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To enhance the contaminant removal efficiency of the electro-Fenton (E-Fenton) process, a nitrogen and phosphorus co-doped graphite felt (NPGF) cathode was synthesized using an anodic oxidation technique. An ascorbic acid-coupled NPGF E-Fenton system was then established for the degradation of ciprofloxacin (CIP). The NPGF cathode featured abundant oxygen-containing functional groups (such as -COOH and -OH), which enhanced the selectivity of oxygen reduction and facilitated the formation of H 2 O 2 . The introduction of N and P doping disrupted the charge balance within the carbon framework, accelerating electron transfer. Together, the NPGF electrode and ascorbic acid enhanced the cycling of Fe 3+ /Fe 2+ while preventing the formation of iron sludge. Under optimal conditions (ascorbic acid concentration of 0.3 mM, current density of 2.0 mA cm -2 , pH of 3.0, aeration rate of 0.6 L min -1 , and Fe 2+ concentration of 0.2 mM), CIP was completely removed within 20 min. The NPGF electrode exhibited excellent stability, maintaining 95.35% CIP removal even after 8 cycles. Analysis revealed that singlet oxygen primarily mediated the degradation of CIP, with its concentration measured at 1.23 × 10 -7 M. Density functional theory was used to analyze the characteristics and potential attack sites of CIP, enabling the proposal of plausible degradation pathways. Toxicity simulations and Escherichia coli growth inhibition experiments demonstrated a reduction in the toxicity of CIP and its intermediate products. This study offers a valuable reference for improving the efficiency of E-Fenton technology in antibiotic wastewater treatment., Competing Interests: Declaration of Competing Interest ☒ The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Inc.)

Mixed forests generally have a higher carbon sequestration potential than pure forests. However, the effects of different types of mixed afforestation on soil organic carbon (SOC) and its labile fractions still remain controversial. We examined the concentrations of each SOC labile fraction at 0-50 cm soil depth, understory plant communities, stand plant biomass and studied their integrated effects on soil carbon stocks in three types of Pinus massoniana afforestation: a monoculture (MPF), a mixed forest with Cunninghamia lanceolata (MCLMF) and a mixed forest with Liquidambar formosana (MLMF). The results showed that the SOC stocks, i.e., concentrations of SOC and its labile fractions, across soil depths in all three afforestation types decreased with soil depth and ranked in the following order: MCLMF > MPF > MLMF. The concentrations of SOC and its labile fractions displayed a significant positive correlation with the diversity and biomass of understory plants and a significant negative correlation with tree biomass. The MCLMF had the largest SOC stocks (83.45 ± 7.59 Mg ha -1 ) and the smallest aboveground plant biomass carbon stocks (85.2 ± 4.07 Mg ha -1 ), while those of the MLMF were the opposite (SOC stocks, 35.63 ± 4.47 Mg ha -1 ; plant biomass carbon stocks, 144.28 ± 1.19 Mg ha -1 ). The forest carbon stocks (comprising both SOC and plant biomass carbon pools) were ranked as MLMF > MCLMF > MPF. Our results revealed that the diversity and biomass of understory plants can improve the stocks of SOC and its labile fractions, whereas trees may weaken the role of understory plants. In this sense, the diversity and biomass of understory plants should be emphasized in the process of mixed afforestation, especially mixed broadleaf-conifer afforestation, to increase SOC sequestration., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Clay minerals formations are potential geological barrier (host rocks) for the long-rerm storage of uranium tailing in deep geological repositories. However, there are still obstacles to the efficient retardation of uranium because of the competition between negatively charged regions at the clay minerals end face, surface and between layers, as well as low mineralization capacity. Herein, employing a simple method, we used sodium alginate (SA), an inexpensive natural polymer material, polyethylene (PE), and the natural clay minerals montmorillonite (Mt), nontronite (Nt), and beidellite (Bd) to prepare three hydrogel adsorbents, (denoted as Mt/PE-@SA, Nt/PE-@SA, and Bd/PE-@SA), respectively. The application of obtained hydrogel adsorbents further extends to uranium(VI) removal from aqueous. Due to the synergistic action of SA group and PE group, hydrogel adsorbents showed select adsorption and mineralization effect on uranium(VI), among which the maximum uranium(VI) adsorption