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Agent-based modelling of iron cycling bacteria provides a framework for testing alternative environmental conditions and modes of action

Iron-reducing and iron-oxidizing bacteria are of interest in a variety of environmental and industrial applications. Such bacteria often co-occur at oxic-anoxic gradients in aquatic and terrestrial habitats. In this paper, we present the first computational agent-based model of microbial iron cyclin...

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Detalles Bibliográficos
Autores principales: Then, Andre, Ewald, Jan, Söllner, Natalie, Cooper, Rebecca E., Küsel, Kirsten, Ibrahim, Bashar, Schuster, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9115035/
https://www.ncbi.nlm.nih.gov/pubmed/35620008
http://dx.doi.org/10.1098/rsos.211553
Descripción
Sumario:Iron-reducing and iron-oxidizing bacteria are of interest in a variety of environmental and industrial applications. Such bacteria often co-occur at oxic-anoxic gradients in aquatic and terrestrial habitats. In this paper, we present the first computational agent-based model of microbial iron cycling, between the anaerobic ferric iron (Fe(3+))-reducing bacteria Shewanella spp. and the microaerophilic ferrous iron (Fe(2+))-oxidizing bacteria Sideroxydans spp. By including the key processes of reduction/oxidation, movement, adhesion, Fe(2+)-equilibration and nanoparticle formation, we derive a core model which enables hypothesis testing and prediction for different environmental conditions including temporal cycles of oxic and anoxic conditions. We compared (i) combinations of different Fe(3+)-reducing/Fe(2+)-oxidizing modes of action of the bacteria and (ii) system behaviour for different pH values. We predicted that the beneficial effect of a high number of iron-nanoparticles on the total Fe(3+) reduction rate of the system is not only due to the faster reduction of these iron-nanoparticles, but also to the nanoparticles’ additional capacity to bind Fe(2+) on their surfaces. Efficient iron-nanoparticle reduction is confined to pH around 6, being twice as high than at pH 7, whereas at pH 5 negligible reduction takes place. Furthermore, in accordance with experimental evidence our model showed that shorter oxic/anoxic periods exhibit a faster increase of total Fe(3+) reduction rate than longer periods.