Development of novel bisphenol derivatives with a membrane-targeting mechanism as potent gram-positive antibacterial agents.

Antibiotic resistance is becoming increasingly severe. The development of small molecular antimicrobial peptides is regarded as a promising design strategy for antibiotics. Here, a series of bisphenol derivatives with amphiphilic structures were designed and synthesized as antibacterial agents by imitating the design strategy of antimicrobial peptides. After a series of structural optimizations, lead compound 43 was identified, which exhibited excellent antibacterial activity against Gram-positive bacterial strains (MICs = 0.78-1.56 µg/mL), poor hemolytic activity (HC50 > 200 µg/mL), and low cytotoxicity (CC50 > 100 µg/mL). Further biological evaluation results indicated that 43 exerted antibacterial effects by directly destroying bacterial cell membranes and displayed rapid bactericidal properties (within 0.5-1 h), leading to a very low probability of drug resistance. Moreover, in a murine model of corneal infection, 43 exhibited a strong in vivo antibacterial efficacy. These findings indicate that 43 is a promising candidate compound for the treatment of bacterial infections.

Sulfite-Assisted Acetate Conversion from CO Electroreduction.

The efficient acetate conversion from CO electroreduction is challenging due to the poor selectivity at high reaction rate, which requires the competition with H2 and other C2+ (i.e., ethylene, ethanol, n-propanol) reduction products. Electrolyte engineering is one of the efficient strategies to regulate the reaction microenvironment. In this work, the adding of sulfite (SO32-) with high nucleophilicity in KOH electrolytes was demonstrated to enable improving the CO-to-acetate conversion via generating a S-O chemical bond between SO32- and oxygenated *C2 intermediates (i.e., *CO-CO, *CO-COH) compared with that in pure KOH system on both synthesized Cu(200)- and normal commercial Cu(111)-facets-exposed metallic Cu catalysts. As a result, the prepared Cu(200)-facets-exposed metallic Cu catalyst with surface ions modification showed an superior Faradaic efficiency of 63.6% at -0.6 A·cm-2, and extraordinary absolute value of peak partial current density as high as 1.52 A·cm-2 with adding SO32- in KOH electrolytes, compared to the best reported values in both CO and CO2 electroreduction. Our work suggests an attractive strategy to introduce the oxyanion with high nucleophilicity in electrolytes to regulate the microenvironment for industrial-current-density electrosynthesis of acetate from CO electroreduction.

Valence-Dependent Implicit Action Generalization Among Group Members.

People implicitly generalize the actions of known individuals in a social group to unknown members. However, actions have social goals and evaluative valences, and the extent to which actions with different valences (helpful and harmful) are implicitly generalized among group members remains unclear. We used computer animations to simulate social group actions, where helping and hindering actions were represented by aiding and obstructing another's climb up a hill. Study 1 found that helpful actions are implicitly expected to be shared among members of the same group but not among members of different groups, but no such effect was found for harmful actions. This suggests that helpful actions are more likely than harmful actions to be implicitly generalized to group members. This finding was replicated in Study 2 by increasing the group size from three to five. Study 3 found that the null effect for generalizing harmful actions among group members is not due to the difficulty of detecting action generalization, as both helpful and harmful actions are similarly generalized within particular individuals. Moreover, Study 4 demonstrated that weakening social group information resulted in the absence of implicit generalization for helpful actions, suggesting the specificity of group membership. Study 5 revealed that the generalization of helping actions occurred when actions were performed by multiple group members rather than being repeated by one group member, showing group-based inductive generalization. Overall, these findings support valence-dependent implicit action generalization among group members. This implies that people may possess different knowledge regarding valenced actions on category-based generalization.

Hierarchical Porous Aerogels With Multiple Adsorptive Interactions for Dye Wastewater Purification.

Aerogels present a huge potential for removing organic dyes from printing and dyeing wastewater (PDW). However, the preparation of aerogels with multiple dye adsorption capabilities remains a challenge, as many existing aerogels are limited to adsorbing only a single type of dye. Herein, a composite aerogel (CG/T-rGO) with the addition of carboxymethyl chitosan, gelatin and tannic acid reduced graphene oxide (T-rGO) was synthesized by freeze-drying technology. The electrostatic interactions between dye molecular and GEL/CMCS (CG) networks, as well as the supramolecular interactions (H-bonds, electrostatic interactions and π-π stacks) between T-rGO, have endowed the aerogel with the ability to adsorb multiple types of dye, such as methylene blue (MB) and methyl orange (MO). Results exhibited that the prepared CG/T-rGO aerogel possessed strong mechanical strength and a porous 3D network structure with a porosity of 96.33 %. Using MB and MO as adsorbates, the adsorption capacity (88.2 mg/g and 66.6 mg/g, respectively) and the mechanism of the CG/T-rGO aerogel were investigated. The adsorption processes of aerogel for MB and MO were shown to follow the pseudo-second-order kinetic model and Langmuir isotherm model, indicating the chemical adsorption of a monolayer. The proposed aerogel in this work has promising prospects for dye removal from PDW.

