Henningsenlambertsen0412

Following such an accelerated mutagenesis-followed by selection approach, three phenotypes were successfully evolved resistance to antibiotics streptomycin and rifampicin (either individually or combined) and reversion of a synthetic uracil auxotrophy. Thus, these mutator devices could be applied to accelerate the evolution of metabolic pathways in long-term evolutionary experiments, alternating cycles of (inducible) mutagenesis coupled to selection schemes toward the desired phenotype(s).To date, few studies have examined the role of sea spray aerosols (SSAs) in human exposure to harmful and beneficial marine compounds. Two groups of phycotoxins (brevetoxins and ovatoxins) have been reported to induce respiratory syndromes during harmful algal blooms. The aerosolization and coastal air concentrations of other common marine phycotoxins have, however, never been examined. This study provides the first (experimental) evidence and characterization of the aerosolization of okadaic acid (OA), homoyessotoxin, and dinophysistoxin-1 using seawater spiked with toxic algae combined with the realistic SSA production in a marine aerosol reference tank (MART). The potential for aerosolization of these phycotoxins was highlighted by their 78- to 1769-fold enrichment in SSAs relative to the subsurface water. To obtain and support these results, we first developed an analytical method for the determination of phycotoxin concentrations in SSAs, which showed good linearity (R2 > 0.99), recovery (85.3-101.8%), and precision (RSDs ≤ 17.2%). We also investigated natural phycotoxin air concentrations by means of in situ SSA sampling with concurrent aerosolization experiments using natural seawater in the MART. This approach allowed us to indirectly quantify the (harmless) magnitude of OA concentrations (0.6-51 pg m-3) in Belgium's coastal air. Overall, this study provides new insights into the enriched aerosolization of marine compounds and proposes a framework to assess their airborne exposure and effects on human health.ConspectusMetal-organic frameworks (MOFs) are a huge, rapidly growing class of crystalline, porous materials that consist of inorganic nodes linked by organic struts. Offering the advantages of thermal stability combined with high densities of accessible reactive sites, some MOFs are good candidate materials for applications in catalysis and separations. Such MOFs include those with nodes that are metal oxide clusters (e.g., Zr6O8, Hf6O8, and Zr12O22) and long rods (e.g., [Al(OH)]n). These nanostructured metal oxides are often compared with bulk metal oxides, but they are in essence different because their structures are not the same and because the MOFs have a high degree of uniformity, offering the prospect of a deep understanding of reactivity that is barely attainable for most bulk metal oxides because of their surface heterogeneity. This prospect is being realized as it has become evident that adventitious components on MOF node surfaces, besides the linkers, are crucial. These ligands arise from modulatve sites themselves (e.g., terminal OH groups in tert-butyl alcohol (TBA) dehydration). selleck inhibitor Surprisingly, in view of the catalytic importance of such ligands on bulk metal oxides, their subtle chemistry on MOF nodes is only recently being determined. We describe (1) methods for identifying and quantifying node ligands (especially by IR spectroscopy and by 1H NMR spectroscopy of MOFs digested in NaOH/D2O solutions); (2) node ligand surface chemistry expressed as reaction networks; (3) catalysis, with mechanisms and energetics determined by density functional theory (DFT) and spectroscopy; and (4) MOF unzipping by reactions of linker carboxylate ligands with reactants such as alcohols that break node-linker bonds, a cause of catalyst deactivation and also an indicator of node-linker bond strength and MOF stability.Actin is the most abundant protein in eukaryotic cells and is key to many cellular functions. The filamentous form of actin (F-actin) can be studied with help of natural products that specifically recognize it, as for example fluorophore-labeled probes of the bicyclic peptide phalloidin, but no synthetic probes exist for the monomeric form of actin (G-actin). Herein, we have panned a phage display library consisting of more than 10 billion bicyclic peptides against G-actin and isolated binders with low nanomolar affinity and greater than 1000-fold selectivity over F-actin. Sequence analysis revealed a strong similarity to a region of thymosin-β4, a protein that weakly binds G-actin, and competition binding experiments confirmed a common binding region at the cleft between actin subdomains 1 and 3. Together with F-actin-specific peptides that we also isolated, we evaluated the G-actin peptides as probes in pull-down, imaging, and competition binding experiments. While the F-actin peptides were applied successfully for capturing actin in cell lysates and for imaging, the G-actin peptides did not bind in the cellular context, most likely due to competition with thymosin-β4 or related endogenous proteins for the same binding site.MXene is a generic name for a large family of two-dimensional transition metal carbides or nitrides, which show great promise in the field of transparent supercapacitors. However, the manufacturing of supercapacitor electrodes with a high charge storage capacity and desirable transmittance is a challenging task. Herein, a low-cost, large-scale, and rapid preparation of flexible and transparent MXene films via inkjet printing is reported. The MXene films realized the sheet resistance (Rs) of 1.66 ± 0.16 MΩ sq-1 to 1.47 ± 0.1 kΩ sq-1 at the transmissivity of 87-24% (λ = 550 nm), respectively, corresponding to the figure of merit (the ratio of electronic to optical conductivity, σDC/σOP) of ∼0.0012 to 0.13. Furthermore, the potential of inkjet-printed transparent MXene films in transparent supercapacitors was assessed by electrochemical characterization. The MXene film, with a transmittance of 24%, exhibited a superior areal capacitance of 887.5 μF cm-2 and retained 85% of the initial capacitance after 10,000 charge/discharge cycles at the scan rate of 10 mV s-1.