is used as the electron acceptor. However, this pattern shifts when a graphite electrode is employed as the electron acceptor, resulting in biofilm formation falling below the detection limit of the optical coherence tomography imaging system. To manipulate biofilm formation, we aimed to express BpfG with a single amino acid substitution in the catalytic center (C116S) and to overexpress bpfA. Our analyses indicate that, under oxic conditions, overarching mechanisms predominantly influence biofilm development, rather than the specific mutations we investigated. Under anoxic conditions, the bpfG mutation led to a quantitative increase in biofilm formation, but both strains exhibited significant qualitative changes in biofilm architecture compared to the controls. When an anode was used as the sole electron acceptor, both the bpfA and bpfG mutations positively impacted mean current density, yielding a 1.8-fold increase for each mutation.

Identifiants

pubmed: 39369013
doi: 10.1038/s41598-024-73474-w
pii: 10.1038/s41598-024-73474-w
doi:

Substances chimiques

Fumarates 0
Bacterial Proteins 0
Oxygen S88TT14065

Types de publication

Journal Article Comparative Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

23174

Informations de copyright

© 2024. The Author(s).

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Auteurs

Edina Marlen Klein (EM)

Institute of Technical Microbiology, University of Technology Hamburg, 21073, Hamburg, Germany.

Hannah Heintz (H)

Experimental Physics, Center for Biophysics, Saarland University, 66123, Saarbrücken, Germany.

René Wurst (R)

Institute of Technical Microbiology, University of Technology Hamburg, 21073, Hamburg, Germany.

Simon Schuldt (S)

Institute of Technical Microbiology, University of Technology Hamburg, 21073, Hamburg, Germany.

Hendrik Hähl (H)

Experimental Physics, Center for Biophysics, Saarland University, 66123, Saarbrücken, Germany.

Karin Jacobs (K)

Experimental Physics, Center for Biophysics, Saarland University, 66123, Saarbrücken, Germany.
Max Planck School Matter to Life, 69120, Heidelberg, Germany.

Johannes Gescher (J)

Institute of Technical Microbiology, University of Technology Hamburg, 21073, Hamburg, Germany. Johannes.gescher@tuhh.de.

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