Biocatalytic enhancement of laccase immobilized on ZnFe_(2)O_(4) nanoparticles and its application for degradation of textile dyes

Efficient and convenient treatment of industrial dyeing wastewater is of great significance to guarantee human and animal health.This work presented the enhanced catalytic activity at pH 3.0 of laccase immobilized on amino-functionalized ZnFe_(2)O_(4) nanoparticles(ZnFe_(2)O_(4)-laccase)and its application for the degradation of textile dyes.Due to the existence of a large number of oxygen vacancies on the surface of the ZnFe_(2)O_(4) nanoparticles,negative ions accumulated on the magnetic carriers,which resulted in a harsh optimal pH value of the ZnFe_(2)O_(4)-laccase.Laccase activity assays revealed that the ZnFe_(2)O_(4)-laccase possessed superior pH and thermal stabilities,excellent reusability,and noticeable organic solvent tolerance.Meanwhile,the ZnFe_(2)O_(4) laccase presented efficient and sustainable degradation of high concentrations of textile dyes.The initial decoloration efficiencies of malachite green(MG),brilliant green(BG),azophloxine,crystal violet(CV),reactive blue 19(RB19),and procion red MX-5B were approximately 99.1%,95.0%,93.3%,87.4%,86.1%,and 85.3%,respectively.After 10 consecutive reuses,the degradation rates of the textile dyes still maintained about 98.2%,92.5%,83.2%,81.5%,79.8%and 65.9%,respectively.The excellent dye degradation properties indicate that the ZnFe_(2)O_(4)-laccase has a technical application in high concentrations of dyestuff treatment.

Layered kagome compound Na_(2)Ni_(3)S_(4)with topological flat band

We report structural and electronic properties of Na_(2)Ni_(3)S_(4),a quasi-two-dimensional compound composed of alternating layers of[Ni_(3)S_(4)]^(2-)and Na^(+).The compound features a remarkable Ni-based kagome lattice with a square planar configuration of four surrounding S atoms for each Ni atom.Magnetization and electrical measurements reveal a weak paramagnetic insulator with a gap of about 0.5 eV.Our band structure calculation highlights a set of topological flat bands of the kagome lattice derived from the rotated dxz-orbital with C_(3)+T symmetry in the presence of crystal-field splitting.

Constructing oxygen vacancy‐regulated cobalt molybdate nanoflakes for efficient oxygen evolution reaction catalysis

Oxygen evolution reaction(OER)is the dominant step for plenty of energy conversion and storage technologies.However,the OER suffers from sluggish kinetics and high overpotential due to its complex 4‐electron/proton transfer mechanism.Thus,developing efficient electrocatalysts is particularly urgent to accelerate OER catalysis but still remains a great challenge.Herein,we have synthesized the novel cobalt molybdate nanoflakes(CoMoO_(4)‐O_(v)‐n@GF)with adjustable oxygen vacancies contents by in situ constructing CoMoO_(4) nanoflakes on graphite felt(GF)and annealing treatment under the reduction atmosphere.The best‐performing CoMoO_(4)‐O_(v)‐2@GF with optimal oxygen vacancies content shows splendid electrocatalytic performance with the low overpotential(296 mV at 10 mA cm^(‒2))and also small Tafel slope(62.4 mV dec^(‒1))in alkaline solution,which are comparable to those of the RuO_(2)@GF.The experimental and the density functional theory calculations results reveal that the construction of optimal oxygen vacancies in CoMoO_(4) can expose more active sites,narrow the band‐gap to increase the electrical conductivity,and modulate the free energy of the OER‐related intermediates to accelerate OER kinetics,thus improving its intrinsic activity.

