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Lipopolysaccharide (LPS) is an important pathogenic factor and plays a key role in human diseases such as fever, shock, and sepsis. Blocking the toxicity of LPS through antagonism is considered the best choice for the treatment of LPS-induced diseases. In this research, nucleic acid aptamer LA27, which was previously selected and optimized by our group, was used as an LPS inhibitor to treat human HepG2 cells stimulated by LPS from four different sources (StLPS, EcoliLPS, PaLPS, and SeLPS): the levels of expression of three inflammatory cytokines factors (TNF-α, IL-1β, and IL-6) were evaluated by ELISA on LA27-treated and untreated cells incubated for 12 h with LPS. The results of the assays indicated that LA27 exhibited considerable anti-inflammatory activity. The binding site and interactions between aptamer LA27 and LPSs were also simulated using Molecular Operating Environment (MOE) 2018 software. MOE simulation results showed that, under a combination of the hydrophobic interaction, hydrogen bonding, and electrostatic interactions, the fatty acid chain of LPS could interact with the wide hydrophobic region of the aptamer, constituting its major groove, and formed stable complex of T-type. The present research indicated that LA27 might be a potential therapeutic agent for sepsis and other diseases, which provides a new path for the development of LPS antagonists.

Carbonation treatment (CT) by alkaline fly ash (FA) affects the stability of potentially toxic elements (PTEs). This study investigated the leachability and environmental risk of six PTEs contained in FA during natural and accelerated carbonation (NC, AC) using two typical leaching scenarios with distilled water (DW) and acetic acid (AA). The leaching of Pb/Cu/Cr/Ni in solidified/stabilized FA decreased due to CT in DW leaching, but the leaching of Pb/Zn/Cu/Cd increased due to CT in AA leaching. The leaching of the six PTEs (especially Pb/Cd) in AA leaching was significantly higher than that in DW leaching. CT was a promoting factor to increase the environmental risk level of PTEs in FA leachate, especially in AA leaching with H+ input. In the early stage of NC, under DW leaching tests, the environmental risk level of PTEs in FA leachate can be weakened due to the formation of carbonate minerals in the FA matrix. However, excessive NC increases the environmental risk of leached PTEs due to the decalcification of carbonate minerals. Both NC and AC increased the potential environmental risk of PTEs contained in the carbonated FA matrix. The nucleation and dissolution of carbonate minerals were interdependent with the immobilization and leaching of PTEs, which played a dominant role in the CT and leaching tests respectively. They jointly affected the occurrence behavior of PTEs in the FA matrix in CT tests and the leachability of PTEs in leaching tests. This study demonstrates that it is more scientific to evaluate the leachability of PTEs in carbonated FA according to the actual disposal scenarios.

Gamma-aminobutyric acid (GABA), a nonproteinous amino acid with some benefits on human health, is synthesized by GABA-shunt and the polyamine degradation pathway in plants. The regulation of Ca2+ and aminoguanidine on GABA accumulation in germinating soybean (Glycine max L.) under hypoxia-NaCl stress was investigated in this study. Exogenous Ca2+ increased GABA content significantly by enhancing glutamate decarboxylase gene expression and its activity. Addition of ethylene glycol tetra-acetic acid into the culture solution reduced GABA content greatly due to the inhibition of glutamate decarboxylase activity. Aminoguanidine reduced over 85% of diamine oxidase activity, and 33.28% and 36.35% of GABA content in cotyledon and embryo, respectively. Under hypoxia–NaCl stress, the polyamine degradation pathway contributed 31.61–39.43% of the GABA formation in germinating soybean.

Alpha-lipoic acid (ALA), a naturally occurring compound, exerts powerful protective effects in numerous cardiovascular disease models. However, the pharmacological property of ALA on cardiac hypertrophy has not been well investigated. The present study was carried out to determine whether ALA exerts a direct anti-hypertrophic effect in cultured cardiomyocytes and whether it modifies the hypertrophic process in vivo. Furthermore, we determined the potential underlying mechanisms for these actions. Treatment of cardiomyocytes with phenylephrine (PE) for 24 h produced a marked hypertrophic effect as evidenced by significantly increased in ANF and BNP mRNA levels, as well as cell surface area. These effects were attenuated by ALA in a concentration-dependent manner with a complete inhibition of hypertrophy at a concentration of 100 µg/mL. PE-induced cardiomyocyte hypertrophy was associated with increased mRNA and protein levels of C/EBPβ, which were inhibited by pretreatment with ALA. However, when cardiomyocytes were co-transfected with C/EBPβ, ALA failed to inhibit hypertrophic responses. Upregulation of C/EBPβ expression was also evident in rats subjected to 4 weeks of coronary artery ligation (CAL). However, rats treated with ALA demonstrated markedly reduced hemodynamic and hypertrophic responses, which were accompanied by attenuation of upregulation of C/EBPβ. Taken together, our results revealed a robust anti-hypertrophic and anti-remodeling effect of ALA, which is mediated by inhibition of C/EBPβ activation.

Reduced glutathione (GSH) from fermentation broth of Saccharomyces cerevisiae was extracted with ethanol without disruption of the cells. The effects of ethanol concentration, extraction temperature and extraction time were assessed by using 2(3) full factorial designs (FFD). Preliminary studies showed that ethanol concentration had the most influence on GSH yield by ethanol extraction, based on the first order regression coefficients derived using MINITAB software, and an optimal ethanol concentration (25%, v/v) was obtained. However, compared to the conventional extraction technique (hot water extraction), there was no significant advantage in yield of GSH from yeast cells using ethanol extraction under these optimized conditions. But ethanol extraction has several advantages, such as lower energy consumption and lower protein concentration of extraction broth, which may reduce the complexity and cost of the purification process. Hence, ethanol extraction which does not disrupt yeast cells could be an inexpensive, simple and efficient alternative to conventional extraction techniques in the GSH industry.

An on-line monitoring of viable-cell mass in high-cell-density fed-batch cultivations of Saccharomyces cerevisiae grown on an industrial complex medium was performed with an in situ capacitance probe fitted to a 50-l fermentor. Conventional off-line biomass determinations of several parameters, including dry cell weight (DCW), optical density at 600 nm wavelength (OD(600)), packed mycelial volume (PMV) and number of colony forming units (CFU), were performed throughout the bioprocess and then compared with on-line viable-cell concentrations measured using a capacitance probe. Capacitance versus viable biomass and all off-line biomass assay values were compared during glutathione fermentation in industrial complex culture media. As a result, the relationship between the number of colony forming units and capacitance with a correlation coefficient (R) of 0.995 was achieved. Simultaneously, compared with those determined by at-line indirect estimation methods including oxygen uptake rate (OUR) and carbon dioxide evolution rate (CER), the specific growth rates estimated by on-line capacitance measurement could be more reliable during glutathione fermentation. Therefore, it is concluded that a capacitance probe is a practical tool for real-time viable biomass monitoring in high-cell-density fed-batch cultivation in a complex medium.