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The zein degradation was confirmed by the disappearance of the protein band in the electrophoresis gel, by the formation of the lower molecular weight fragments and also by the greater release of FTIC after enzymes incubation. In this context, the synthesis of responsive nanoparticles has great potential for application in pest management, increasing the selectivity and specificity of the system and contributing to a more sustainable agriculture.Mercury (Hg) is one of the most hazardous pollutants, widely distributed in water, atmosphere, and soil, while the Hg contents from different sources are greatly different. Until now, numerous reported methods are only suitable for a kind of sample because they cannot reconcile sensitivity and linear range. In this work, a tail-extensible DNA fluorescent probe for "turn on" detection of Hg2+ with tunable dynamic range and high sensitivity was developed, which was based on segmental hybridization between silver nanoclusters (AgNCs)-covered DNA and different guanine-rich DNAs. By adding adenine-guanine-cytosine (AGC) base repeats as a tail of the guanine-rich DNA, the formation constant of T-Hg2+-T complex was effectively modulated within two orders of magnitude. Based on it, a tunable dynamic range from 0.035 to 0.2 pM to 8.0-120.0 pM was achieved by combining four fluorescent probes with different tail lengths. The Hg2+contents from different sources were successfully measured. This evidenced the proposed sensor's application toward wide-field detection, which is useful for the direct and objective comparison of results from different sources, and therefore providing a way for solving the shortcomings of reported methods for Hg2+ detection. Additionally,this present method is simple, cost-effective and time-saving, ultrasensitive and highly selective, which is favorable for expanding its applications and subsequent mercury pollution control.Metabolomic responses of earthworms to neonicotinoids are important for understanding their molecular-level toxicity and assessing their ecological risks, but little is known until now. We investigated impact of imidacloprid (IMI, 52.6 ng/g) and dinotefuran (DIN, 52.5 ng/g) on Eisenia fetida metabolomics under single- and dual-compound exposure scenarios for one to four weeks. Dissimilar metabolites and anti-stress strategies were found for different neonicotinoids and exposure scenarios. Specifically, IMI exposure first increased myo-inositol and UDP-glucuronate associated with transmembrane absorption and transformation to IMI-urea, and then increased glutathione and fourteen amino acids (TCA cycle precursors) to resist stress and replenish energy. HSP990 clinical trial In contrast, worms exposed to DIN first prepared TCA cycle intermediates from glucosamine-6-phosphate and amino acids, suppressed urea cycle and DIN transformation, and then alleviated oxidative stress by increasing carnosine, nicotinate-D-ribonucleotide and nicotinamide-β-riboside. Dual exposure increased four eicosanoids by 1.6-1.9-fold, possibly associated with membrane lipid peroxidation; the amino acids consumed to balance the energy metabolism exhibited a wave-like pattern. This study first systematically revealed the compound/time/exposure scenario- dependent effects of trace neonicotinoids on earthworm metabolomics and advanced the understanding of their action modes. Neonicotinoid transformation was closely related to worms' metabolic profiles, providing important insights in contaminant fate in soil ecosystems.Microplastics (MPs) in marine and terrestrial environments have been intensively studied, but the dynamics of airborne MPs remains limited. Existing studies on atmospheric MPs are mostly derived from collection of atmospheric deposition, whereas direct measurements of airborne MPs are scarce. However, the abundance of airborne MPs is more relevant for evaluating human inhalation exposure risk. Herein, airborne MPs in indoor and outdoor environments from urban and rural areas of a coastal city in eastern China were investigated. MP concentrations (mean±SD) in indoor air (1583 ± 1180 n/m3) were an order of magnitude higher than outdoor air (189 ± 85 n/m3), and airborne MP concentrations in urban areas (224 ± 70 n/m3) were higher than rural areas (101 ± 47 n/m3). MPs smaller than 100 µm dominated airborne MPs, and the predominant shape of airborne MPs was fragments, as opposed to fibers. The larger MP size fractions contained a higher proportion of fibers, whereas the smaller size fractions were nearly exclusively composed of fragments. The health risk caused by ubiquitous airborne MPs should not be discounted as the maximum annual outdoor exposure of airborne MPs can reach 1 million/year, while indoor exposure may be even higher due to higher indoor airborne MP concentrations.Microplastics (MPs) have been widely detected in the environments, yet the sources of MPs in freshwater of remote areas at high altitude were not well understood. This study investigated the abundance and distribution of MPs in water bodies and sediments at the Qinghai-Tibet Plateau (QTP). MPs were detected in all samples (47 water and 33 sediment samples) with the mean abundance of 624.70 ± 411.39 items/m3 in water and 41.52 ± 22.31 items/kg in sediment. In descending order, the highest MP oncentrations were found in turbid rivers>agricultural channel water>lakes>ordinary rivers. The results showed that MP abundance was associated with the water quality (especially COD) on the QTP, and it was negatively correlated with altitude due to less human activities (especially agricultural activities) at high altitude areas. In addition, more abundant MPs with small sized was found in the higher