Search Results (29)

Background: Mushrooms have gained attention for their potential to improve brain health. We evaluated extracts of king oyster mushroom, as well as two of its bioactive compounds—ergothioneine (ERG) and N-acetyltryptamine (NAT)—for their ability to prevent microglia activation by reducing neuroinflammation and oxidative stress. Methods: HAPI microglial cells were pretreated with king oyster extracts (crude powder, acetone, ethanol, and methanol extracts at 100 μg/mL) and pure bioactive molecules of ergothioneine (ERG, 500 μM) and N-acetyl-tryptamine (NAT,50 μM) before stimulation with LPS. The effects on nitrite; TNF-α; and expressions of the inflammatory proteins iNOS, NOX2, and NLRP3 were compared with those of a blueberry extract (BB, 500 μg/mL) as a positive control. Results: All extracts and bioactive molecules significantly reduced nitrite production, similar to the BB. Overall, the best results for reducing inflammation and inflammatory protein expression were obtained with the extracts rich in NAT (acetone and ethanol), as well as pure NAT. Furthermore, through their inhibitory target effect on NLRP3, these two extracts and the bioactive compounds (NAT and ERG), like BB, are attractive therapeutic molecules to reduce mood disorders related to brain aging, due to evidence of enhanced Nucleotide-binding oligomerization domain-like receptor family pyrin domain-containing-3 (NLRP3) inflammasome activity in common neurodegenerative diseases. Further interventional studies are needed to confirm mushrooms’ brain health properties. Full article

This study examines the thermal modification (TM) of European black alder (Alnus glutinosa) wood boards measuring 1000 × 100 × 32 mm. The TM was carried out in a nitrogen atmosphere under an initial pressure of 4 bar at 160 °C for 60, 120, and 180 min, as well as at 170 °C for 30 and 60 min. The TM process resulted in mass loss and volumetric changes with shrinkage observed across all anatomical directions. Water uptake decreased significantly, with the cell wall’s total water capacity dropping from 35% to a range of 14%–27%. Dimensional stability was improved by between 21% and 61%. The TM wood showed a reduction exceeding 50% in both volumetric swelling and equilibrium moisture content relative to the unmodified specimens. A marked decline in the modulus of rupture was observed, especially in samples treated at 160 °C for 180 min and at 170 °C. Conversely, the modulus of elasticity exhibited a slight upward trend, though the changes were not statistically significant. Brinell hardness revealed a pronounced difference between the tangential and radial orientations, with the tangential surface displaying distinctly lower hardness. Chemical analysis indicated a notable increase in acetone-soluble extractives and reductions in the xylan, mannan, and acetyl groups, reflecting structural alterations in hemicelluloses. Full article

An important class of heterocyclic chemicals are pyrimidine derivatives, providing a wide spectrum of biological activities in the form of antibacterial, antifungal, anti-HIV, anti-hypertensive, anti-inflammatory, anti-cancer, anti-convulsant, anti-depressant, and anti-tuberculosis acts. The chalcone group also has a significant impact on the pharmacological activity of compounds used for therapeutic purposes, acting as antibiotics, antioxidants, and anti-cancer agents. In this research, the derivative 1-(4-(4-(dimethylamino)-2-hydroxyphenyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidin-5-yl) ethan-1-one was prepared. From the reaction of thiourea with acetyl acetone and 4-dimethylamino-2-hydroxybenzaldehyde, the product was then reacted with some aldehydes in the presence of ethanol and a little hydrochloric acid as a catalyst, after which the product was reacted with some aldehydes to prepare chalcone. The prepared derivatives were characterized by FT-IR, ¹H-NMR, and ¹³C-NMR spectra, the melting point was measured, and the biological activity of the prepared compounds as antibacterials was studied. Molecular docking also determined the anti-breast cancer potential of these derivatives by docking the prepared derivatives with PDB:3eqm protein using the MOE 2015.10 program. The prepared compounds showed good efficacy as antibacterial agents against Gram-negative bacteria at diluted concentrations. Additionally, molecular docking studies demonstrated good efficacy of some derivatives as breast cancer inhibitors, along with a study of the toxic effects of the prepared compounds using the ProTox 3.0 program prediction of toxicity of chemicals. Full article

