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With the climate constantly changing, plants suffer more frequently from various abiotic and biotic stresses. However, they have evolved biosynthetic machinery to survive in stressful environmental conditions. Flavonoids are involved in a variety of biological activities in plants, which can protect plants from different biotic (plant-parasitic nematodes, fungi and bacteria) and abiotic stresses (salt stress, drought stress, UV, higher and lower temperatures). Flavonoids contain several subgroups, including anthocyanidins, flavonols, flavones, flavanols, flavanones, chalcones, dihydrochalcones and dihydroflavonols, which are widely distributed in various plants. As the pathway of flavonoid biosynthesis has been well studied, many researchers have applied transgenic technologies in order to explore the molecular mechanism of genes associated with flavonoid biosynthesis; as such, many transgenic plants have shown a higher stress tolerance through the regulation of flavonoid content. In the present review, the classification, molecular structure and biological biosynthesis of flavonoids were summarized, and the roles of flavonoids under various forms of biotic and abiotic stress in plants were also included. In addition, the effect of applying genes associated with flavonoid biosynthesis on the enhancement of plant tolerance under various biotic and abiotic stresses was also discussed.

Saponins are amphiphilic molecules consisting of carbohydrate and either triterpenoid or steroid aglycone moieties and are noted for their multiple biological activities—Fungicidal, antimicrobial, antiviral, anti-inflammatory, anticancer, antioxidant and immunomodulatory effects have all been observed. Saponins from natural sources have long been used in herbal and traditional medicines; however, the isolation of complexed saponins from nature is difficult and laborious, due to the scarce amount and structure heterogeneity. Chemical synthesis is considered a powerful tool to expand the structural diversity of saponin, leading to the discovery of promising compounds. This review focuses on recent developments in the structure optimization and biological evaluation of synthetic triterpenoid and steroid saponin derivatives. By summarizing the structure–activity relationship (SAR) results, we hope to provide the direction for future development of saponin-based bioactive compounds.

Multiferroic materials, which simultaneously exhibit ferroelectric and magnetic orders, provide a unique platform to explore the interplay between charge and spin degrees of freedom for spintronics applications. These materials enable novel functionalities and applications, making them a focal point of research in condensed matter physics and materials science. This Editorial highlights current stage of multiferroic research and discusses future directions in this rapidly evolving field.

Vitellogenin receptor (VgR) plays a pivotal role in ovarian vitellogenin (Vg) uptake and vertical transmission of pathogenic microbes and Wolbachia symbionts. However, the regulatory mechanisms of VgR action as an endocytic receptor and translocation from oocyte cytoplasm to the membrane remain poorly understood. Here, by using the migratory locust Locusta migratoria as a model system, we report that juvenile hormone (JH) promotes VgR phosphorylation at Ser1361 in the second EGF-precursor homology domain. A signaling cascade including GPCR, PLC, extracellular calcium, and PKC-ι is involved in JH-stimulated VgR phosphorylation. This post-translational regulation is a prerequisite for VgR binding to Vg on the external surface of the oocyte membrane and subsequent VgR/Vg endocytosis. Acidification, a condition in endosomes, induces VgR dephosphorylation along with the dissociation of Vg from VgR. Phosphorylation modification is also required for VgR recycling from oocyte cytoplasm to the membrane. Additionally, VgR phosphorylation and its requirement for Vg uptake and VgR recycling are evolutionarily conserved in other representative insects including the cockroach Periplaneta americana and the cotton bollworm Helicoverpa armigera. This study fills an important knowledge gap of low-density lipoprotein receptors in posttranslational regulation, endocytosis, and intracellular recycling.

The low-density lipoprotein (LDL) is a major cholesterol carrier in circulation and is internalized into cells through LDL receptor (LDLR)-mediated endocytosis. The LDLR protein is highly expressed in the steroidogenic organs and LDL cholesterol is an important source for steroidogenesis. Cholesterol must be transported into the mitochondria, where steroid hormone biosynthesis initiates. However, how LDL cholesterol is conveyed to the mitochondria is poorly defined. Here, through genome-wide small hairpin RNA screening, we find that the outer mitochondrial membrane protein phospholipase D6 (PLD6), which hydrolyses cardiolipin to phosphatidic acid, accelerates LDLR degradation. PLD6 promotes the entrance of LDL and LDLR into the mitochondria, where LDLR is degraded by mitochondrial proteases and LDL-carried cholesterol is used for steroid hormone biosynthesis. Mechanistically, the outer mitochondrial membrane protein CISD2 binds to the cytosolic tail of LDLR and tethers LDLR + vesicles to the mitochondria. The fusogenic lipid phosphatidic acid generated by PLD6 facilitates the membrane fusion of LDLR + vesicles with the mitochondria. This intracellular transport pathway of LDL–LDLR bypasses the lysosomes and delivers cholesterol to the mitochondria for steroidogenesis. Zhou et al. describe an intracellular transport pathway of low-density lipoprotein (LDL)–LDL receptor from the plasma membrane that bypasses lysosomes and delivers cholesterol to mitochondria for steroidogenesis.