一例患者经颈静脉肝内门体分流术术中碘克沙醇致过敏性休克后顺利完成手术及文献分析

河北医科大学第二医院消化内科收治一例68岁患者,局部麻醉下行经颈静脉肝内门体分流术(transjugular intrahepatic portosystem shunt,TIPS),使用碘克沙醇注射液高压造影,15分钟后患者出现血压下降、皮肤瘙痒等症状,考虑患者出现过敏性休克,立即给予抗过敏、抗休克等急救治疗措施。患者生命体征指标逐渐恢复,过敏性休克症状逐渐消失,手术继续且顺利完成,无并发症发生。现就此例经颈静脉肝内门体分流术术中碘克沙醇注射液致过敏性休克患者的抢救措施及治疗情况进行分析,旨在加强临床安全使用碘克沙醇的用药意识。当患者使用碘克沙醇注射液造影时,短时间内出现血压下降,皮肤瘙痒等问题时,可能发生了过敏性休克。术中应严密观察患者的病情,及时发现过敏症状并及时进行有效处理,是抢救过敏性休克的关键。

A Versatile Tetraphenylethene Derivative Bearing Excitation Wavelength Dependent Emission,Multistate Mechanochromism,Reversible Photochromism,and Circularly Polarized Luminescence and Its Applications in Multimodal Anticounterfeiting

Multimodal anticounterfeiting has become increasingly challenging in modern society to guarantee information security and the safety of property.In this study,a versatile cholesterol-containing tetraphenylethene derivative is shown to have multiple optical properties,including stimuli-responsive fluorescence,reversible photochromism,excitation wavelength dependent luminescence,and circularly polarized luminescence.After the application of diverse processing methods(writing,screen painting,drawing,and pyrography),we found that this molecule can serve as an anticounterfeiting toolbox to provide rich anticounterfeiting effects through the synergistical use of multiple optical properties.This work offers important insight for designing novel small organic molecules for advanced multimodal anticounterfeiting technology.

BRF1 ameliorates LPS-induced inflammation through autophagy crosstalking with MAPK/ ERK signaling

Inflammation is indispensable for host defense,whereas excessive inflammation often develop inflammatory diseases.Autophagy is thought to be engaged in many extracellular stress responses,such as starvation and innate immunity.Thus,autophagy plays an important role in maintaining homeostasis.The purpose of this study was to elucidate the function of BRF1 in the regulation of inflammation and autophagy response in macrophages.We found that BRF1 inhibited the LPS-induced inflammatory factors expression and the autophagy flux in macrophage.Furthermore,inhibition autophagy with 3-MA can attenuate the suppressive effect of BRF1 on LPS-mediated inflammation.In addition,MAPK/ERK signaling pathway was involved in the BRF1 inhibition inflammation and autophagy in macrophages.These findings indicate that BRF1 attenuates LPS-induced inflammatory factors secretion through autophagy,at least in part,through MAPK/ERK signaling pathway.

Network pharmacology-based strategy to investigate harmacological mechanisms of Isodon serra(Maxim.)Hara for treatment of inflammatory

Widely distributed in plants,ent-kaurane diterpenoids could reduce the incidence of inflammatory.The most important active ingredient of Isodon serra(Maxim.)Hara is ent-kaurane diterpenoids,which contribute to the anti-inflammatory pharmacological effects of Isodon serra.However,the ingredients,the active compounds,drug targets,inflammatory targets and exact molecular mechanism of Isodon serra in treating inflammatory are still unclear.The purpose of this study was to use the method of network pharmacological analysis to find the active compounds in Isodon serra.These active compounds match the library of ent-kaurane diterpenoids compounds we established,and we find all the eligible ent-kaurane diterpenoids compounds.Isodon serra related and anti-inflammatory targets were found and then combined to get intersection,which represented potential anti-inflammatory targets of active compounds in Isodon serra.Moreover,anti-inflammatory targets and active compounds targets protein-protein interaction network were merged to get the protein-protein interaction network intersection and core genes in anti-inflammatory target protein-protein interaction network.For the anti-inflammatory targets of Isodon serra,Gene Ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)pathway analysis were executed to confirm gene functions of Isodon serra in antagonizing inflammation.Finally,TCMSP analysis identified 10 active compounds out of 48 ent-kaurane.The pathway analysis showed enrichment for different pathways like AGE-RAGE signaling pathway in diabetic complications,small cell lung cancer and human cytomegalovirus infection,which were all connected to inflammatory.On the whole,the proposed method clearly identified the ent-kaurane diterpenoids of Isodon serra and the results gave the active compounds of Isodon serra for the first time.The combining use of the qualitative analysis of traditional Chinese medicine(TCM)and network pharmacological methods could discover potential drug targets and reveal the biological process of TCM,which would open up a new approach in the study of TCM in future.

