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Antler is a kind of natural biological material that is an important weapon for attack and defense and has good strength and excellent toughness. Synchrotron radiation computed tomography technology was adopted in this paper to continuously observe the deformation and failure process of the internal microstructure of antlers during the tensile process. The corresponding full-field strain and evolution of information of the internal structure were quantitatively analyzed combined with digital volume correlation technology. In the experiment, a large quantity of internal canals and lacunae with various shapes and sizes, forming a complex 3D spatial arrangement in antlers, were observed. While realizing the overall lightweight design of the structure, these pore structures can also implement a decrease in local strain concentration and block the long-distance propagation of the high strain concentration region through their cooperation and respective advantages. In addition, there are special high shear strain distribution regions in the antler, which guide the frequent deflection and stepped expansion of cracks, thus playing an important role in the excellent load-bearing capacity and energy dissipation of the antler. These results have positive guiding significance for the lightweight design and performance optimization of artificial porous materials.

The unique proline isomerase Pin1 is pivotal for protecting against age-dependent neurodegeneration in Alzheimer's disease (AD), with its inhibition providing a molecular link between tangle and plaque pathologies. Pin1 is oxidatively modified in human AD brains, but little is known about its regulatory mechanisms and pathological significance of such Pin1 modification. In this paper, our determination of crystal structures of oxidized Pin1 reveals a series of Pin1 oxidative modifications on Cys113 in a sequential fashion. Cys113 oxidization is further confirmed by generating antibodies specifically recognizing oxidized Cys113 of Pin1. Furthermore, Pin1 oxidation on Cys113 inactivates its catalytic activity in vitro, and Ala point substitution of Cys113 inactivates the ability of Pin1 to isomerize tau as well as to promote protein turnover of tau and APP. Moreover, redox regulation affects Pin1 subcellular localization and Pin1-mediated neuronal survival in response to hypoxia treatment. Importantly, Cys113-oxidized Pin1 is significantly increased in human AD brain comparing to age-matched controls. These results not only identify a novel Pin1 oxidation site to be the critical catalytic residue Cys113, but also provide a novel oxidative regulation mechanism for inhibiting Pin1 activity in AD. These results suggest that preventing Pin1 oxidization might help to reduce the risk of AD.

The effective elimination of aromatic compounds from wastewater is imperative for safeguarding the ecological environment. Bioelectrochemical processes that combine cathodic reduction and anodic oxidation represent a promising approach for the biomineralization of aromatic compounds. However, conventional direct current bioelectrochemical methods have intrinsic limitations. In this study, a low-frequency and low-voltage alternating current (LFV-AC)-driven bioelectrode offering periodic in situ coupling of reduction and oxidation processes was developed for the biomineralization of aromatic compounds, as exemplified by the degradation of alizarin yellow R (AYR). LFV-AC stimulated biofilm demonstrated efficient bidirectional electron transfer and oxidation–reduction bifunctionality, considerably boosting AYR reduction (63.07% ± 1.91%) and subsequent mineralization of intermediate products (98.63% ± 0.37%). LFV-AC stimulation facilitated the assembly of a collaborative microbiome dedicated to AYR metabolism, characterized by an increased abundance of functional consortia proficient in azo dye reduction (Stenotrophomonas and Bradyrhizobium), aromatic intermediate oxidation (Sphingopyxis and Sphingomonas), and electron transfer (Geobacter and Pseudomonas). The collaborative microbiome demonstrated a notable enrichment of functional genes encoding azo- and nitro-reductases, catechol oxygenases, and redox mediator proteins. These findings highlight the effectiveness of LFV-AC stimulation in boosting azo dye biomineralization, offering a novel and sustainable approach for the efficient removal of refractory organic pollutants from wastewater.

Polyethylene terephthalate (PET), one of the most ubiquitous engineering plastics, presents both environmental challenges and opportunities for carbon neutrality and a circular economy. This review comprehensively addressed the latest developments in biotic and abiotic approaches for PET recycling/upcycling. Biotically, microbial depolymerization of PET, along with the biosynthesis of reclaimed monomers [terephthalic acid (TPA), ethylene glycol (EG)] to value-added products, presents an alternative for managing PET waste and enables CO2 reduction. Abiotically, thermal treatments (i.e., hydrolysis, glycolysis, methanolysis, etc.) and photo/electrocatalysis, enabled by catalysis advances, can depolymerize or convert PET/PET monomers in a more flexible, simple, fast, and controllable manner. Tandem abiotic/biotic catalysis offers great potential for PET upcycling to generate commodity chemicals and alternative materials, ideally at lower energy inputs, greenhouse gas emissions, and costs, compared to virgin polymer fabrication. Remarkably, over 25 types of upgraded PET products (e.g., adipic acid, muconic acid, catechol, vanillin, and glycolic acid, etc.) have been identified, underscoring the potential of PET upcycling in diverse applications. Efforts can be made to develop chemo-catalytic depolymerization of PET, improve microbial depolymerization of PET (e.g., hydrolysis efficiency, enzymatic activity, thermal and pH level stability, etc.), as well as identify new microorganisms or hydrolases capable of degrading PET through computational and machine learning algorithms. Consequently, this review provides a roadmap for advancing PET recycling and upcycling technologies, which hold the potential to shape the future of PET waste management and contribute to the preservation of our ecosystems.

