The anti-aging effects of Chlorella polysaccharide extract in Caenorhabditis elegans.

Chlorella has a variety of biological activities, and it is worth further exploring its pharmacological effects. In this study, we investigated the antioxidant and anti-ageing activities of Chlorella polysaccharide extract (CPE). Further studies revealed that CPE exhibited anti-ageing, and antioxidant activities in vivo, including an extended Caenorhabditis elegans stress resistance, decreased deposition of lipofuscin, and reduced effects of amyloid ß protein on mobility, decreased levels of reactive oxygen species and increased activity of antioxidant enzymes. Moreover, it dramatically increased the expression of anti-stress and longevity genes and reduced the expression of ageing-related genes; therefore, it was hypothesised that the mechanism of the age-delaying effect of CPE was related to the insulin signalling pathway. In summary, CPE could delay ageing and provide a new avenue for the application and development of CPE.

A Hadal Streptomyces-Derived Echinocandin Acylase Discovered through the Prioritization of Protein Families.

Naturally occurring echinocandin B and FR901379 are potent antifungal lipopeptides featuring a cyclic hexapeptide nucleus and a fatty acid side chain. They are the parent compounds of echinocandin drugs for the treatment of severe fungal infections caused by the Candida and Aspergilla species. To minimize hemolytic toxicity, the native fatty acid side chains in these drug molecules are replaced with designer acyl side chains. The deacylation of the N-acyl side chain is, therefore, a crucial step for the development and manufacturing of echinocandin-type antibiotics. Echinocandin E (ECE) is a novel echinocandin congener with enhanced stability generated via the engineering of the biosynthetic machinery of echinocandin B (ECB). In the present study, we report the discovery of the first echinocandin E acylase (ECEA) using the enzyme similarity tool (EST) for enzymatic function mining across protein families. ECEA is derived from Streptomyces sp. SY1965 isolated from a sediment collected from the Mariana Trench. It was cloned and heterologously expressed in S. lividans TK24. The resultant TKecea66 strain showed efficient cleavage activity of the acyl side chain of ECE, showing promising applications in the development of novel echinocandin-type therapeutics. Our results also provide a showcase for harnessing the essentially untapped biodiversity from the hadal ecosystems for the discovery of functional molecules.

Cleaning efficacy of EDDY versus ultrasonically-activated irrigation in root canals: a systematic review and meta-analysis.

BACKGROUND: Ultrasonically-activated irrigation (UAI) is effective in root canal irrigation but may damage canal walls. EDDY is a sonic activation system with flexible working tips that cause no harm to dentinal walls. This review explores the intracanal cleaning efficacy of EDDY compared with UAI in vitro. METHODS: The systematic review was registered in the PROSPERO database (CRD42021235826). A literature search was conducted in six electronic databases. In vitro studies that compared the removal of smear layer, debris, soft tissue or microbes in root canals between EDDY and UAI were included. Data extraction and quality assessment were performed. Meta-analyses were conducted on smear layer removal and debris elimination with the standardized mean difference (SMD). Heterogeneity was measured using the I2 test and the Chi2 test. The random-effect model was used when I2 > 50%, or p < 0.1, otherwise the fixed-effect model was applied. The level of significance was set at p < 0.05. RESULTS: 19 articles were included in this systematic review and 7 articles were included in meta-analyses. Meta-analyses on smear layer removal showed unimportant differences between EDDY and UAI at any canal third (coronal [SMD = 0.08, 95% confidence interval (95%CI): -0.29 to 0.45; p = 0.44, I2 = 0%]; middle [SMD = 0.02, 95% CI: -0.44 to 0.47; p = 0.94, I2 = 0%]; apical [SMD = 0.01, 95%CI: -0.35 to 0.38; p = 0.70, I2 = 0%]). Meta-analyses on debris removal evaluated by scanning electron microscope (coronal [SMD = 0.03, 95% CI: -0.41 to 0.46; p = 0.27, I2 = 23%]; middle [SMD = -0.24, 95% CI: -0.83 to 0.35; p = 0.80, I2 = 0%]; apical [SMD = 0.24, 95%CI: -0.20 to 0.67; p = 0.36, I2 = 2%]) and micro-CT (SMD = 0.36, 95% CI: -0.67 to 1.40; p = 0.03, I2 = 70%) both found insignificant differences. No meta-analysis was undertaken on soft-tissue removal and disinfection due to the various study designs, but the qualitative analyses implied that EDDY achieved similar performance to UAI in both aspects. CONCLUSIONS: Limited evidence indicated that EDDY was comparable to UAI in removing smear layer, debris, soft tissue and microbes ex vivo. Considering UAI may damage canal walls, EDDY might be a substitute for UAI in irrigation activation. But more randomized clinical trials are required to explore the clinical extrapolation of the results in this review.

