Multiferroicity in an organic charge-transfer salt that is suggestive of electric-dipole-driven magnetism

Multiferroics, showing simultaneous ordering of electrical and magnetic degrees of freedom, are remarkable materials as seen from both the academic and technological points of view. A prominent mechanism of multiferroicity is the spin-driven ferroelectricity, often found in frustrated antiferromagnets with helical spin order. There, as for conventional ferroelectrics, the electrical dipoles arise from an off-centre displacement of ions. However, recently a different mechanism, namely purely electronic ferroelectricity, where charge order breaks inversion symmetry, has attracted considerable interest. Here we provide evidence for ferroelectricity, accompanied by antiferromagnetic spin order, in a two-dimensional organic charge-transfer salt, thus representing a new class of multiferroics. We propose a charge-order-driven mechanism leading to electronic ferroelectricity in this material. Quite unexpectedly for electronic ferroelectrics, dipolar and spin order arise nearly simultaneously. This can be ascribed to the loss of spin frustration induced by the ferroelectric ordering. Hence, here the spin order is driven by the ferroelectricity, in marked contrast to the spin-driven ferroelectricity in helical magnets.     

Electrode structure analysis and surface characterization for lithium-ion cells simulated low-Earth-orbit satellite operation: II: Electrode surface characterization

As a sequence work to investigate the performance-degradation mechanism of an aged commercial laminated lithium-ion cell experiencing 4350-cycle charge–discharge in a simulated low-Earth-orbit (LEO) satellite operation, we performed the surface characterization of LiCoO₂ cathode and graphite anode by Fourier transform infrared-Attenuated total reflection (FTIR-ATR) and X-ray photoelectron spectroscopy (XPS) analysis in this work. Overall, the graphite anode had a larger change in surface chemistry than that of the LiCoO₂ cathode. Except the common surface components, we detected Co metal at the aged graphite surface in the first time. This Co metal deposition was believed to originate from Co²⁺ dissolution from LiCoO₂ cathode during prolonged cycling, and detrimental to structure stability of LiCoO₂ cathode which was a main cause of cell capacity loss. The amount of surface-film component was also estimated by FTIR analysis. Though the total amount of surface film increased, the organic (inorganic) surface film decreased (increased) with prolonged cycling.     

Identification of Anti-Severe Acute Respiratory Syndrome-Related Coronavirus 2 (SARS-CoV-2) Oxysterol Derivatives In Vitro

The development of effective antiviral drugs targeting the severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2) is urgently needed to combat the coronavirus disease 2019 (COVID-19). We have previously studied the use of semi-synthetic derivatives of oxysterols, oxidized derivatives of cholesterol as drug candidates for the inhibition of cancer, fibrosis, and bone regeneration. In this study, we screened a panel of naturally occurring and semi-synthetic oxysterols for anti-SARS-CoV-2 activity using a cell culture infection assay. We show that the natural oxysterols, 7-ketocholesterol, 22(R)-hydroxycholesterol, 24(S)-hydroxycholesterol, and 27-hydroxycholesterol, substantially inhibited SARS-CoV-2 propagation in cultured cells. Among semi-synthetic oxysterols, Oxy210 and Oxy232 displayed more robust anti-SARS-CoV-2 activities, reducing viral replication more than 90% at 10 μM and 99% at 15 μM, respectively. When orally administered in mice, peak plasma concentrations of Oxy210 fell into a therapeutically relevant range (19 μM), based on the dose-dependent curve for antiviral activity in our cell-based assay. Mechanistic studies suggest that Oxy210 reduced replication of SARS-CoV-2 by disrupting the formation of double-membrane vesicles (DMVs); intracellular membrane compartments associated with viral replication. Our study warrants further evaluation of Oxy210 and Oxy232 as a safe and reliable oral medication, which could help protect vulnerable populations with increased risk of developing COVID-19.     

17 beta-estradiol degradation by TiO2 photocatalysis as a means of reducing estrogenic activity

The degradation of 17 beta-estradiol (E2) in water by TiO2 photocatalysis was investigated; concurrently the estrogenic activity of the treated water was evaluated during the photocatalytic reactions by an estrogen screening assay. As a result, 10(-6) M of E2 was totally mineralized to CO2 in 1.0 g L-1 TiO2 suspension under UV irradiation for 3 h. 10 epsilon-17 beta-Dihydroxy-1,4-estradien-3-one and testosterone-like species were elucidated as intermediate products by GC/MS analysis. The mechanisms of E2 degradation by TiO2 photocatalysis were discussed not only experimentally but also theoretically by calculating the frontier electron densities of the E2 molecule. On the basis of the results obtained, it was concluded that the phenol moiety of the E2 molecule, one of the essential functional groups to interact with the estrogen receptor, should be the starting point of the photocatalytic oxidation of E2. This means that the estrogenic activity should be almost lost concurrently with the initiation of the photocatalytic degradation. Actually, the estrogenic activities of the intermediate products were negligible. TiO2 photocatalysis could be applied to water treatment to effectively remove natural and synthetic estrogens without producing biologically active intermediary products.     

Identification and characterization of genes involved in glutathione production in yeast

Glutathione is a major peptide protecting cells against oxidative stress. To study the cellular processes affecting intracellular glutathione production, we screened Saccharomyces cerevisiae mutant collections and identified new eight yeast deletion mutants that produced more than 1.2-fold higher levels of intracellular glutathione: chc1, cst6, ddc1, def1, pep12, rts1, ubp6, and yih1. Furthermore, overexpression of the DEF1 and CYS4 genes led to a higher production of glutathione, similar to overexpression of GSH1. A multiplier effect on activation of glutathione synthesis was observed by a combination of overexpression of GSH1 and deletion of one of the eight genes. Metabolome analysis of the def1, pep12, and ubp6 deletion mutant, and DEF1-overexpressing strains showed that levels of intracellular methionine and oxidized glutathione were higher than in the control strains, suggesting that methionine biosynthesis was activated and the oxidative stress response was increased in these glutathione-overproductive strains. Moreover, overexpression of GSH1, CYS4, and DEF1 also increased glutathione production in Candida utilis. Taken together, these results will significantly contribute to more effective industrial production of glutathione using yeasts.     

Comparative study on delivery of phosphatidic acid to serum-free culture of Chinese hamster ovary cells

Liposomes containing phosphatidic acid (PA) and inclusion complexes of PA with methyl-beta-cyclodextrin (CD) were compared with PA dispersion prepared with a nonionic surfactant, Tween 80, for their effect on the growth of Chinese hamster ovary (CHO) cells in serum-free culture. All of the types of PA preparation were capable of promoting cell growth to almost the same high extent, indicating that the efficacy of PA in stimulating cellular growth may not depend on the preparation method.     

Introduction of Localized Spins to Strongly Correlated One-Dimensional Electronic System at Quarter-Filling

We discuss an interesting interplay of charge and spin degrees of freedom under the combination of the localized spins and the quarter-filled one-dimensional electronic system. The electronic system has on-site and intersite Coulomb interactions, U and V, respectively, which cooperate with the Kondo coupling, J, leading to a rich phase diagram with charge ordering and the ferromagnetism. The origin of the ferromagnetism is being discussed in comparison with the double exchange mechanism.