Herein, all components of corncob residues were acetylated to synthesize an acetone-soluble resin material. Moreover, titanium oxysulfate (TiOSO₄), a low-cost intermediate for the industrial production of TiO₂, was first used as an acetylation reagent. Through optimizing reagent dosages and reaction times, above 90% of hydroxyl groups in the corncob residue can be substituted by acetyl groups. During the acetylation reaction, TiOSO₄ was transformed into TiO₂ and uniformly distributed within the acetylated corncob residue. The resulting product, owing to its solubility in acetone, can be employed to fabricate a composite film with excellent mechanical properties, achieving an increase of 85% in tensile strength and 90% in strain rate compared to commercial cellulose acetate film. By this preparation technique, the industrial-grade corncob residue as raw material can be converted to acetylated composite films. Further analysis indicates that the coexistence of acetylated lignin and TiO₂ plays a pivotal role in enhancing the mechanical properties of acetylated corncob residue composite film. Additionally, this material exhibits substantial degradation within 28 days under natural environmental conditions, whereas commercial cellulose acetate shows no significant changes even after 60 days. The present achievements are a significant breakthrough in the high-value technologies for the conversion of corncob residues. Full article

In this study, nine neo-clerodane-type diterpenoids (1–9) were isolated from the dichloromethane extract of Salvia guevarae Bedolla & Zamudio leaves. Compounds 1–6 were new natural products, and 7–9 were acetone artifacts. In addition, four neo-clerodanes diterpenoids (10–13) previously described from different sources and six triterpenoids—identified as 3β,20,25-trihydroxylupane, oleanolic acid, 3β-O-acetyl-oleanolic acid, ursolic acid, 3β-O-acetyl-betulinic acid, and 3β,28-O-diacetyl-betulin—were isolated. Additionally, five flavonoids were also isolated from the methanol extract: quercetin-3-O-β-xylopyranosyl-(1 → 2)-β-galactopyranoside, taxifolin-7-O-β-glucopyranoside, naringenin-7-O-β-glucopyranoside, a mixture of 2R and 2S eriodictyol-7-O-β-glucopyranoside, caffeic acid, the methyl ester of rosmarinic acid, and rosmarinic acid. The structure of the isolated compounds was established by spectroscopic means, mainly ¹H and ¹³C NMR, including 1D and 2D homo- and heteronuclear experiments. The absolute configuration of 1 and 10 was ascertained via an X-ray analysis, and that of the other compounds via ECD. The antiproliferative activity of some diterpenoids was determined using the sulforhodamine B method, where guevarain B (2) and 6α-hydroxy-patagonol acetonide (7) showed moderate activity against the K562 line, with IC₅₀ (μM) = 33.1 ± 1.3 and 39.8 ± 1.5, respectively. The NO inhibition in RAW 264.7 macrophage activity was also determined for some compounds, where 2-oxo-patagonal (6), 6α-hydroxy-patagonol acetonide (7), and 7α-acetoxy-ent-clerodan-3,13-dien-18,19:16,15-diolide (10) were proven to be active, with IC₅₀ (μM) of 26.4 ± 0.4, 17.3 ± 0.5, and 13.7 ± 2.0, respectively. The chemotaxonomy of Salvia guevarae is also discussed. Full article