Tunable Redox Mediators for Li-O2 Batteries Based on Interhalide Complexes.

Li-O2 batteries can provide significantly higher gravimetric energy density than Li-ion batteries, but their practical use is limited by a number of fundamental issues associated with oxidizing discharge products such as Li2O2 and LiOH during charging. Soluble inorganic redox mediators (RMs) like LiI and LiBr have been shown to enhance round-trip efficiency where different solvents can greatly shift the redox potential of the RMs, significantly altering the overpotential during charging, as well as their oxidizing power against the discharge product. Unfortunately, other design requirements like (electro)chemical stability with the electrode as well as reactive discharge products greatly constrain the selection of solvent, making it impractical to additionally design the solvent to provide optimal RM performance. In this work, we demonstrate that interhalide RMs based on LiI/LiBr and LiI/LiCl mixtures can enable tuning of the oxidizing power of the RM in a given solvent. I-Br interhalides I2Br- to IBr2- showed increasing chemical oxidizing power toward Li2O2 and LiOH with increasing Br, and DEMS measurements during charging of Li-O2 cells demonstrated that these I-Br interhalide RMs led to increased O2 evolution with respect to LiI and reduced charging potential and CO2 evolution with respect to LiBr.

MicroRNA-760 inhibits cell viability and migration through down-regulating BST2 in gastric cancer.

Gastric cancer is one of the most common types of carcinoma with a threat to global health. MicroRNA-760 (miR-760) was significantly down-regulated in the primary tumour of patients with advanced gastric cancer. However, the role of miR-760 in gastric cancer is still unclear. Herein, miR-760 was down-regulated in gastric cancer tissues. Moreover, miR-760 overexpression and knockdown were conducted in gastric cancer cells (MGC-803 and SGC-7901) in vitro. The in vitro functional assays proved that miR-760 overexpression reduced cell viability, cell cycle, migration and invasion, promoted apoptosis and suppressed MMP activity in MGC-803 cells. Conversely, miR-760 knockdown led to the opposite in SGC-7901 cells. Notably, bone marrow stromal antigen 2 (BST2) was verified as a target gene of miR-760. MiR-760 mimics down-regulated BST2 level in gastric cancer tissues and in MGC-803 cells, whereas miR-760 inhibitor up-regulated its level in SGC-7901 cells. MiR-760-regulated cell properties through reduction of BST2. In addition, miR-760 inhibited tumourigenesis in a nude mouse xenograft model in vivo. In conclusion, our results demonstrated that miR-760 exhibited a suppressive role in gastric cancer via inhibiting BST2, indicating that miR-760/BST2 axis may provide promising therapeutic target for gastric cancer.

Z-scheme CdS/CQDs/g-C3N4 composites with visible-near-infrared light response for efficient photocatalytic organic pollutant degradation.

We have successfully synthesized novel Z-scheme CdS/CQDs/g-C3N4 composites with visible-near-infrared light response for the photocatalytic degradation of rhodamine B (RhB), methylene Blue (MB) and phenol. Based on the energy band matching theory, CdS was coupled with g-C3N4 using carbon quantum dots (CQDs) as the electron mediator to form the Z-scheme heterojunctions through a simple calcination process. Compared with the single-phase and binary composites, the Z-scheme CdS/CQDs/g-C3N4 composites not only exhibited enhanced photocatalytic activity and photostability but also realized near-infrared light response. CQDs, as the electron mediator, can shuttle the electrons in the CdS/CQDs/g-C3N4 interface via the Z-scheme electron transfer pathway, which lead to improvements in charge separation and oxidizability of the composites. The Z-scheme electron transfer was verified using various techniques, including PL, EIS, EPR and transient photocurrent response. The mechanism of Z-scheme charge transfer was also proposed for the improved photocatalytic RhB degradation activity. In addition, CQDs can capture near-infrared light through the upconversion fluorescence property, ameliorating the broad- spectrum photocatalytic competence. Therefore, the Z-scheme heterojunction with visible-near-infrared light response was utilized to improve charge separation, oxidizability and solar energy utilization, as well as to provide new insights for the construction of CQDs-based Z-scheme composites for photocatalysis applications.