Phosphorus partitioning contribute to phosphorus use efficiency during grain filling in Zea mays.

Introduction: Lower phosphorus (P) availability limits crop productivity in agroecosystems. The remobilization of P from the source to the sink organs plays an important role in enhancing the P-utilization efficiency of crops. During the grain filling stage, phosphorus flow to the developing grains, the primary sink, determines crop yield. However, the specific contributions of different organs to grain P throughout the post-silking period in maize remain unclear. Methods: In our study, three maize inbred lines (CIMBL89, Ji846, and CML118) with contrasting P statuses were selected and grown in a field with high P (HP, 150 kg ha-1 P2O5) and low P (LP, 0 kg ha-1 P2O5) conditions. Results: The grain yield of CIMBL89 was 69% and 169% greater under HP supply, and 83% and 309% greater than those of Ji846 and CML118 under LP supply, respectively. The ear length, ear diameter, and kernel row number of CML118 were lower than those of CIMBL89 and Ji846 under HP conditions. Most of the P (87%) in the grains of CIMBL89 came from P uptake at the LP supply, while almost all P (95%) came from P remobilization in various organs at the HP supply after silking. In contrast, 91% of the P found in the grain of CML118 came from P remobilization under LP supply, while 76% came from P uptake under HP supply after silking. Discussion: In conclusion, our findings suggest that CIMBL89, with greater P acquisition efficiency, contributes to grain formation and production during the post-silking period under LP conditions. Additionally, CIMBL89 can fully remobilize P and avoid the extravagant absorption of P in P-sufficient soil, which sets it apart from Ji846 and CML118.

The Severity of Cyberbullying Affects Bystander Intervention Among College Students: The Roles of Feelings of Responsibility and Empathy.

Background: Bystander intervention can protect victims from harm in cyberbullying. Previous studies have found that the severity of cyberbullying incidents is one of the important factors affecting decisions to intervene. However, little is known about the mediating and moderating mechanisms underlying this effect. Purpose: The current study explored the effect of the severity of cyberbullying incidents on bystander intention to intervene on social network sites (SNSs) among college students (Experiment 1), the mediating role of feelings of responsibility (Experiment 2) and the moderating role of empathy (Experiment 3). Patients and Methods: We presented cyberbullying incidents with different levels of severity through scenarios including fictive Weibo news reports and comments. Participants were exposed to a fictive cyberbullying incident and asked to complete a questionnaire including measures of the variables of interest. Results: Our results showed that the severity of incidents positively affected bystander intention to intervene through the mediation of feelings of responsibility. Empathy moderated the effect of incident severity on bystander intention to intervene. Conclusion: The results of the current study help to understand the behavior of bystanders in cyberbullying and they provide a practical reference for intervention in cyberbullying incidents.

Coupling Value-Added Anodic Reactions with Electrocatalytic CO2 Reduction.

Electrocatalytic CO2 reduction features a promising approach to realize carbon neutrality. However, its competitiveness is limited by the sluggish oxygen evolution reaction (OER) at anode, which consumes a large portion of energy. Coupling value-added anodic reactions with CO2 electroreduction has been emerging as a promising strategy in recent years to enhance the full-cell energy efficiency and produce valuable chemicals at both cathode and anode of the electrolyzer. This review briefly summarizes recent progresses on the electrocatalytic CO2 reduction, and the economic feasibility of different CO2 electrolysis systems is discussed. Then a comprehensive summary of recent advances in the coupled electrolysis of CO2 and potential value-added anodic reactions is provided, with special focus on the specific cell designs. Finally, current challenges and future opportunities for the coupled electrolysis systems are proposed, which are targeted to facilitate progress in this field and push the CO2 electrolyzers to a more practical level.

Alginate foam gel modified by graphene oxide for wound dressing.

Recently, hydrogel dressings have been rapidly developed for wound healing. However, it is still a huge challenge to endow hydrogel wound dressings with excellent hemostatic performance. Here, a new wound treatment material, foam gel wound dressing, is reported, which possesses rapid hemostasis and antibacterial properties. The foam gel dressing is composed of chitooligosaccharide modified graphene oxide (CG) nanocomposites and calcium alginate foam substrate. In this system, CG has a strong interaction with platelets, which is helpful for rapid hemostasis. So the wound dressing could stop bleeding quickly within 10 s. Meanwhile, CG also provides excellent antibacterial properties to dressings, which is conducive to wound healing. Full-thickness wound healing experiments showed that compared with blank control and CG-free foam gel dressings, CG-loaded foam gel dressings shows better healing properties, and the wounds covered with them are almost completely healed within 12 days. In addition, histological morphology analysis displays CG-loaded wound dressing could significantly accelerate wound healing by reducing the inflammatory response and promoting vascular remodeling. This unique strategy provides a simple and practical method for the clinical application of the next generation of wound dressings.