Microplastics (MPs) are widely distributed in the environment, and they inevitably enter animal bodies during livestock and poultry farming, leading to their presence in livestock and poultry manure. However, there is limited research on the effects of different types of MPs on the anaerobic digestion (AD) performance of livestock and poultry manure. Herein, we investigated the impact of four types of MPs (polyvinyl chloride (PVC), polypropylene (PP), polyethylene (PE), and polyhydroxyalkanoate (PHA)) on AD performance using cattle manure as a substrate. Results demonstrated that the cumulative methane production in the PE group reached 5568.05 mL, exhibiting an 11.97% increase compared to the control group. Conversely, the cumulative methane production was decreased by 5.52%, 9.69%, and 14.48% in the PP, PVC, and PHA groups, respectively. Physicochemical analyses showed that MPs promoted organic matter hydrolysis on day 4 of AD, leading to the accumulation of volatile fatty acids (VFAs) in the initial stage. Specifically, the acetic acid content of PE was 44.48–92.07 mL/L higher than that of the control during the first 8 days. PE MPs also enriched microorganisms associated with methane production. The abundance of Firmicutes was enhanced by 2.89–17.57%, Methanosaeta by 8.42–12.48%, and Methanospirillum by 10.91–16.89% in comparison to the control; whereas PHA MPs decreased the abundance of Methanosaeta by 8.14–31.40%. Moreover, PHA MPs inhibited methane production by suppressing acetate kinase activity while promoting lactate dehydrogenase release from microorganisms involved in the AD process. Based on changes observed in key enzyme functional gene abundances, PHA MPs reduced acetyl-CoA carboxylase functional gene abundance, negatively affecting the acetone cleavage methanogenesis pathway. Meanwhile, PE MPs significantly increased acetate-CoA ligase abundance, thereby promoting the acetic acid methanogenesis pathway. The results provide novel insights into the influence exerted by MPs on AD performance when applied to livestock manure. Full article

Tuberculosis is a worldwide prevalent and recurring disease that contributes significantly to high mortality rates. This study aimed to investigate the antioxidant, anti-mycobacterial, and antibiofilm activities of Artemisia afra acetone crude extract. Methodology: The crude acetone extract was fractionated using column chromatography and characterized by liquid chromatography–mass spectroscopy (LC-MS). A 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging assay was used to assess the antioxidant activity. The antimycobacterial activity against Mycobacterium smegmatis was screened using bioautography, broth microdilution, and growth curve assays. Molecular docking was used to predict the possible mechanisms of action of the LC-MS-identified ligands. Crystal violet was used to screen for anti-cell adherence and biofilm inhibition activities. Results: The crude extract scavenged 77% of the free radical at 16 μg/mL. The subfraction had a lower minimum inhibitory concentration (MIC) (0.078 mg/mL) compared to the crude extract (0.313–0.833 mg/mL). The subfraction had a concentration-dependent inhibition effect (>50%) on mycobacterial cell adherence and early biofilms. However, the mature biofilms were resistant. Two propanoate compounds, [(2S)-3-[6-acetyl-4,6-dihydroxy-3-[(1R)-1-hydroxyethyl]tetrahydropyran-2-yl]-2-hydroxy-propyl] (2R)-2-amino-3-(1H-imidazol-5-yl)propanoate and 3-(6-aminopurin-9-yl)propyl 3-(2,4-dioxo-1,3-diazaspiro[4.5]decan-3-yl) propanoate, had binding energies of −5.4 kcal/mol and −6.3 kcal/mol, respectively, against the RNA polymerase binding protein. Conclusions: The results show that A. afra acetone crude extract has antioxidant and antimycobacterial activities that can be improved by fractionation. Full article

In this study, the effect of various immobilization methods on the biochemical properties of phospholipase C (PLC) from Bacillus cereus obtained from the oily soil located in Sfax, Tunisia, was described. Different supports were checked: octyl sepharose, glyoxyl agarose in the presence of N-acetyl cysteine, and Q-sepharose. In the immobilization by hydrophobic adsorption, a hyperactivation of the PLC_Bc was obtained with a fold of around 2 times. The recovery activity after immobilization on Q-sepharose and glyoxyl agarose in the presence of N-acetyl cysteine was 80% and 58%, respectively. Furthermore, the biochemical characterization showed an important improvement in the three immobilized enzymes. The performance of the various immobilized PLC_Bc was compared with the soluble enzyme. The derivatives acquired using Q-sepharose, octyl sepharose, and glyoxyl agarose were stable at 50 °C, 60 °C, and 70 °C. Nevertheless, the three derivatives were more stable in a large range of pH than the soluble enzyme. The three derivatives and the free enzyme were stable in 50% (v/v) ethanol, hexane, methanol, and acetone. The glyoxyl agarose derivative showed high long-term storage at 4 °C, with an activity of 60% after 19 days. These results suggest the sustainable biotechnological application of the developed immobilized enzyme. Full article

