Precezomycin, a novel antibiotic biosynthetic precursor of cezomycin, from actinomycete Kitasatospora putterlickiae 10-13.

A novel antibiotic biosynthetic precursor of cezomycin, named precezomycin (1), was isolated from culture broth of actinomycete Kitasatospora putterlickiae 10-13. The planar structure was determined by 1D/2D NMR and HR(ESI)MS data analyses, and the absolute configurations were established by TDDFT calculation of ECD spectra. Precezomycin (1) exhibited moderate antibacterial activity against gram-positive bacteria including Staphylococcus aureus and Bacillus subtilis. The discovery of 1 extends the natural product family of cezomycin and provides a new insight into understanding the biosynthetic process of these polyether ionophore metabolites.

Stabilizing a non-IPR C2(13333)-C74 cage with Lu2C2/Lu2O: the importance of encaged non-metallic elements.

A difference in encaged non-metallic element (i.e., C2versus O) leads to a clear change of intramolecular interactions and shifts in redox potentials of Lu2C2@C2(13333)-C74 and Lu2O@C2(13333)-C74, as a result of their distinct molecular orbital energy levels. Different from these two endoherals whose HOMOs are located on the cage, experimentally absent Lu2@C2(13333)-C74 possesses a HOMO predominantly delocalized on the internal Lu-Lu bond, accompanied by a much smaller HOMO-LUMO gap, suggesting that the presence of a non-metallic unit broadens the electrochemical gaps and consequently improves the kinetic stability. These findings shed light on the role of non-metallic moieties in clusterfullerenes, providing valuable insights into the stability and properties of metallofullerenes.

Steering Lu3N clusters in C76-78 cages: cluster configuration dominated by cage transformation.

While the strong interaction between the internal unit and the fullerene cage inside metallofullerenes is widely acknowledged, how the cage transformation interacts with the cluster configuration remains elusive. For this purpose, we herein synthesized three metallofullerene molecules with an easy-to-compare cluster configuration and cage arrangement, namely Lu3N@Cs(17 490)-C76, Lu3N@C2(22 010)-C78, and Lu3N@D3h(5)-C78. The three lutetium-based nitride clusterfullerenes (NCFs) with small C76-78 carbon cages were synthesized by a modified arc-discharge method and their structures were unambiguously confirmed by X-ray crystallography. Notably, the cage transformation from Cs(17 490)-C76 to C2(22 010)-C78via a simple C2-unit insertion leads to a remarkable configuration change of the encapsulated Lu3N cluster from an unusual asymmetric plane to a common symmetric one. This close correlation between the cluster configuration and cage transformation is further confirmed by the pyramidal Lu3N cluster in Lu3N@D3h(5)-C78 other than the symmetric planar Lu3N unit in Lu3N@C2(22 010)-C78, as a result of an even larger difference in the cage arrangement. Astonishingly, such a cluster shrinkage, accompanied by an increase in the cage size from Cs(17 490)-C76 to D3h(5)-C78, is dramatically opposite to the cluster expansion with cage elongation found in La2C2- or Y2C2-based metallofullerenes.

Cluster-Geometry-Associated Metal-Metal Bonding in Trimetallic Carbide Clusterfullerenes.

Geometry configurations of the metallic clusters play a significant role in the involved bonding nature. Herein, we report the crystallographic characterization of unprecedented erbium-based trimetallic clusterfullerenes, namely, Er3C2@Ih(7)-C80, in which the inner Er3C2 cluster presents a lifted bat ray configuration with the C2 unit elevated by ∼1.62 Å above the Er3 plane. Within the plane, the Er···Er distances for Er1···Er2, Er1···Er2A, and Er2···Er2A are 3.4051(15), 3.4051(15), and 3.3178(15) Å, respectively, falling into the range of the metal-metal bonding. Density functional theory calculations unveil the three-center-one-electron Er-Er-Er bond in Er3C2@Ih(7)-C80 with one electron shared by three metals, and thus, its exceptional electronic structure can be expressed as (Er3)8+(C2)2-@C806-. Interestingly, with the further observation on the geometry configurations of the encapsulated clusters in M3C2@C2n (M = Sc, Y, and Lu) series, we find that the lifted bat ray configuration of the inner cluster is explicitly associated with the formation of the bonding interactions between the inner metals. This finding provides insights into the nature of metal-metal bonding and gives guidelines for the design of the single-molecule magnet.