An N-Heterocyclic-Carbene-Derived Distonic Radical Cation.

We present the discovery of a novel radical cation formed through one-electron oxidation of an N-heterocyclic carbene-carbodiimide (NHC-CDI) zwitterionic adduct. This compound possesses a distonic electronic structure (spatially separate spin and charge regions) and displays persistence under ambient conditions. We demonstrate its application in a redox-flow battery exhibiting minimal voltage hysteresis, a flat voltage plateau, high Coulombic efficiency, and no performance decay for at least 100 cycles. The chemical tunability of NHCs and CDIs suggests that this approach could provide a general entry to redox-active NHC-CDI adducts and their persistent radical ions for various applications.

Molecular Design of Stable Sulfamide- and Sulfonamide-based Electrolytes for Aprotic Li-O2 Batteries.

Electrolyte instability is one of the most challenging impediments to enabling Lithium-Oxygen (Li-O2) batteries for practical use. The use of physical organic chemistry principles to rationally design new molecular components may enable the discovery of electrolytes with stability profiles that cannot be achieved with existing formulations. Here, we report on the development of sulfamide- and sulfonamide-based small molecules that are liquids at room temperature, capable of dissolving reasonably high concentration of Li salts (e.g., LiTFSI), and are exceptionally stable under the harsh chemical and electrochemical conditions of aprotic Li-O2 batteries. In particular, N,N-dimethyl-trifluoromethanesulfonamide was found to be highly resistant to chemical degradation by peroxide and superoxide, stable against electrochemical oxidation up to 4.5 VLi, and stable for > 90 cycles in a Li-O2 cell when cycled at < 4.2 VLi. This study provides guiding principles for the development of next-generation electrolyte components based on sulfamides and sulfonamides.

Non-covalent interactions in electrochemical reactions and implications in clean energy applications.

Understanding and controlling non-covalent interactions associated with solvent molecules and redox-inactive ions provide new opportunities to enhance the reaction entropy changes and reaction kinetics of metal redox centers, which can increase the thermodynamic efficiency of energy conversion and storage devices. Here, we report systematic changes in the redox entropy of one-electron transfer reactions including [Fe(CN)6]3-/4-, [Fe(H2O)6]3+/2+ and [Ag(H2O)4]+/0 induced by the addition of redox inactive ions, where approximately twenty different known structure making/breaking ions were employed. The measured reaction entropy changes of these redox couples were found to increase linearly with higher concentration and greater structural entropy (having greater structure breaking tendency) for inactive ions with opposite charge to the redox centers. The trend could be attributed to the altered solvation shells of oxidized and reduced redox active species due to non-covalent interactions among redox centers, inactive ions and water molecules, which was supported by Raman spectroscopy. Not only were these non-covalent interactions shown to increase reaction entropy, but they were also found to systematically alter the redox kinetics, where increasing redox reaction energy changes associated with the presence of water structure breaking cations were correlated linearly with the greater exchange current density of [Fe(CN)6]3-/4-.

Correction: Revealing instability and irreversibility in nonaqueous sodium-O2 battery chemistry.

Correction for 'Revealing instability and irreversibility in nonaqueous sodium-O2 battery chemistry' by Sayed Youssef Sayed et al., Chem. Commun., 2016, 52, 9691-9694.

The effect of water on discharge product growth and chemistry in Li-O2 batteries.

Understanding what controls Li-O2 battery discharge product chemistry and morphology is key to enabling its practical deployment as a low-cost, high-specific-energy energy conversion technology. Several studies have recently shown that the addition of substantial quantities (hundreds to thousands ppm) of water and weak acids to dimethoxyethane (DME)-based electrolytes can significantly increase Li-O2 battery discharge capacity, without substantially changing the discharge product chemistry, which remains Li2O2. The exact mechanisms behind these device-level improvements, however, are not yet understood. In this study, we show that the presence of water in a DME-based electrolyte decreases the rate of Li2O2 nucleation on the electrode surface during Li-O2 battery discharge, using potentiostatic electrochemical measurements, and direct, ex situ observations of Li2O2 particles. We also show that adding water to an acetonitrile (MeCN)-based electrolyte results in LiOH upon discharge, as opposed to only Li2O2. Using first principles calculations, we propose that this change in discharge product chemistry is attributable to increased proton availability, as shown by a lower pKa for water in MeCN than in DME. This study combines kinetic and morphological analyses with first principles calculations, and elucidates relationships among electrolyte composition, discharge product chemistry and growth mechanisms for the rational design of efficient metal-air batteries.