altitudes than low ones. Determining the effects of different environments on the distribution and degradation of MPs in the high altitude area of the QTP, this study emphasized the attention to be given to this emerging pollutant in the high altitude remote areas.This paper reports the synthesis, characterization and detailed adsorption studies of rGO-MoS2 heterostructure. The heterostructure was explored for the adsorption of ofloxacin from the aqueous phase. Detailed studies were conducted to study the effect of crucial parameters such as pH of drug solution, adsorbent dose, temperature and initial drug concentration on the adsorption capacity. Even with a low surface area of 17.17 m2/g, the adsorbent exhibited maximum removal efficiency of 95% at a dose of 0.35 g/L and an initial drug concentration of 10 mg/L in 240 min. Thermodynamic study revealed the values for ∆H0 and ∆G0 to be - 101.15 and - 7.47 kJ/mol respectively, indicating that the process is spontaneous and exothermic in nature. The heterostructure adsorbent exhibited remarkable reusability and stability up to five cycles. The heterostructure combines excellent adsorption capabilities arising from the two-dimensional structures of rGO and MoS2 with the stronger and more specific interaction with the drug molecules which results in better performance towards the removal of the drug. The excellent performance of the heterostructure indicates that combining 2D materials can be a good strategy for producing highly efficient materials towards the adsorptive removal of pollutants.MXenes are a unique family of two-dimensional (2D) transition metal carbides and/or nitrides, which have been proven useful for energy storage, water purification, and biomedical applications. Herein, a kind of heterojunction structure was designed by grafting highly conductive MXene (Ti3C2) on the graphene oxide (GO) nanosheets, which was confirmed by Fourier transform infrared (FT-IR) spectroscopy, X-ray photoelectronic spectroscopy (XPS) and Raman results. Open circuit potential (OCP), electrochemical impedance spectroscopy (EIS) and salt spray measurements corroborated that inclusion of 0.5 wt% Ti3C2 or GO-Ti3C2 into epoxy zinc-rich coating (ZRC) effectively enhance the cathodic protection capability. Additionally, superior corrosion resistance was achieved by incorporation of GO-Ti3C2 into ZRC since GO-Ti3C2 in the coating improved the utilization rate of zinc particles and GO provided barrier protection for inhibiting the diffusion of corrosive agents. At the end of immersion, Rc value of ZRC/GO-Ti3C2 coating was 3.047 × 104 Ω·cm2, which was one order of magnitude higher than that of ZRC coating. Scanning electron microscope (SEM) and energy dispersive spectroscopy (EDS) measurements demonstrated that ZRC/GO-Ti3C2 coating exhibited lower speed of zinc particles oxidation and intact steel substrate. Hence, ZRC/GO-Ti3C2 coating exhibited the optimal corrosion resistance among the four kinds of coatings.A 35-day microcosmic experiment was conducted with lettuce (Lactuca sativa L.) and two metalaxyl (MET) enantiomers (R-MET and S-MET) to understand the roles of biochar in the enantioselective fate of chiral pesticides in soil-plant ecosystems. Wood waste-derived biochar (WBC) amendment effectively decreased the shoot concentrations of R-MET/S-MET and their metabolites R-MET/S-MET acid by 57.7-86.3% and 13.3-32.5%, respectively. The reduced uptake was mainly attributed to the decreased bioavailability of R-MET and S-MET. A lower fraction of R-MET was accumulated by the lettuce in the WBC-amended soils relative to the control, suggesting a decrease in the enantioselective uptake of the chiral pesticide MET in the presence of biochar. Regardless of the WBC amendment, no enantiomerization of MET or MET acid occurred. The application of WBC stimulated soil bacterial diversity, shifted the bacterial community, and enhanced the abundance of pesticide degrading bacteria (e.g., Luteimonas, Methylophilus, and Hydrogenophaga), which were responsible for the enantioselective degradation of MET in the soil. This work expands our understanding of the enantioselective fate of chiral pesticides in the biochar-amended soil ecosystems. These findings can be used to develop biochar-based technologies to remediate soils contaminated with these chiral pesticides to ensure food safety.Microbial biofilm has been found to impact the mobility of nanoparticles in saturated porous media by altering physicochemical properties of collector surface. However, little is known about the influence of biofilm's biological activity on nanoparticle transport and retention. Here, the transport of ferrihydrite nanoparticles (FhNPs) was studied in quartz sands coated with biofilm of Shewanella oneidensis MR-1 that is capable of reducing Fe(III) through extracellular electron transfer (EET). It was found that MR-1 biofilm coating enhanced FhNPs' deposition under different pH/ionic strength conditions and humic acid concentrations. More importantly, when the influent electron donor (glucose) concentration was increased to promote biofilm's EET activity, the breakthrough of FhNPs in biofilm-coated sands was inhibited. A lack of continuous and stable supply of electron donor, on the contrary, led to remobilization and release of the originally retained FhNPs. Column experiments with biofilm of EET-deficient MR-1 mutants (ΔomcA/ΔmtrC and ΔcymA) further indicated that the impairment of EET activity decreased the retention of FhNPs. It is proposed that the effective surface binding and adhesion of FhNPs that is required by direct EET cannot be neglected when evaluating the transport of FhNPs in sands coated with electroactive biofilm.

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