EGCG Restricts PRRSV Proliferation by Disturbing Lipid Metabolism.

Porcine reproductive and respiratory syndrome virus (PRRSV) infection leads to late-term reproductive failure and respiratory illness that affect the global swine industry. Epigallocatechin gallate (EGCG) is a polyphenolic compound from green tea that exerts antiviral activity against diverse viruses. This study aimed to report an uncharacterized mechanism of how EGCG restricted PRRSV proliferation. EGCG showed no significant effects on cell viability, cell cycle progression, and apoptosis in porcine alveolar macrophages and MARC-145 cells. The treatment of cells with EGCG attenuated the replication of both highly pathogenic and less pathogenic PRRSV in vitro. The viral life cycle analysis demonstrated that EGCG affected PRRSV replication and assembly, but not viral attachment, entry, or release. Interestingly, EGCG treatment abrogated the increased lipid droplets formation and lipid content induced by PRRSV infection. We further demonstrated that EGCG blocked PRRSV-stimulated expression of the key enzymes in lipid synthesis. In addition, EGCG attenuated PRRSV-induced autophagy that is critical for PRRSV proliferation. The supplementation of oleic acid restored PRRSV replication and assembly under EGCG treatment. Together, our results support that EGCG inhibits PRRSV proliferation through disturbing lipid metabolism. IMPORTANCE Porcine reproductive and respiratory syndrome virus (PRRSV) is an enveloped single-positive-stranded RNA virus that causes acute respiratory distress in piglets and reproductive failure in sows, resulting in huge economic losses to the global swine industry. Several lines of evidence have suggested the crucial roles of lipids in PRRSV proliferation. Our previous report demonstrated that PRRSV activated lipophagy to facilitate viral replication through downregulating the expression of N-Myc downstream-regulated gene 1. The manipulation of lipid metabolism may be a new perspective to prevent PRRSV spread. In the present study, we reported that epigallocatechin-3-gallate (EGCG), the major component of green tea catechins, significantly attenuated PRRSV infection through inhibiting lipid synthesis and autophagy. Given that natural products derived from plants have helped in the prevention and treatment of various infectious diseases, EGCG has a great potential to serve as a safe and environmentally friendly natural compound to treat PRRSV infection.

Rubrene-Directed Structural Transformation of Fullerene (C60) Microsheets to Nanorod Arrays with Enhanced Photoelectrochemical Properties.

One-dimensional (1D) nanostructures possess huge potential in electronics and optoelectronics, but the axial alignment of such 1D structures is still a challenging task. Herein, we report a simple method that enables two-dimensional (2D) C60 microsheets to evolve into highly ordered nanorod arrays using rubrene as a structure-directing agent. The structural transformation is accomplished by adding droplets of rubrene-m-xylene solution onto C60 microsheets and allowing the m-xylene solvent to evaporate naturally. In sharp contrast, when rubrene is absent from m-xylene, randomly oriented C60 nanorods are produced. Spectroscopic and microscopic characterizations collectively indicate a rather plausible transformation mechanism that the close lattice match allows the epitaxial growth of rubrene on C60 microsheets, followed by the reassembly of dissolved C60 along the aligned rubrene due to the intermolecular charge-transfer (CT) interactions, leading to the formation of ordered nanorod arrays. Due to the aligned structures and the CT interactions between rubrene and C60, the photocurrent density of the nanorod arrays is improved by 31.2% in the UV region relative to the randomly oriented counterpart. This work presents a facile and effective strategy for the construction of ordered fullerene nanorod arrays, providing new ideas for the alignment of fullerene and other relevant organic microstructures.