Glassy magnetic ground state in layered compound MnSb_(2)Te_(4)

As a sister compound of MnBi_(2)Te_(4),the highquality MnSb_(2)Te_(4) single crystals are grown via solid-state reaction where prolonged annealing and narrow temperature window play critical roles on account of its thermal metastability.Single-crystal X-ray diffraction(SCXRD)analysis on MnSb_(2)Te_(4) illustrates a crystal model that is isostructural to MnBi_(2)Te_(4),consisting of Te-Sb-Te-Mn-Te-Sb-Te septuple layers(SLs)stacking in an ABC sequence.However,MnSb_(2)Te_(4) reveals a more pronounced cation intermixing in comparison with MnBi_(2)Te_(4),comprising 28.9(7)%Sb antisite defects on the Mn(3a)site and 19.3(6)%Mn antisite defects on the Sb(6c)site,which may give rise to novel magnetic properties in emerging layered MnBi_(2)Te_(4)-family materials.Unlike the antiferromagnetic(AFM)nature in MnBi_(2)Te_(4),MnSb_(2)Te_(4) exhibits a glassy magnetic ground state below 24 K and can be easily tuned to a ferromagnetic state under a weak applied magnetic field.Its magnetic hysteresis,anisotropy,and relaxation process are investigated in detail via static and dynamic magnetization measurements.Moreover,anomalous Hall effect as a p-type conductor is demonstrated with transport measurements.This work grants MnSb_(2)Te_(4) a possible access to the future exploration of exotic quantum physics by removing the odd/even layer number restraint in realizing quantum transport phenomena in intrinsic AFM MnBi_(2)Te_(4)-family materials,as a result of the crossover between its magnetism and potential topology arising from the Sb-Te layer.

Revealing the Role of d Orbitals of Transition-Metal-Doped Titanium Oxide on High-Efficient Oxygen Reduction

Precise catalysis is critical for the high-quality catalysis industry.However,it remains challenging to fundamentally understand precise catalysis at the atomic orbital level.Herein,we propose a new strategy to unravel the role of specific d orbitals in catalysis.The oxygen reduction reaction(ORR)catalyzed by atomically dispersed Pt/Co-doped Ti_(1−x)O_(2) nanosheets(Pt_(1)/Co_(1)-Ti_(1−x)O_(2))is used as a model catalysis.The z-axis d orbitals of Pt/Co-Ti realms dominate the O2 adsorption,thus triggering ORR.In light of orbital-resolved analysis,Pt_(1)/Co_(1)-Ti_(1−x)O_(2) is experimentally fabricated,and the excellent ORR catalytic performance is further demonstrated.Further analysis reveals that the superior ORR performance of Pt_(1)-Ti_(1−x)O_(2) to Co_(1)-Ti_(1−x)O_(2) is ascribed to stronger activation of Ti by Pt than Co via the d-d hybridization.Overall,this work provides a useful tool to understand the underlying catalytic mechanisms at the atomic orbital level and opens new opportunities for precise catalyst design.

Intra-host Ebola viral adaption during human infection

The onsite next generation sequencing(NGS)of Ebola virus(EBOV)genomes during the 2013–2016 Ebola epidemic in Western Africa provides an opportunity to trace the origin,transmission,and evolution of this virus.Herein,we have diagnosed a cohort of EBOV patients in Sierra Leone in 2015,during the late phase of the outbreak.The surviving EBOV patients had a recovery process characterized by decreasing viremia,fever,and biochemical parameters.EBOV genomes sequenced through the longitudinal blood samples of these patients showed dynamic intra-host substitutions of the virus during acute infection,including the previously described short stretches of 13 serial TNC mutations.Remarkably,within individual patients,samples collected during the early phase of infection possessed Ts at these nucleotide sites,whereas they were replaced by Cs in samples collected in the later phase,suggesting that these short stretches of TNC mutations could emerge independently.In addition,up to a total of 35 nucleotide sites spanning the EBOV genome were mutated coincidently.Our study showed the dynamic intra-host adaptation of EBOV during patient recovery and gave more insight into the complex EBOV-host interactions.