Editorial: Microbial Electron Transport
Lucian C Staicu, Catarina M Paquete

Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
- —MOSTMICRO-ITQB
- —LS4FUTURE Associated Laboratory
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Taxonomy
TopicsMicrobial Fuel Cells and Bioremediation
Electron transport is fundamental for all living organisms to generate the cellular energy needed to sustain growth. Microorganisms display an exceptional versatility in their use of electron donors and acceptors, including metals and metalloids, making them key players in Earth’s biogeochemical cycles (Staicu and Barton 2024). In recent decades, microbes capable of extracellular electron transfer have captured growing scientific and industrial interest. Their unique ability to exchange electrons beyond the cell membrane opens exciting opportunities in bioremediation, microbial electrochemical technologies, and the sustainable production of biofuels and chemicals. The thematic issue of FEMS Microbiology Ecology, entitled “Microbial Electron Transport”, brings together one review and seven research articles that collectively advance our understanding of microbial respiration and electron transport across environmental and applied contexts.
Environmental variability often determines the growth and activity of microorganisms. Bottaro et al. (2025) investigate how salinity and pH influence microbial communities capable of coupling nitrate reduction with Fe(II) oxidation. Using microcosm and enrichment experiments, they demonstrate that microbes can adapt to pH and salt fluctuations, with pH emerging as a key control factor. Their findings reveal that Fe(III) mineral precipitation is favored at neutral pH, shedding light on the intricate balance between environmental chemistry and microbial metabolism. In a different study, Soares et al. (2025) examine microbial community structure dynamics with Fe- and S-rich lithology in a pyritic coal-based aquifer. Their study shows that Fe(II)-oxidizing bacteria from the Gallionella and Sideroxydans genera dominate anthracitic and low volatile coal ranks, whereas S-oxidizing bacteria, such as Sulfuricurvum and Sulfurovum genera, prevail in medium volatile coal ranks. These results underscore the importance of hydrogeological and geochemical conditions in shaping microbial communities and regional Fe- and S-biogeochemistry. Cultivating chemolithotrophic neutrophilic Fe-oxidizing bacteria remains notoriously difficult due to the challenge of replicating their native environments in the laboratory. Addressing this limitation, Uchijima et al. (2025) introduce a custom-designed growth medium that simulates the energy substrates and nutrients typical of natural Fe-rich habitats. This innovation successfully enriches members of the Gallionellaceae family, opening new avenues for studying their metabolism and respiratory processes.
The interplay between Fe(II) oxidation and Fe(III) reduction is a defining feature of many aquatic systems. Nikeleit et al. (2025) explore these dynamics in a dimictic lake, revealing that potential Fe-metabolizing bacteria, including Chlorobium, Thiodictyon, Sideroxydans, Geobacter, and Rhodoferrax thrive predominantly under anoxic conditions. Their work highlights how organic substrates and redox gradients control the balance of iron cycling in natural waters.
The metabolic potential of Thiobacillus denitrificans as a nitrate-reducing Fe(II) oxidizer remains an open question. Toward this, Becker et al. (2025) approach this puzzle through multiple transfer cultivation experiments, using Fe(II) and nitrate as the sole electron donor and acceptor, respectively. Their findings suggest that T. denitrificans can perform the first step of denitrification using Fe(II) as an electron donor, yet it fails to sustain growth under these conditions.
A deeper understanding of microbial electron transport and its link to mineral transformations is vital for advancing biotechnological processes. Staicu et al. (2025) review how microbial interactions with biominerals, such as FeS_x_, S^0^, AsS, and Se^0^ influence both basic biological functions and applied processes. Their analysis bridges fundamental and applied perspectives, discussing implications for bioelectrochemical systems and highlighting the promise of this multidisciplinary field.
Microbial electron exchange is not limited to single species, as it also drives syntrophic cooperation. Feliu-Paradeda et al. (2025) demonstrate that co-cultures of two Clostridium species grown in the presence of conductive materials exhibited enhanced microbial interactions, boosting the production of elongated short-chain fatty acids and alcohols. These findings underscore the potential of conductive materials to mediate electron transfer between microbes, implying biochemical yields. In another contribution, Boltz and Rittmann (2025) explore autotrophic and heterotrophic bacteria in microbial communities based on H_2_-autotrophy. Through simulations under varying solids retention times, they revealed that autotrophic hydrogenotrophs dominate the active biomass, while non-active solids accumulate over time, providing insights into the stability and efficiency of mixed microbial systems.
Collectively, the studies presented in this thematic issue highlight that microbial electron transport is not only a cornerstone of metabolism but also a driver for ecological and technological innovation. We have high hopes that the corpus of work reported in this thematic issue will inspire further research on the multifaceted aspects of microbial electron transfer, from iron cycling in natural waters to engineering co-cultures for sustainable production, ultimately advancing our ability to harness these processes to meet pressing societal and environmental challenges.
The reference list from the paper itself. Each links out to its DOI / PubMed record.
- 1Becker S, Dang TT, Wei R et al. Evaluation of Thiobacillus denitrificans’ sustainability in nitrate-reducing Fe(II) oxidation and the potential significance of Fe (II) as a growth-supporting reductant. FEMS Microbiol Ecol. 2025;101:fiaf 024. 10.1093/femsec/fiaf 024.40097297 PMC 11963766 · doi ↗ · pubmed ↗
- 2Boltz JP, Rittmann BE. Microbial ecology of nitrate-, selenate-, selenite-, and sulfate-reducing bacteria in a H 2-driven bioprocess. FEMS Microbiol Ecol. 2024;100:fiae 125. 10.1093/femsec/fiae 125.39277779 PMC 11523051 · doi ↗ · pubmed ↗
- 3Bottaro M, Abramov S, Amils R et al. Impact of p H and salinity fluctuations on oxidation of Fe(II) by nitrate-reducing microorganisms enriched from the reduced tidal sediment of an extreme acidic river (Río Tinto, Spain). FEMS Microbiol Ecol. 2025;101:fiaf 083. 10.1093/femsec/fiaf 083.40880130 PMC 12475565 · doi ↗ · pubmed ↗
- 4Feliu-Paradeda L, Puig S, Bañeras L. Electron conductive compounds alter fermentative pathways and cooperation in Clostridium carboxidivorans and Clostridium acetobutylicum in co-culture. FEMS Microbiol Ecol. 2025;101:fiaf 090. 10.1093/femsec/fiaf 090.40972045 PMC 12451442 · doi ↗ · pubmed ↗
- 5Nikeleit V, Maisch M, Straub D et al. Cryptic iron cycling influenced by organic carbon availability in a seasonally stratified lake. FEMS Microbiol Ecol. 2025;101:fiaf 029. 10.1093/femsec/fiaf 029.40113245 PMC 11974394 · doi ↗ · pubmed ↗
- 6Soares A, Edwards Rassner SA, Edwards A et al. Hydrogeological and geological partitioning of iron and sulfur cycling bacterial consortia in subsurface coal-based mine waters. FEMS Microbiol Ecol. 2025;101:fiaf 039. 10.1093/femsec/fiaf 039.40205489 PMC 12001885 · doi ↗ · pubmed ↗
- 7Staicu LC, Barton LL. Geomicrobiology: Natural and Anthropogenic Settings. Cham: Springer, 2024. 10.1007/978-3-031-54306-7 · doi ↗
- 8Staicu LC, Cosmidis J, Mansor M et al. Microbial respiration—a biomineral perspective. FEMS Microbiol Ecol. 2025;101:fiaf 093. 10.1093/femsec/fiaf 093.40996469 PMC 12481199 · doi ↗ · pubmed ↗
