An international team of researchers, spearheaded by microbiologists Marc Mussmann and Alexander Loy from the University of Vienna, has unveiled a groundbreaking form of microbial metabolism that reshapes our understanding of elemental cycling in oxygen-starved environments. These newly identified microorganisms, dubbed MISO bacteria, perform a unique biochemical feat: they “breathe” iron minerals by oxidizing hydrogen sulfide, a toxic compound commonly found in marine sediments and wetlands. This discovery fundamentally alters existing paradigms, revealing that the interaction between sulfide and iron minerals is not merely a chemical phenomenon but also biologically catalyzed, with profound implications for ecosystem health and global element cycles.
The discovery hinges on the intricate biochemical mechanisms that allow these bacteria to couple the reduction of iron(III) oxide minerals with the oxidation of sulfide. Historically, the interaction between hydrogen sulfide and solid iron minerals was considered an abiotic reaction, producing intermediate compounds like elemental sulfur and iron monosulfide. However, MISO bacteria bypass these intermediate steps, directly converting sulfide into sulfate, a process that is both metabolically advantageous and environmentally significant. This bio-driven transformation not only detoxifies harmful hydrogen sulfide but simultaneously harnesses the released energy to fuel bacterial growth, in a manner reminiscent of how plants fix carbon dioxide through photosynthesis.
Elemental cycling of carbon, sulfur, nitrogen, and iron are foundational processes shaping Earth’s climate and ecosystem dynamics. These cycles are driven in large part by redox reactions—oxidation and reduction—that facilitate the movement and transformation of these elements across environmental compartments. Microorganisms serve as indispensable agents in these redox processes, employing diverse metabolic strategies to exploit available chemical energy in environments ranging from oxygen-rich surface waters to anoxic sediments. Among these, sulfur and iron cycles are intimately coupled, especially in oxygen-deprived settings, where redox reactions involving these elements dictate nutrient availability and influence the production or consumption of potent greenhouse gases such as methane and carbon dioxide.
Hydrogen sulfide, a hallmark of low-oxygen habitats, poses a toxic threat to most life forms due to its reactivity and potential to disrupt cellular processes. In sediments and wetlands where oxygen is scarce, specialized microbial communities generate this gas as a byproduct of organic matter decomposition. Traditionally, the fate of sulfide was attributed to purely chemical reactions with iron minerals, forming less harmful compounds that mitigate toxicity. However, the research led by Mussmann and Loy illustrates that this detoxification is substantially enhanced by microbial enzymatic activity. The MISO metabolism, by directly linking sulfide oxidation to iron reduction, accelerates the detoxification process beyond what chemistry alone can achieve.
Laboratory cultivation of MISO bacteria has provided concrete evidence supporting their pivotal role in natural sulfide oxidation. Controlled experiments demonstrated that the enzymatically mediated reaction rates significantly exceed those of the analogous abiotic reactions. This enzymatic efficiency suggests that microbial participation dominates sulfide transformation in natural settings, particularly in sediments rich in reactive iron. Genomic analyses further revealed that diverse bacterial and archaeal lineages harbor the genetic machinery necessary for MISO metabolism, indicating a widespread distribution across various ecosystems, including marine sediments, freshwater wetlands, and environments influenced by anthropogenic activity.
The global significance of this microbial metabolism cannot be overstated. Quantitative assessments estimate that MISO bacteria could be responsible for approximately 7% of the total sulfide oxidation to sulfate on a planetary scale. This estimate takes into account the vast inflows of reactive iron delivered by rivers and melting glaciers into the world’s oceans, which serve as crucial substrates for MISO-driven reactions. By mitigating sulfide toxicity and contributing to iron cycling, these microbes help stabilize aquatic environments against the expansion of hypoxic “dead zones”—areas where oxygen depletion severely hampers biodiversity and ecosystem services.
Crucially, the implications of this research extend beyond microbial ecology. By uncovering a biologically driven pathway that intertwines sulfur, iron, and carbon fluxes, this study reshapes our understanding of global biogeochemical processes. The metabolic versatility of MISO bacteria underscores the ecological ingenuity of microorganisms and their role as engineers of Earth’s chemical landscape. These findings also highlight potential feedback mechanisms in the context of climate change, where shifts in oxygen availability and iron fluxes could alter the distribution and activity of MISO populations, subsequently influencing greenhouse gas dynamics and aquatic ecosystem resilience.
From a broader perspective, elucidating MISO metabolism enriches the scientific narrative around anoxic microbial communities and their capacity for elemental regulation. The discovery paves the way for deeper exploration into microbial interactions with mineral substrates and the possibility of uncovering additional, yet unknown metabolic pathways that contribute to elemental cycling. It also opens avenues for biotechnological applications, where harnessing such microbes could inform strategies for bioremediation, especially in contexts where sulfide toxicity impairs environmental or industrial processes.
The meticulous work by the University of Vienna team illustrates the power of combining microbial cultivation, genomic insights, and geochemical analysis to unravel complex biogeochemical interdependencies. Their integrative approach has yielded a compelling case for revising current biogeochemical models that have, until now, largely neglected the biological component of sulfide and iron transformation in anoxic habitats. This paradigm shift could enhance predictive models of ecosystem function under changing environmental conditions.
Moreover, the environmental relevance of MISO bacteria extends to diverse natural and human-impacted settings. The enzymes and metabolic pathways they employ might serve as biomarkers to monitor ecosystem health or the progression of oxygen depletion in sediments. Understanding the spatial distribution and population dynamics of MISO communities could also inform conservation strategies aimed at preserving critical wetland and coastal habitats vulnerable to pollution and climate-induced hypoxia.
In summary, the revelation of microbial iron oxide respiration coupled to sulfide oxidation positions MISO bacteria as key players in Earth’s elemental cycles. Through a metabolic process that outpaces abiotic chemistry, these microbes detoxify harmful sulfide, contribute to iron cycling, and sustain carbon fixation in oxygen-deprived environments. Their global prevalence and efficiency underscore a hidden but influential microbial mechanism that shapes biogeochemical trajectories, aquatic ecosystem stability, and potentially climate feedback loops. The study heralds a new frontier in microbiology and environmental science, emphasizing the intricate ties between microbial life and planetary health.
Subject of Research: Microbial metabolism involving iron oxide respiration coupled to sulfide oxidation.
Article Title: Microbial iron oxide respiration coupled to sulfide oxidation.
News Publication Date: 27-Aug-2025
Web References:
- Research group of Alexander Loy
- Division of Microbial Ecology, University of Vienna
- Centre for Microbiology and Environmental Systems Science (CeMESS), University of Vienna
- FWF Cluster of Excellence – Microbiomes drive Planetary Health
References: DOI: 10.1038/s41586-025-09467-0
Image Credits: Alexander Loy
Keywords: MISO bacteria, microbial metabolism, iron oxide respiration, sulfide oxidation, biogeochemical cycles, sulfur cycle, iron cycle, microbial ecology, anoxic environments, groundwater microbiology, wetland microbiology, environmental microbiology, carbon fixation