Biocompatible Carboxymethyl Chitosan/GO-Based Sponge to Improve the Efficiency of Hemostasis and Wound Healing.

Sponges with highly absorptive properties have been widely used in emergency hemostasis. Graphene oxide (GO) has been extensively investigated in biomedical applications and is a promising candidate for hemostatic sponges. However, GO has been demonstrated to have adverse effects on the human body. To overcome this problem, a hemostatic sponge based on modified GO and carboxymethyl chitosan (CMCS) is successfully prepared, which has excellent water absorption ability and mechanical strength. Importantly, hemostasis assays showed that the composite sponge exhibited high hemostatic efficiency, and the possible hemostatic mechanism is also discussed in this study. Moreover, the results of in vitro antibacterial tests reveal that the composite sponge also presents strong antimicrobial effects against Staphylococcus aureus and Escherichia coli. Significantly, the composited sponge used as hemostatic dressing can effectively promote cell proliferation, achieving a wound closure rate of 95% on day 12. Such a graphene-based sponge with multiple advantageous features would hold broad prospects in the hemostatic field.

Combining analyses of metabolite profiles and phosphorus fractions to explore high phosphorus utilization efficiency in maize.

Phosphorus (P) limitation is a significant factor restricting crop production in agricultural systems, and enhancing the internal P utilization efficiency (PUE) of crops plays an important role in ensuring sustainable P use in agriculture. To better understand how P is remobilized to affect crop growth, we first screened P-efficient (B73 and GEMS50) and P-inefficient (Liao5114) maize genotypes at the same shoot P content, and then analyzed P pools and performed non-targeted metabolomic analyses to explore changes in cellular P fractions and metabolites in maize genotypes with contrasting PUE. We show that lipid P and nucleic acid P concentrations were significantly lower in lower leaves of P-efficient genotypes, and these P pools were remobilized to a major extent in P-efficient genotypes. Broad metabolic alterations were evident in leaves of P-efficient maize genotypes, particularly affecting products of phospholipid turnover and phosphorylated compounds, and the shikimate biosynthesis pathway. Taken together, our results suggest that P-efficient genotypes have a high capacity to remobilize lipid P and nucleic acid P and promote the shikimate pathway towards efficient P utilization in maize.

Lithium Vacancy-Tuned [CuO4 ] Sites for Selective CO2 Electroreduction to C2+ Products.

Electrochemical CO2 reduction to valuable multi-carbon (C2+ ) products is attractive but with poor selectivity and activity due to the low-efficient CC coupling. Herein, a lithium vacancy-tuned Li2 CuO2 with square-planar [CuO4 ] layers is developed via an electrochemical delithiation strategy. Density functional theory calculations reveal that the lithium vacancies (VLi ) lead to a shorter distance between adjacent [CuO4 ] layers and reduce the coordination number of Li+ around each Cu, featuring with a lower energy barrier for COCO coupling than pristine Li2 CuO2 without VLi . With the VLi percentage of ≈1.6%, the Li2- x CuO2 catalyst exhibits a high Faradaic efficiency of 90.6 ± 7.6% for C2+ at -0.85 V versus reversible hydrogen electrode without iR correction, and an outstanding partial current density of -706 ± 32 mA cm-2 . This work suggests an attractive approach to create controllable alkali metal vacancy-tuned Cu catalytic sites toward C2+ products in electrochemical CO2 reduction.

Lithiation-Enabled High-Density Nitrogen Vacancies Electrocatalyze CO2 to C2 Products.

Electrochemical CO2 reduction to produce valuable C2 products is attractive but still suffers with relatively poor selectivity and stability at high current densities, mainly due to the low efficiency in the coupling of two *CO intermediates. Herein, it is demonstrated that high-density nitrogen vacancies formed on cubic copper nitrite (Cu3 Nx ) feature as efficient electrocatalytic centers for CO-CO coupling to form the key OCCO* intermediate toward C2 products. Cu3 Nx with different nitrogen densities are fabricated by an electrochemical lithium tuning strategy, and density functional theory calculations indicate that the adsorption energies of CO* and the energy barriers of forming key C2 intermediates are strongly correlated with nitrogen vacancy density. The Cu3 Nx catalyst with abundant nitrogen vacancies presents one of the highest Faradaic efficiencies toward C2 products of 81.7 ± 2.3% at -1.15 V versus reversible hydrogen electrode (without ohmic correction), corresponding to the partial current density for C2 production as -307 ± 9 mA cm-2 . An outstanding electrochemical stability is also demonstrated at high current densities, substantially exceeding CuOx catalysts with oxygen vacancies. The work suggests an attractive approach to create stable anion vacancies as catalytic centers toward multicarbon products in electrochemical CO2 reduction.