capacity of Nt/PE-@SA was 133.3 mg·g -1 and Mt/PE-@SA exhibited strong selectivity for uranium(VI) in the presence of coexisting metal ions. Cyclic voltammetry studies indicated the mitigation and immobilization of uranium species onto adsorbents by both reduction and mineralization. Besides, the synergistic adsorption of SA and PE on clay minerals was hypothesized, and the idea was supported by structure optimizations results from Monte Carlo dynamics simulation (MCD). Three obtained hydrogel adsorbents structural model was constructed based on its physicochemical characterization, the low energy adsorption sites and adsorption energies are investigated using MCD simulation. The simulation results show that obtained hydrogel adsorbents have a strong interaction with uranium(VI), which ensures the high adsorption capacity of those materials. Most importantly, this work demonstrates a new strategy for preparing mineral-based hydrogel adsorbents with enough stability and provides a new perspective for uranium(VI) removal in complex environment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Background Aims: Stem cell therapy is a novel therapy being explored for AD. The molecular mechanism of its effect is still unclear. The authors investigated the effects and mechanism by injection of SHEDs into an AD mouse model., Methods: SHEDs were cultured in vitro and injected into AD SAMP8 mice by caudal vein, and SHEDs labeled via synthetic dye showed in vivo migration to the head. The cognitive ability of SAMP8 mice was evaluated via Barnes maze and new object recognition. The pathological indicators of AD, including Tau, amyloid plaques and inflammatory factors, were examined at the protein or RNA level. Next, macro-proteomics analysis and weighted gene co-expression network analysis (WGCNA) based on protein groups and behavioral data were applied to discover the important gene cluster involved in the improvement of AD by SHEDs, which was further confirmed in an AD model in both mouse and cell lines., Results: SHED treatment improved the cognitive ability and pathological symptoms of SAMP8 mice. Proteomics analysis indicated that these improvements were tightly related to the mitochondria, which was proved through examination of the shape and function of mitochondria both in vivo (SAMP8 brain) and in vitro (SH-SY5Y cells). Finally, the core targets of SHEDs in the mitochondrial pathway, Hook3, Mic13 and MIF, were screened out and confirmed in vivo., Conclusions: SHED treatment significantly relieved AD symptoms, improved cognitive ability and reversed memory loss in an AD mouse model, possibly through the recovery of dysfunctional mitochondria. These results raise the possibility that SHED may ease the symptoms of AD by targeting the mitochondria., Competing Interests: Declaration of Competing Interest The authors have no commercial, proprietary or financial interest in the products or companies described in this article., (Copyright © 2021 International Society for Cell & Gene Therapy. Published by Elsevier Inc. All rights reserved.)

Cd contamination in rice grains has become a topic of great concern because of the high health risks associated with the long-term consumption of Cd-contaminated rice. Identification of Cd sources in rice grains by scientific methods is important for controlling heavy metal pollution and protecting human health. Here, the Cd concentrations and Cd isotopic compositions of rice plants (root, stem, leaf, and grain) and topsoil, and possible pollution sources (agricultural fertilizers, industrial dust, and automobile exhaust) were analyzed using an instrument of inductively coupled plasma mass spectrometry (ICP-MS) and multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS). The results showed variations in the Cd isotopes of different components of rice plants and the fractionation coefficient of rice grains relative to topsoil (Δ 114/110 Cd rice grains-topsoil = 0.25‰). The contributions of pollution sources to rice grains were realized by combining the Cd isotopic composition with an isotopic mixing model (Isosource). The analysis showed that all three possible pollution sources contributed to the Cd in the rice grains in the field, the average Cd contribution of industrial dust, agricultural fertilizers and automobile exhaust was 87%, 9%, and 4%, respectively. Our study provides a feasible method for the identification of pollution sources of Cd in rice grains at the field scale and demonstrates that Cd isotopic composition is one of the powerful tools to trace the pollution sources of Cd in crops., (Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.)