Let H be a separable Hilbert space and let { x n } be a sequence in H that does not contain any zero elements. We say that { x n } is a Bessel-normalizable or frame-normalizable sequence if the normalized sequence { x n ‖ x n ‖ } is a Bessel sequence or a frame for H , respectively. In this paper, several necessary and sufficient conditions for sequences to be frame-normalizable and not frame-normalizable are proved. Perturbation theorems for frame-normalizable sequences are also proved. As applications, we show that the Balazs–Stoeva conjecture holds for Bessel-normalizable sequences. Finally, we apply our results to partially answer the open question raised by Aldroubi et al. as to whether the iterative system { A n x ‖ A n x ‖ } n ≥ 0 , x ∈ S associated with a normal operator A : H → H and a countable subset S of H , is a frame for H . In particular, if S is finite, then we are able to show that { A n x ‖ A n x ‖ } n ≥ 0 , x ∈ S is not a frame for H whenever { A n x } n ≥ 0 , x ∈ S is a frame for H .

The outbreak of COVID-19 caused by SARS-CoV-2 has resulted in more than 50 million confirmed cases and over 1 million deaths worldwide as of November 2020. Currently, there are no effective antivirals approved by the Food and Drug Administration to contain this pandemic except the antiviral agent remdesivir. In addition, the trimeric spike protein on the viral surface is highly glycosylated and almost 200,000 variants with mutations at more than 1,000 positions in its 1,273 amino acid sequence were reported, posing a major challenge in the development of antibodies and vaccines. It is therefore urgently needed to have alternative and timely treatments for the disease. In this study, we used a cell-based infection assay to screen more than 3,000 agents used in humans and animals, including 2,855 small molecules and 190 traditional herbal medicines, and identified 15 active small molecules in concentrations ranging from 0.1 nM to 50 μM. Two enzymatic assays, along with molecular modeling, were then developed to confirm those targeting the virus 3CL protease and the RNA-dependent RNA polymerase. Several water extracts of herbal medicines were active in the cell-based assay and could be further developed as plant-derived anti–SARS-CoV-2 agents. Some of the active compounds identified in the screen were further tested in vivo, and it was found that mefloquine, nelfinavir, and extracts of Ganoderma lucidum (RF3), Perilla frutescens, and Mentha haplocalyx were effective in a challenge study using hamsters as disease model.

Although several laser-plasma-based methods have been proposed for generating energetic electrons, positrons and γ-photons, manipulation of their microstructures is still challenging, and their angular momentum control has not yet been achieved. Here, we present and numerically demonstrate an all-optical scheme to generate bright GeV γ-photon and positron beams with controllable angular momentum by use of two counter-propagating circularly-polarized lasers in a near-critical-density plasma. The plasma acts as a 'switching medium', where the trapped electrons first obtain angular momentum from the drive laser pulse and then transfer it to the γ-photons via nonlinear Compton scattering. Further through the multiphoton Breit-Wheeler process, dense energetic positron beams are efficiently generated, whose angular momentum can be well controlled by laser-plasma interactions. This opens up a promising and feasible way to produce ultra-bright GeV γ-photons and positron beams with desirable angular momentum for a wide range of scientific research and applications.

The understanding of the mechanisms that govern water spontaneous imbibition in mixed wetting capillary channels plays a significant role in operating the oil extraction and energy replenishment for the tight oil reservoirs. In this work, the conservative form phase-field model together with the Navier–Stokes equation is employed to investigate the influence of the mixed wetting distribution and the wetting degree on the imbibition oil recovery effects and microscopic flow characteristics. Results indicate that there exist different oil detachment modes of spontaneous imbibition, and these modes are determined by the coupled effect of mixed wetting fraction and contact angle size. For the mixed wetting capillary with strong oil wetting, when fw is low, spontaneous imbibition can only partially detach the oil. Low fw slows down the fluid flow velocity and leads to the small imbibition oil recovery rate. After that, the influence of the surface contact angle size of the mixed wetting capillary is discussed. For the complete detachment mode, the capillary tube presents a form of water phase saturated filling, achieving the optimal imbibition oil recovery effect. For the mixed wetting capillary tube with the combination of weak water wetting and strong oil wetting (i.e., θw = 75° and θo = 165°), local spontaneous imbibition turbulence can only detach very little oil at the inlet of the water wetting area, ultimately achieving a recovery efficiency of less than 10%. This work illuminates the spontaneous imbibition oil recovery mechanisms and flow potentiality for the different mixed wetting capillary channels.

The knowledge that natural products (NPs) are potent and selective modulators of important biomacromolecules (e.g., DNA and proteins) has inspired some of the world’s most successful pharmaceuticals and agrochemicals. Notwithstanding these successes and despite a growing number of reports on naturally occurring pairs of enantiomers, this area of NP science still remains largely unexplored, consistent with the adage “If you don’t seek, you don’t find”. Statistically, a rapidly growing number of enantiomeric NPs have been reported in the last several years. The current review provides a comprehensive overview of recent records on natural enantiomers, with the aim of advancing awareness and providing a better understanding of the chemical diversity and biogenetic context, as well as the biological properties and therapeutic (drug discovery) potential, of enantiomeric NPs.