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Santha, K.

Publications and source records attributed to Santha, K..

2 recordsLinked to original sources

A sulfur-cycling co-culture alters iron sulfide diagenesis and pyritization

Iron sulfide minerals play a key role in modulating the oxygenation of Earth s atmosphere and represent an archive for reconstructing past environmental conditions. In anoxic sedimentary environments, microbially produced sulfide reacts with iron, thereby forming metastable iron sulfides (mackinawite, greigite) which are expected to transform into pyrite, the most thermodynamically stable phase. However, our understanding of this process mostly stems from pure cultures grown on sulfate, which fails to capture the complexity of natural microbial communities and subsequent sedimentary changes. To this end, we set up pure and co-culture incubations of sulfate- and sulfur-reducing bacteria with selected ferric minerals (goethite, ferric phosphate and ferrihydrite) or ferrous iron and later subjected the samples to experimental diagenesis at controlled temperature (80 degrees C). We hypothesized that the co-culture would enhance pyrite formation by maintaining an internal cryptic S cycle that replenishes polysulfides and ferrous iron via the sulfidation of ferric compounds. Our findings showed that iron sulfide morphology was strongly dependent on the reactivity of ferric compounds, rather than the presence of bacteria. Consistent with this, pyrite formed through diagenesis in both pure cultures and abiotic incubations amended with sodium sulfide, indicating that pyritization is a primarily chemically controlled process. Contrary to our expectations, the presence of the co-culture led to longer diagenetic preservation of metastable minerals like greigite and marcasite, ultimately hindering pyritization. Surprisingly, we could also detect spherulitic pyrite after experimental diagenesis in sterile samples without exogenous sulfide addition. This was explained by the abiotic disproportionation of elemental S which took place in temperature regimes usually associated with microbial sulfide production. Overall, these results highlight the influence of mixed microbial communities, but also overlooked abiotic reactions, on iron sulfide (trans)formations in sedimentary environments, with implications for paleo(magnetic) reconstructions and the usability of these minerals as biosignatures.

microbiology↗

The interplay between light, arsenic and H2O2 controls oxygenic photosynthesis in a Precambrian analog cyanobacterial mat.

The delayed rise of atmospheric oxygen, despite the early evolution of oxygenic photosynthesis (OP), remains a central puzzle in Earth history. Numerous ecological and geochemical constraints on OP have been proposed, but the role of environmental stressors at the physiological and ecosystem level is poorly understood. Here we show that Chl-f-harboring cyanobacteria in a high-altitude Andean microbial mat - an analog for Precambrian ecosystems - switch from OP to arsenite-driven anoxygenic photosynthesis (AP) under high light. Using microsensor profiling, mat incubations, and metatranscriptomics, we show that this shift is triggered by the accumulation of reactive oxygen species (ROS), especially hydrogen peroxide, which suppresses OP. Instead of ceasing activity, cyanobacteria reroute electron flow, using arsenite as the electron donor to sustain photosynthesis while avoiding both intracellular ROS from OP and extracellular ROS from aerobic arsenite oxidation. This switch is reversible and coordinated with diel cycles of light and arsenic speciation, sustained by a cryptic arsenic redox cycle, continuously regenerating arsenite for AP. Although the enzymatic basis remains unresolved, these findings reveal a hidden layer of metabolic plasticity in cyanobacteria and suggest that oxidative stress-responsive metabolic shifts may have supported early phototroph survival while limiting oxygen release - potentially contributing to Earths protracted oxygenation.

biochemistry↗