Irreversible Trace Metal Binding to Goethite Controlled by the Ion Size.

The dynamics of trace metals at mineral surfaces influence their fate and bioaccessibility in the environment. Trace metals on iron (oxyhydr)oxide surfaces display adsorption-desorption hysteresis, suggesting entrapment after aging. However, desorption experiments may perturb the coordination environment of adsorbed metals, the distribution of labile Fe(III), and mineral aggregation properties, influencing the interpretation of labile metal fractions. In this study, we investigated irreversible binding of nickel, zinc, and cadmium to goethite after aging times of 2-120 days using isotope exchange. Dissolved and adsorbed metal pools exchange rapidly, with half times <90 min, but all metals display a solid-associated fraction inaccessible to isotope exchange. The size of this nonlabile pool is the largest for nickel, with the smallest ionic radius, and the smallest for cadmium, with the largest ionic radius. Spectroscopy and extractions suggest that the irreversibly bound metals are incorporated in the goethite structure. Rapid exchange of labile solid-associated metals with solution demonstrates that adsorbed metals can sustain the dissolved pool in response to biological uptake or fluid flow. Trace metal fractions that irreversibly bind following adsorption provide a contaminant sequestration pathway, limit the availability of micronutrients, and record metal isotope signatures of environmental processes.

OAS3 Deubiquitination Due to E3 Ligase TRIM21 Downregulation Promotes Epithelial Cell Apoptosis and Drives Sepsis-induced Acute Lung Injury.

Patients with sepsis-induced acute lung injury (SALI) show a high mortality rate, and there is no effective treatment in the clinic for SALI but only symptomatic treatment as an option. Therefore, searching for effective targets is critical for the management of SALI. Ubiquitination is an essential post-translational protein modification involved in most pathophysiological processes. However, the relationship between ubiquitination and SALI remains largely unclear. In this study, we examined the ubiquitination modification changes in SALI, identified oligoadenylate synthetase 3 (OAS3) as a key candidate accounting for SALI from integrative multi-omics analysis and confirmed its role in promoting SALI and cell apoptosis in an animal model of cecal ligation and puncture-treated mice and a cellular model of LPS-treated MLE12 cells. Mechanistically, downregulation of E3 ligase TRIM21 mediates the reduction of OAS3 K48-linked polyubiquitination at the K1079 site in lung epithelial cells of a septic model, which leads to the increase of OAS3 protein level in a proteasomal-dependent manner. The upregulated OAS3 promotes epithelial cell apoptosis through its downstream effector molecule, RNase L. In summary, these findings unveil a previously unappreciated role of OAS3 ubiquitination in SALI and offer a promising perspective for further understanding the development of sepsis and potential therapeutic target for the treatment of SALI.

Organic Controls over Biomineral Ca-Mg Carbonate Compositions and Morphologies.

Calcium carbonate minerals, such as aragonite and calcite, are widespread in biomineral skeletons, shells, exoskeletons, and more. With rapidly increasing pCO2 levels linked to anthropogenic climate change, carbonate minerals face the threat of dissolution, especially in an acidifying ocean. Given the right conditions, Ca-Mg carbonates (especially disordered dolomite and dolomite) are alternative minerals for organisms to utilize, with the added benefit of being harder and more resistant to dissolution. Ca-Mg carbonate also holds greater potential for carbon sequestration due to both Ca and Mg cations being available to bond with the carbonate group (CO32-). However, Mg-bearing carbonates are relatively rare biominerals because the high kinetic energy barrier for the dehydration of the Mg2+-water complex severely restricts Mg incorporation in carbonates at Earth surface conditions. This work presents the first overview of the effects of the physiochemical properties of amino acids and chitins on the mineralogy, composition, and morphology of Ca-Mg carbonates in solutions and on solid surfaces. We discovered that acidic, negatively charged, hydrophilic amino acids (aspartic and glutamic) and chitins could induce the precipitation of high-magnesium calcite (HMC) and disordered dolomite in solution and on solid surfaces with these adsorbed biosubstrates via in vitro experiments. Thus, we expect that acidic amino acids and chitins are among the controlling factors in biomineralization used in different combinations to control the mineral phases, compositions, and morphologies of Ca-Mg carbonate biomineral crystals.

Low-Temperature Synthesis of Disordered Dolomite and High-Magnesium Calcite in Ethanol-Water Solutions: The Solvation Effect and Implications.

