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ons are facilitated, such as droplet transfer, microreactor and other potential fields.The pristine g-C3N4 (BCN) with a low conversion efficiency of CO2 exits with small specific surface area, weak CO2 adsorption and severe recombination of photo-generated charges. The stripping of few-layer g-C3N4 represents excellent photocatalytic performance, which attracts extensive attention in photocatalytic CO2 reduction. In the present study, the ultra-thin porous g-C3N4 (THCN) with high specific surface area and high position of conduction band was prepared using step-by-step synergistic exfoliation. Further, we treated it with HCl-assisted hydrothermal stripping and successive thermal stripping/etching in air. Our results showed that the THCN exhibited the best CO2 conversion efficiency from CO2 to CH4 and CO fuels, compared with g-C3N4 (HCN) prepared by HCl-assisted hydrothermal stripping and g-C3N4 (TCN) prepared by thermal stripping/etching in air. Further, the excellent photocatalytic performance for CO2 reduction was mainly attributed to its high specific surface area and rich pores, excellent separation and utilization efficiency of photo-generated carriers, and upper position of conduction band. Due to its wide band gap and high specific surface area, the THCN also showed significantly better degradation for Rhodamine B than BCN, HCN and TCN. Nonetheless, using a simple two-step stripping strategy, we prepared and obtained an ultra-thin porous g-C3N4 nanosheets with a high specific surface area for CO2 conversion to CH4 and CO fuels. This ultimately provided a reference for preparation of other two-dimensional ultra-thin materials for CO2 reduction.This article investigates the main aspects of the surface chemistry properties of the lactate oxidase (LacOx) enzyme monolayer at the air-subphase interface. Surface chemistry study determined the important properties like the surface packing and stability of the formed layer, whereas the spectroscopic experiments provided information regarding its secondary structure conformation of the enzyme. We have demonstrated that the LacOx in the monolayer form remained active for extended time period. In accordance to the data obtained from the isotherm it was also found that LacOx forms a stable monolayer that does not aggregate at the air-subphase interface. The stability of the monolayer at the air-subphase interface was studied by using compression-decompression cycles which revealed the stability with no significant evidence of aggregates or irreversible domains. This was further confirmed by UV-vis absorption and fluorescence measurements. Spectra from circular dichroism (CD) showed that the LB film retains the characteristic of an α-helix conformation.

Characterization of contact angle hysteresis on soft surfaces is sensitive to the measurement protocol and might present adventitious time-dependencies. Selleck AZD4547 Contact line dynamics on solid surfaces is altered by the surface chemistry, surface roughness and/or surface elasticity. We observed a "slow" spontaneous relaxation of static water sessile drops placed on elastic surfaces. This unexpected drop motion reveals unresolved equilibrium configurations that may affect the observed values of contact angle hysteresis. Drop relaxation on deformable surfaces is partially governed by a viscoelastic dissipation located at the contact line.

In this work, we studied the natural relaxation of water drops formed on several smooth PDMS surfaces with different elastic moduli. We monitored in time the contact angle and contact radius of each drop. For varying the initial contact angle, we used the growing-shrinking drop method.

We postulate that the so-called "braking effect", produced by the surface deformability, affects the contact line velocity and in consequence, the contact angle measurements. We conclude that the wetting properties of elastic surfaces should be properly examined with reliable values of contact angle measured after drop relaxation.

We postulate that the so-called "braking effect", produced by the surface deformability, affects the contact line velocity and in consequence, the contact angle measurements. We conclude that the wetting properties of elastic surfaces should be properly examined with reliable values of contact angle measured after drop relaxation.Magnetic spin exchange-coupled magnets have been investigated for obtaining an enhanced energy product, however, approaches at the nanoscale have been greatly restricted because of the lack of consideration of the relationships among the individual components. Here, we suggest a facile strategy for fabricating exchange-coupled nanomagnets with a large energy product. As a bottom-up approach, this work introduces a combined thermal decomposition and reduction/diffusion process to obtain a magnetic spin exchange coupled SmCo5/Co nanocomposite magnet. The SmCo5/Co nanocomposite magnet was fabricated through a three-step approach (1) chemical synthesis of Co@SmOx nanoparticles and Co nanoparticles as hard and soft magnetic phases, respectively, (2) 3-dimensional alternating arrangement of both magnetic phases and (3) a reduction/diffusion process for the magnetic spin exchange interaction. Our results demonstrate that an effective magnetic spin exchange interaction strongly depends on the dimension and arrangement of the hard and soft phases, which were synthetically tuned to be within the magnetic domain wall size.Creating rich vacancies and designing distinct micro-morphology are considered as effective strategies for boosting the electrochemical performances of sodium ion battery (SIB) electrode materials. In this paper, a variety of MoS2 nanostructures with different sulfur vacancies concentration and morphologies are successfully constructed by a hydrothermal method combined with various-temperature calcination treatment in a Ar/H2 mixed atmosphere. Employed as a free-standing anode for SIBs, the flower-like MoS2-x microspheres assembled by the intertwined nanosheet arrays (MoS2-x-800) delivers highest specific capacity of 525.3 mAh g-1 and rate capability, as well as extraordinarily stable cycle life with almost no loss of capacity after 420 cycles. The favorable sodium storage properties are mainly ascribed to the cooperated effects of superior intrinsic conductivity and richer active sites generated by sulfur vacancies, and numerous interspace achieved by the intersection of neighbouring nanosheets. Meanwhile, through ex situ analyses, the reversible charge/discharge mechanism of the obtained MoS2-x-800 is revealed reasonably. This work not only brings new insights into the design of high-performance electrode materials for SIBs, but also makes a great step forward in the practical applications of transition metal sulfides in energy storage systems.