Enteromorpha prolifera (EP) biomass collected from a lake in China was employed for biochar production. The EP biochar was magnetically modified by loading γ-Fe 2 O 3 particles on the surface, and Cr(VI) adsorption behavior and mechanism were evaluated. The magnetic biochar had higher surface polarity, specific surface area and exhibited a higher Cr(VI) adsorption capacity of 95.23 mg/g biochar compared with pristine EP biochar. The pronounced electron spin resonance (ESR) signals showed that the environmental persistent free radicals (EPFRs) preferred to form at lower pyrolysis temperature and lower transition metal concentration. The g factors of BC400, BC800 and BCF400 were 1.8959, 1.7955 and 1.7954, respectively, indicating that the EPFRs mainly used carbon atom as center. In addition, biological toxicity of magnetic EP biochar was tested using the microalga Scenedesmus obliquus. Exposure of S. obliquus cells to magnetic biochar led to the accumulation of reactive oxygen species (ROS) and oxidative stress. The leaching solution toxicity of BCF400 was stronger than BCF800. Thus, the magnetic EP biochar prepared at higher temperature (such as BCF800) provide better Cr (VI) performance with low biologic toxicity. And the EP biomass could be a promising low-cost feedstock for biochar production., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Organic anion transporting polypeptide 1B1 (OATP1B1) is a key hepatic uptake transporter whose inhibition could lead to adverse drug-drug and drug-food interactions. Flavonoids are widely distributed in food and beverages and thus our bodies are frequently exposed to them. Therefore, investigation of the interactions between OATP1B1 and flavonoids could be of great significance. In the present study, 25 common flavonoids were investigated for their interactions with OATP1B1 using the fluorescent substrate 2',7'-dichlorofluorescein (DCF) and three-dimensional quantitative structure-activity relationship (3D-QSAR) analysis. Kinetic study showed that OATP1B1-mediated DCF uptake exhibited a monophasic saturation kinetics with a K m value of 9.7 ± 2.4 μM. Inhibition assay for flavonoids on OATP1B1-mediated DCF uptake was performed and their IC 50 values were determined upon which reliable and predictive CoMFA (q 2  = 0.604, r 2  = 0.841) and CoMSIA (q 2  = 0.534, r 2  = 0.807) models were developed. Our experimental and computational results showed that flavonoid aglycones interacted with OATP1B1 much stronger than their glycosides such as 3-O- and 7-O-glycosides as bulky hydrophilic and hydrogen-bond forming substituents at C-3 and C-7 positions on rings A and C were unfavorable for their binding. On the other hand, the presence of hydrogen-bond forming groups on ring B was beneficial as long as the number of hydroxyl groups was not >2. Our results also indicated that flavones usually interacted with OATP1B1 much stronger than their 3-hydroxyflavone counterparts (flavonols). The obtained information and 3D-QSAR models could be useful for elucidating and predicting the interactions between flavonoids and human OATP1B1., Competing Interests: Declaration of competing interest All authors declare no conflicts of interest., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Picornavirus replication is critically dependent on the correct processing of a polyprotein precursor by 3C protease(s) (3C(pro)) at multiple specific sites with related but non-identical sequences. To investigate the structural basis of its cleavage specificity, we performed the first crystallographic structural analysis of non-covalent complexes of a picornavirus 3C(pro) with peptide substrates. The X-ray crystal structure of the foot-and-mouth disease virus 3C(pro), mutated to replace the catalytic Cys by Ala and bound to a peptide (APAKQ|LLNFD) corresponding to the P5-P5' region of the VP1-2A cleavage junction in the viral polyprotein, was determined up to 2.5 A resolution. Comparison with free enzyme reveals significant conformational changes in 3C(pro) on substrate binding that lead to the formation of an extended interface of contact primarily involving the P4-P2' positions of the peptide. Strikingly, the deep S1' specificity pocket needed to accommodate P1'-Leu only forms when the peptide binds. Substrate specificity was investigated using peptide cleavage assays to show the impact of amino acid substitutions within the P5-P4' region of synthetic substrates. The structure of the enzyme-peptide complex explains the marked substrate preferences for particular P4, P2 and P1 residue types, as well as the relative promiscuity at P3 and on the P' side of the scissile bond. Furthermore, crystallographic analysis of the complex with a modified VP1-2A peptide (APAKE|LLNFD) containing a Gln-to-Glu substitution reveals an identical mode of peptide binding and explains the ability of foot-and-mouth disease virus 3C(pro) to cleave sequences containing either P1-Gln or P1-Glu. Structure-based mutagenesis was used to probe interactions within the S1' specificity pocket and to provide direct evidence of the important contribution made by Asp84 of the Cys-His-Asp catalytic triad to proteolytic activity. Our results provide a new level of detail in our understanding of the structural basis of polyprotein cleavage by 3C(pro)., (Copyright 2009 Elsevier Inc. All rights reserved.)