How dolomite [CaMg(CO3)2] forms is still underdetermined, despite over a century of efforts. Challenges to synthesizing dolomite at low temperatures have hindered our understanding of sedimentary dolomite formation. Unlike calcium, magnesium's high affinity toward water results in kinetic barriers from hydration shells that prevent anhydrous Ca-Mg carbonate growth. Previous synthesis studies show that adding low-dielectric-constant materials, such as dioxane, dissolved sulfide, and dissolved silica, can catalyze the formation of disordered dolomite. Also, polar hydrophilic amino acids and polysaccharides, which are very common in biomineralizing organisms, could have a positive role in stimulating Mg-rich carbonate precipitation. Here, we show that disordered dolomite and high-magnesium calcite can be precipitated at room temperature by partially replacing water with ethanol (which has a lower dielectric constant) and bypassing the hydration barrier. Increasing the ethanol volume percentage of ethanol results in higher Mg incorporation into the calcite structure. When the ethanol volume percentage increases to 75 vol %, disordered dolomite (>60 mol % MgCO3) can rapidly precipitate from a solution with [Mg2+] and [Ca2+] mimicking seawater. Thus, our results suggest that the hydration barrier is the critical kinetic inhibitor to primary dolomite precipitation. Ethanol synthesis experiments may provide insights into other materials that share similar properties to promote high-Mg calcite precipitation in sedimentary and biomineral environments.

Microbial chemolithotrophic oxidation of pyrite in a subsurface shale weathering environment: Geologic considerations and potential mechanisms.

Oxidative weathering of pyrite plays an important role in the biogeochemical cycling of Fe and S in terrestrial environments. While the mechanism and occurrence of biologically accelerated pyrite oxidation under acidic conditions are well established, much less is known about microbially mediated pyrite oxidation at circumneutral pH. Recent work (Percak-Dennett et al., 2017, Geobiology, 15, 690) has demonstrated the ability of aerobic chemolithotrophic microorganisms to accelerate pyrite oxidation at circumneutral pH and proposed two mechanistic models by which this phenomenon might occur. Here, we assess the potential relevance of aerobic microbially catalyzed circumneutral pH pyrite oxidation in relation to subsurface shale weathering at Susquehanna Shale Hills Critical Zone Observatory (SSHCZO) in Pennsylvania, USA. Specimen pyrite mixed with native shale was incubated in groundwater for 3 months at the inferred depth of in situ pyrite oxidation. The colonized materials were used as an inoculum for pyrite-oxidizing enrichment cultures. Microbial activity accelerated the release of sulfate across all conditions. 16S rRNA gene sequencing and metagenomic analysis revealed the dominance of a putative chemolithoautotrophic sulfur-oxidizing bacterium from the genus Thiobacillus in the enrichment cultures. Previously proposed models for aerobic microbial pyrite oxidation were assessed in terms of physical constraints, enrichment culture geochemistry, and metagenomic analysis. Although we conclude that subsurface pyrite oxidation at SSCHZO is largely abiotic, this work nonetheless yields new insight into the potential pathways by which aerobic microorganisms may accelerate pyrite oxidation at circumneutral pH. We propose a new "direct sulfur oxidation" pathway, whereby sulfhydryl-bearing outer membrane proteins mediate oxidation of pyrite surfaces through a persulfide intermediate, analogous to previously proposed mechanisms for direct microbial oxidation of elemental sulfur. The action of this and other direct microbial pyrite oxidation pathways have major implications for controls on pyrite weathering rates in circumneutral pH sedimentary environments where pore throat sizes permit widespread access of microorganisms to pyrite surfaces.

Biomineral armor in leaf-cutter ants.

Although calcareous anatomical structures have evolved in diverse animal groups, such structures have been unknown in insects. Here, we report the discovery of high-magnesium calcite [CaMg(CO3)2] armor overlaying the exoskeletons of major workers of the leaf-cutter ant Acromyrmex echinatior. Live-rearing and in vitro synthesis experiments indicate that the biomineral layer accumulates rapidly as ant workers mature, that the layer is continuously distributed, covering nearly the entire integument, and that the ant epicuticle catalyzes biomineral nucleation and growth. In situ nanoindentation demonstrates that the biomineral layer significantly hardens the exoskeleton. Increased survival of ant workers with biomineralized exoskeletons during aggressive encounters with other ants and reduced infection by entomopathogenic fungi demonstrate the protective role of the biomineral layer. The discovery of biogenic high-magnesium calcite in the relatively well-studied leaf-cutting ants suggests that calcareous biominerals enriched in magnesium may be more common in metazoans than previously recognized.