The underlying resistance mechanisms, defence systems, mobilome, virulome, clonality and global phylogenetic relationship of a novel sequence type (ST) 658 Aeromonas hydrophilia (A34a) isolated from a pig abattoir in South Africa was determined using whole-genome sequence (WGS) technology.

Following isolation on chromogenic agar (CHROMID® CARBA SMART), microbial identification and antibiotic susceptibility testing were performed using a VITEK®2 platform. Genotyping involved WGS performed with an Illumina MiSeq platform.

The antibiotic resistome agreed with the resistance phenotype of the isolate and included antibiotic resistance determinants for β-lactams (bla

and bla

). BLASTn analysis of resistome-encoding contigs affirmed chromosomally-mediated resistance. BURST algorithmic analysis identified the novel ST658 as a satellite variant. Virulome analysis predicted virulence genes of Aeromonas whose expression are critical for establishing infection in the host. Global phylogenomic analyses showed strain A34a is closely related to two international isolates from Sri Lanka (Ae25) and the USA (RU34A), although there is little to suggest that it was imported from abroad.

This is the first report on the genomic analysis of a novel ST658 A. hydrophilia, offering useful insights into its pathogenicity and global phylogenetics.

This is the first report on the genomic analysis of a novel ST658 A. hydrophilia, offering useful insights into its pathogenicity and global phylogenetics.Fusarium species cause many diseases in plants and humans, which results in a great number of economic losses every year. The management of plant diseases and related human diseases caused by Fusarium is challenging as many kinds of Fusarium may be intrinsically resistant to antifungal drugs, not to mention the fact that they can acquire drug resistance, which is common in clinical practice. To date, the drug resistance of Fusarium is mainly related to target alterations, drug efflux and biofilm formation. This article reviews recent studies related to the mechanism of Fusarium resistance, and summarizes the key molecules affecting resistance.

Carbapenem resistance has emerged inEscherichia coli, including sequence type 131 (ST131) and its fluoroquinolone-resistant H30R subclone, the leading cause of extraintestinal E. coli infections globally. Meropenem/vaborbactam (MVB) is a recently approved carbapenem/β-lactamase inhibitor combination with broad-spectrum inhibition of β-lactamases, including serine carbapenemases. The activity of MVB against carbapenem-resistant (CR) E. coli infections in relation to phylogenetic background, resistance genotype and geographical region is unknown.

We characterised 140 contemporary CR clinicalE. coli isolates from 17 non-US countries (2003-2017) for phylogroup, clonal group (including ST131, H30R and the CTX-M-15-associated H30Rx subset), relevant β-lactamase genes, and broth microdilution MICs for MVB and 11 comparators.

Overall, MVB was moderately active (66% susceptible), more so than all comparators except tigecycline and amikacin (100% and 74% susceptible, respectively). Most MVB-non-susceptible isolat phenotypes, although this likely will vary with the local prevalence of specific E. coli lineages and carbapenem resistance mechanisms.

The aim of this study was to investigate the biological characteristics and effect of antibiotic treatment for different Mycoplasma pneumoniae isolates co-infecting the same patient.

Two throat swab specimens from a single patient, on the day of admission (Sp01) and discharge (Sp13), were liquid cultured and subcultured on agar medium to obtain M. pneumoniae monoclones. The 23S rRNA gene of 50 monoclones from specimens Sp01 and Sp13 were analysed. Real-time PCR assay was used for detection of mutations and genotyping. Two typical monoclones were isolated for antimicrobial susceptibility testing.

Genotype 1 monoclones accounted for 70.8% (34/48) in Sp01 and 95.7% (44/46) in Sp13. All genotype 1 monoclones were of the 4-5-7-2 multilocus variable-number tandem-repeat analysis (MLVA) type, while all genotype 2 monoclones were 3-5-6-2 MLVA type. The genotype 1 monoclone, which harboured the A2063G mutation in 23S rRNA gene, was resistant to erythromycin and azithromycin in vitro, whilst genotype 2, which did not carry the mutation, was susceptible to macrolides. The proportion of macrolide-resistant M. pneumoniae monoclones in the specimen cultures collected rose from 70.8% to 95.7% at the time of discharge.

This is the first report on the isolation of macrolide-resistant and -susceptible strains of M. pneumoniae from the same patient. After treatment, the proportion of macrolide-resistant M. pneumoniae increased, but the patient still carried viable macrolide-susceptible strains, meaning that the macrolide-susceptible strains did not disappear completely.

This is the first report on the isolation of macrolide-resistant and -susceptible strains of M. pneumoniae from the same patient. After treatment, the proportion of macrolide-resistant M. pneumoniae increased, but the patient still carried viable macrolide-susceptible strains, meaning that the macrolide-susceptible strains did not disappear completely.