Morphology Engineering of Fullerene[C70 ] Microcrystals: From Perfect Cubes, Defective Hoppers to Novel Cruciform-Pillars.

Controlled crystallization of fullerene molecules into ordered molecular assemblies is important for their applications. However, the morphology engineering of fullerene[C70 ] assemblies is challenging, and complicated architectures have rarely been reported due to the low molecular symmetry of C70 molecules, which makes their crystallization difficult to control and the low production yield as well. Herein, with the assistance of solvent intercalation, a general reprecipitation approach is reported to prepare morphologically controllable C70 microcrystals with mesitylene as a good solvent and n-propanol as a poor solvent in one solvent system without replacing specific solvents. A series of C70 microcrystals with high uniformity from perfect cubes and defective hoppers to novel cruciform-pillars are obtained by intentionally tuning C70 concentration and the volume ratio of mesitylene to n-propanol. Among them, novel cruciform-pillar-shaped microcrystals are obtained for the first time by further decreasing the amount of mesitylene in the solvent-intercalated microcrystals. Notably, the C70 concentration is a key parameter for the selective growth of C70 hopper, rather than the volume ratio of mesitylene to n-propanol. Interestingly, the hopper-shaped microcrystals exhibit excellent photoluminescence properties relative to those of cubes and cruciform-pillars owing to the enhanced light absorption, proving their potential applications in optoelectronic devices. This study offers new insights into the morphology-controlled synthesis of other micro/nanostructured organic microcrystals and the fine tuning of photoluminescence properties of organic crystals.

An effective inactivant based on singlet oxygen-mediated lipid oxidation implicates a new paradigm for broad-spectrum antivirals.

Emerging viral pathogens cause substantial morbidity and pose a severe threat to health worldwide. However, a universal antiviral strategy for producing safe and immunogenic inactivated vaccines is lacking. Here, we report an antiviral strategy using the novel singlet oxygen (1O2)-generating agent LJ002 to inactivate enveloped viruses and provide effective protection against viral infection. Our results demonstrated that LJ002 efficiently generated 1O2 in solution and living cells. Nevertheless, LJ002 exhibited no signs of acute toxicity in vitro or in vivo. The 1O2 produced by LJ002 oxidized lipids in the viral envelope and consequently destroyed the viral membrane structure, thus inhibiting the viral and cell membrane fusion necessary for infection. Moreover, the 1O2-based inactivated pseudorabies virus (PRV) vaccine had no effect on the content of the viral surface proteins. Immunization of mice with LJ002-inactiviated PRV vaccine harboring comparable antigen induced more neutralizing antibody responses and efficient protection against PRV infection than conventional formalin-inactivated vaccine. Additionally, LJ002 inactivated a broad spectrum of enveloped viruses. Together, our results may provide a new paradigm of using broad-spectrum, highly effective inactivants functioning through 1O2-mediated lipid oxidation for developing antivirals that target the viral membrane fusion process.

A CT reconstruction approach from sparse projection with adaptive-weighted diagonal total-variation in biomedical application.

For lack of directivity in Total Variation (TV) which only uses x-coordinate and y-coordinate gradient transform as its sparse representation approach during the iteration process, this paper brought in Adaptive-weighted Diagonal Total Variation (AwDTV) that uses the diagonal direction gradient to constraint reconstructed image and adds associated weights which are expressed as an exponential function and can be adaptively adjusted by the local image-intensity diagonal gradient for the purpose of preserving the edge details, then using the steepest descent method to solve the optimization problem. Finally, we did two sets of numerical simulation and the results show that the proposed algorithm can reconstruct high-quality CT images from few-views projection, which has lower Root Mean Square Error (RMSE) and higher Universal Quality Index (UQI) than Algebraic Reconstruction Technique (ART) and TV-based reconstruction method.