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5-electron transfer based on low- and high-spins FeII/FeIII couples, which is verified by ex situ XRD, XPS, and DFT calculations. The K-ion full battery is also demonstrated using a graphite anode with a high energy density of 282.7 Wh·kg-1. This work may promote more studies on PBA electrodes and accelerate the development of KIBs.Many microorganisms possess the capacity for producing multiple antibiotic secondary metabolites. In a few notable cases, combinations of secondary metabolites produced by the same organism are used in important combination therapies for treatment of drug-resistant bacterial infections. However, examples of conjoined roles of bioactive metabolites produced by the same organism remain uncommon. During our genetic functional analysis of oxidase-encoding genes in the everninomicin producer Micromonospora carbonacea var. aurantiaca, we discovered previously uncharacterized antibiotics everninomicin N and O, comprised of an everninomicin fragment conjugated to the macrolide rosamicin via a rare nitrone moiety. These metabolites were determined to be hydrolysis products of everninomicin P, a nitrone-linked conjugate likely the result of nonenzymatic condensation of the rosamicin aldehyde and the octasaccharide everninomicin F, possessing a hydroxylamino sugar moiety. Rosamicin binds the erythromycin macrolide binding site approximately 60 Å from the orthosomycin binding site of everninomicins. Ataluren However, while individual ribosomal binding sites for each functional half of everninomicin P are too distant for bidentate binding, ligand displacement studies demonstrated that everninomicin P competes with rosamicin for ribosomal binding. Chemical protection studies and structural analysis of everninomicin P revealed that everninomicin P occupies both the macrolide- and orthosomycin-binding sites on the 70S ribosome. Moreover, resistance mutations within each binding site were overcome by the inhibition of the opposite functional antibiotic moiety binding site. These data together demonstrate a strategy for coupling orthogonal antibiotic pharmacophores, a surprising tolerance for substantial covalent modification of each antibiotic, and a potential beneficial strategy to combat antibiotic resistance.ConspectusAs the world transitions away from fossil fuels, energy storage, especially rechargeable batteries, could have a big role to play. Though rechargeable batteries have dramatically changed the energy landscape, their performance metrics still need to be further enhanced to keep pace with the changing consumer preferences along with the increasing demands from the market. For the most part, advances in battery technology rely on the continuing development of materials science, where the development of high-performance electrode materials helps to expand the world of battery innovation by pushing the limits of performance of existing batteries. This is where vanadium-based compounds (V-compounds) with intriguing properties can fit in to fill the gap of the current battery technologies.The history of experimenting with V-compounds (i.e., vanadium oxides, vanadates, vanadium-based NASICON) in various battery systems, ranging from monovalent-ion to multivalent-ion batteries, stretches back decades. They artheir working state. The mechanistic insights covered in this Account could be used as a fundamental guidance for several key strategies in electrode materials design in terms of dimension, morphology, composition, and architecture that govern the rate and degree of chemical reaction.This is the first report on the enhanced thermoelectric (TE) properties of novel reaction-temperature (TRe) and duration-induced Bi2S3-Bi nanocomposites synthesized using a facile one-step polyol method. They are well characterized as nanorod composites of orthorhombic Bi2S3 and rhombohedral Bi phases in which the latter coats the former forming Bi2S3-Bi core-shell-like structures along with independent Bi nanoparticles. A very significant observation is the systematic reduction in electrical resistivity ρ with a whopping 7 orders of magnitude (∼107) with just reaction temperature and duration increase, revealing a promising approach for the reduction of ρ of this highly resistive chalcogenide and hence resolving the earlier obstacles for its thermoelectric application potentials in the past few decades. Most astonishingly, a TE power factor at 300 K of the highest Bi content nanocomposite pellet, made at 27 °C using ∼900 MPa pressure, is 3 orders of magnitude greater than that of hot-pressed Bi2S3. Its highest ZT at 325 K of 0.006 is over twice of that of similarly prepared CuS or Ag2S-based nanocomposites. A significantly improved TE performance potential near 300 K is demonstrated for these toxic-free and rare-earth element-free TE nanocomposites, making the present synthesis method as a pioneering approach for developing enhanced thermoelectric properties of Bi2S3-based materials without extra sintering steps.Lung injury with COVID-19 may be due to a complex underlying pathophysiology. Cytokine release syndrome appears to be a catalyst of different inflammatory pathways promoting lung parenchymal injury and thromboembolic phenomena ("dual hit" injury). Recently, severe neurological manifestations such as acute disseminated encephalomyelitis, which may be not linked to lung pathology, have been identified in COVID-19, contributing thus further to the versatility of its clinical features.Electrocatalytic water splitting in acidic media based on a proton-exchange membrane (PEM) is a promising technique for the large-scale production of hydrogen. However, developing electrocatalysts with high activity and excellent stability for an oxygen evolution reaction (OER) in acidic media is still a big challenge. Herein, a Ce x -IrO2 catalyst supported on N-doped porous carbon (NPC) was developed via doping Ce into IrO2 nanoparticles. The Ce x -IrO2 nanoparticles were uniformly distributed on NPC due to the high surface area. The optimized Ce0.2-IrO2@NPC delivers a low overpotential of 224 mV and excellent stability of 100 h in 0.5 M H2SO4 at 10 mA cm-2. Density functional theory (DFT) calculations indicated that the introduction of Ce could modify the electronic structure of IrO2, decreasing the energy barrier of the rate-determining step for OER and enhancing the electrochemical OER performance. Our work opens up a new way of developing anodic electrocatalysts, which can be stably applied in acidic media.