Revealing instability and irreversibility in nonaqueous sodium-O2 battery chemistry.

Charging kinetics and reversibility of Na-O2 batteries can be influenced greatly by the particle size of NaO2 formed upon discharge, and exposure time (reactivity) of NaO2 to the electrolyte. Micrometer-sized NaO2 cubes formed at high discharge rates were charged at smaller overpotentials compared to nanometer-sized counterparts formed at low rates.

MTA1 promotes proliferation and invasion in human gastric cancer cells.

Although metastasis-associated protein 1 (MTA1) has been widely linked to tumor metastasis, the relevant mechanisms remain to be elucidated, especially in gastric cancer. The aim of this study was to examine whether the MTA1 gene is associated with the process of proliferation and invasion by regulating several molecular targets in gastric cancer. MTA1 expression in 61 gastric cancer tissue and adjacent noncancerous tissues was analyzed by immunohistochemistry. The prognostic value of MTA1 for overall survival and disease-free survival was determined by Kaplan-Meier estimates, and the significance of differences between curves was evaluated by the log-rank test. Furthermore, overexpression of MTA1 in SGC7901 and BGC823 cells promoted cell cycle progression, cell adhesion, and cell invasion. Our study found that MTA1 is overexpressed in gastric cancers, which contributes to malignant cell growth by facilitating cell cycle progression through upregulation of cyclin D1 and accelerates the migration and invasion of human gastric cancer cells by regulating expression of fibronectin and MMP2/MMP9. Taken together, MTA1 was involved in the pathogenesis of gastric cancer and might be a candidate therapeutic target in gastric cancer.

Multi-Gaussian fitting for pulse waveform using Weighted Least Squares and multi-criteria decision making method.

Analysis of pulse waveform is a low cost, non-invasive method for obtaining vital information related to the conditions of the cardiovascular system. In recent years, different Pulse Decomposition Analysis (PDA) methods have been applied to disclose the pathological mechanisms of the pulse waveform. All these methods decompose single-period pulse waveform into a constant number (such as 3, 4 or 5) of individual waves. Furthermore, those methods do not pay much attention to the estimation error of the key points in the pulse waveform. The estimation of human vascular conditions depends on the key points' positions of pulse wave. In this paper, we propose a Multi-Gaussian (MG) model to fit real pulse waveforms using an adaptive number (4 or 5 in our study) of Gaussian waves. The unknown parameters in the MG model are estimated by the Weighted Least Squares (WLS) method and the optimized weight values corresponding to different sampling points are selected by using the Multi-Criteria Decision Making (MCDM) method. Performance of the MG model and the WLS method has been evaluated by fitting 150 real pulse waveforms of five different types. The resulting Normalized Root Mean Square Error (NRMSE) was less than 2.0% and the estimation accuracy for the key points was satisfactory, demonstrating that our proposed method is effective in compressing, synthesizing and analyzing pulse waveforms.

Determination of proton affinities and acidity constants of sugars.

Proton transfer reactions play a key role in the conversion of biomass derived sugars to chemicals. In this study, we employ high level ab initio theoretical methods, in tandem with solvation effects to calculate the proton affinities (PA) and acidity constants (pKa) of various d-glucose and d-fructose tautomers (protonation-deprotonation processes). In addition, we compare the theoretically derived pH values of sugar solutions against experimentally measured pH values in our lab. Our results demonstrate that the protonation of any of the O atoms of the sugars is thermodynamically preferred without any significant variation in the PA values. Intramolecular hydrogen transfers, dehydration reactions, and ring-opening processes were observed, resulting from the protonation of specific hydroxyl groups on the sugars. Regarding the deprotonation processes (pKa), we found that the sugars' anomeric hydroxyls exhibit the highest acidity. The theoretically calculated pH values of sugar solutions are in excellent agreement with experimental pH measurements at low sugar concentrations. At higher sugar concentrations the calculations predict less acidic solutions than the experiments. In this case, we expect the sugars to act as solvents increasing the proton solvation energy and the acidity of the solutions. We demonstrated through linear relationships that the pKa values are correlated with the relative stability of the conjugate bases. The latter is related to hydrogen bonding and polarization of the C-O(-) bond. A plausible explanation for the good performance of the direct method in calculating the pKa values of sugars can be the presence of intramolecular hydrogen bonds on the conjugate base. Both theory and experiments manifest that fructose is a stronger acid than glucose, which is of significant importance in self-catalyzed biomass-relevant dehydration reactions.