In environmental matrices, the migration and distribution of contaminants at water–solid interfaces play a crucial role in their capture or dissemination. Scientists working in environmental remediation and wastewater treatment are increasingly aware of metal–contaminant coordination; however, interfacial behaviors remain underexplored. Here, we show that trivalent metal ions (e.g. Al3+ and Fe3+) mediate the migration of pollutant ligands (e.g. tetracycline (TC) and ofloxacin) to the organic solid interface. In the absence of Al3+, humic acid (HA) colloids (50 mg/L) capture 26.1 % of the TC in water (initial concentration: 10 mg/L) via weak intermolecular interactions (binding energy: −5.71 kcal/mol). Adding Al3+ (2.5 mg/L) significantly enhances the binding of TC to an impressive 94.2 % via Al3+ mediated coordination (binding energy: −84.89 kcal/mol). The significant increase in binding energy results in superior interfacial immobilization. However, excess free Al3+ competes for TC binding via direct binary coordination, as confirmed based on the unique fluorescence of Al3+–TC complexes. Density functional theory calculations reveal the intricate process of HA–Al3+ binding via carboxyl and phenolic hydroxyl sites. The HA–Al3+ flocs then leverage the remaining coordination capacity of Al3+ to chelate with TC. As well as providing insights into the pivotal role of metal ion on the self-purification of natural water bodies, our findings on the interfacial behavior of metal–contaminant coordination will propel coagulation technology to the capture of microscale pollutants.

Electrode biofilm and planktonic microorganisms are two important parts in bioelectrochemical system, but the mechanism of planktonic microorganisms affect biofilms is not clear. Waste sludge lysate produced from sludge pyrolysis contains melanoidins as complex carbon source that are refractory. Anaerobic digestion companied with weak electrostimulation is adopted to treat the wastewater and explore the mechanism in electron transfer, biofilm activity and microbial community structure. In the presence of planktonic microorganisms, electrode biofilm still plays a major role that about 70% of organics was removed by biofilm, the energy recovery efficiency increased by 10.81%, and the main electron transfer mechanism of biofilm is unchanged, but extra electron transfer pathway (Ef = 0.404 V vs Ag/AgCl) is generated. More cytochrome is produced in biofilm and charge transfer resistance decreases to facilitate electron transfer. The planktonic microorganisms cause more electrochemically active microorganisms and methanogens enrich in the electrode biofilm to enhance the direct interspecies electron transfer.

Carbon cycle regulation and greenhouse gas (GHG) emission abatement within wastewater treatment plants (WWTPs) can theoretically improve sustainability. Currently, however, large amounts of external carbon sources used for deep nitrogen removal and waste sludge disposal aggravate the carbon footprint of most WWTPs. In this pilot-scale study, considerable carbon was preliminarily recovered from primary sludge (PS) through short-term (five days) acidogenic fermentation and subsequently utilized on-site for denitrification in a wool processing industrial WWTP. The recovered sludge-derived carbon sources were excellent electron donors that could be used as additional carbon supplements for commercial glucose to enhance denitrification. Additionally, improvements in carbon and nitrogen flow further contributed to GHG emission abatement. Overall, a 9.1% reduction in sludge volatile solids was achieved from carbon recovery, which offset 57.4% of external carbon sources, and the indirect GHG emissions of the target industrial WWTP were reduced by 8.05%. This study demonstrates that optimizing the allocation of carbon mass flow within a WWTP has numerous benefits.

Anaerobic digestion (AD) of organics is a challenging task under high-strength sulfate (SO42−) conditions. The generation of toxic sulfides by SO42−-reducing bacteria (SRB) causes low methane (CH4) production. This study investigated the feasibility of alleviating sulfide inhibition and enhancing CH4 production by using an anaerobic reactor with built-in microbial electrolysis cell (MEC), namely ME-AD reactor. Compared to AD reactor, unionized H2S in the ME-AD reactor was sufficiently converted into ionized HS− due to the weak alkaline condition created via cathodic H2 production, which relieved the toxicity of unionized H2S to methanogenesis. Correspondingly, the CH4 production in the ME-AD system was 1.56 times higher than that in the AD reactor with alkaline-pH control and 3.03 times higher than that in the AD reactors (no external voltage and no electrodes) without alkaline-pH control. MEC increased the amount of substrates available for CH4-producing bacteria (MPB) to generate more CH4. Microbial community analysis indicated that hydrogentrophic MPB (e.g. Methanosphaera) and acetotrophic MPB (e.g. Methanosaeta) participated in the two major pathways of CH4 formation were successfully enriched in the cathode biofilm and suspended sludge of the ME-AD system. Economic revenue from increased CH4 production totally covered the cost of input electricity. Integration of MEC with AD could be an attractive technology to alleviate sulfide inhibition and enhance CH4 production from AD of organics under SO42−-rich condition. Keywords: Anaerobic digestion (AD), Methanogenesis, Sulfate reduction, Microbial electrolysis, Microbial community analysis