In this study, silver birch (Betula pendula) and Scots pine (Pinus sylvestris) wood planks (1000 × 100 × 25 mm) were thermally modified in pilot-scale equipment. Research extended our knowledge of the thermal modification (TM) process in a closed system under nitrogen pressure, as well as how process parameters affect the chemical composition and mechanical strength of wood. Various TM regimes were selected—maximum temperature (150–180 °C), modification time (30–180 min), and initial nitrogen pressure (3–6 bar). Chemical analyses were performed to assess the amount of extractives, lignin, polysaccharides and acetyl group content following the TM process. The mechanical properties of TM wood were characterized using the modulus of rupture (MOR), modulus of elasticity (MOE), and Brinell hardness. The MOR of both studied wood species following TM in nitrogen was reduced, but MOE changes were insignificant. The Brinell hardness of TM birch wood’s tangential surface was much higher than that of the radial surface, although Scots pine wood showed the opposite pattern. TM birch and pine wood specimens with the highest mass loss, acetone soluble extractive amount, and the lowest xylan and acetyl group content had the lowest MOR and Brinell hardness. Full article

The synthesis of novel heterocyclic compounds is achieved through a multi-step process involving azo dye (S1), ester (S2), and hydrazide (S3). Initially, azo dye (S1) is synthesized through the reaction between resorcinol and p-aminobenzoic acid. Subsequently, ester (S2) is formed by reacting azo dye (S1) with concentrated sulfuric acid. Hydrazide (S3) is then synthesized by reacting ester (S2) with 80% hydrazine hydrate. Further reactions of hydrazide (S3) with various anhydrides (maleic anhydride, phthalic anhydride, 3-nitrophthalic anhydride, and succinic anhydride) result in cyclization facilitated by acetic acid, yielding six-membered heterocyclic compounds. Additionally, compound S3 undergoes cyclization with acetyl acetone, ethyl acetoacetate, methyl acetoacetate, and diethyl malonate to produce five-membered heterocyclic compounds. The biological activity of these synthesized compounds is also investigated. Characterization of the prepared compounds is performed using techniques such as Fourier-Transform Infrared Spectroscopy (FT-IR), Proton Nuclear Magnetic Resonance (${}^1$HNMR), Carbon-13 Nuclear Magnetic Resonance (${}^{13}$C-NMR), and Elemental Analysis (CHNS). Full article

Magnetically soft-soft MnFe₂O₄-Fe₃O₄ core-shell nanoparticles were synthesized through a seed-mediated method using the organometallic decomposition of metal acetyl acetonates. Two sets of core-shell nanoparticles (S1 and S2) of similar core sizes of 5.0 nm and different shell thicknesses (4.1 nm for S1 and 5.7 nm for S2) were obtained by changing the number of nucleating sites. Magnetic measurements were conducted on the nanoparticles at low and room temperatures to study the shell thickness and temperature dependence of the magnetic properties. Interestingly, both core-shell nanoparticles showed similar saturation magnetization, revealing the ineffective role of the shell thickness. In addition, the coercivity in both samples displayed similar temperature dependencies and magnitudes. Signatures of spin glass (SG) like behavior were observed from the field-cooled temperature-dependent magnetization measurements. It was suggested to be due to interface spin freezing. We observed a slight and non-monotonic temperature-dependent exchange bias in both samples with slightly higher values for S2. The effective magnetic anisotropy constant was calculated to be slightly larger in S2 than that in S1. The magnetothermal efficiency of the chitosan-coated nanoparticles was determined by measuring the specific absorption rate (SAR) under an alternating magnetic field (AMF) at 200–350 G field strengths and frequencies (495.25–167.30 kHz). The S2 nanoparticles displayed larger SAR values than the S1 nanoparticles at all field parameters. A maximum SAR value of 356.5 W/g was obtained for S2 at 495.25 kHz and 350 G for the 1 mg/mL nanoparticle concentration of ferrogel. We attributed this behavior to the larger interface SG regions in S2, which mediated the interaction between the core and shell and thus provided indirect exchange coupling between the core and shell phases. The SAR values of the core-shell nanoparticles roughly agreed with the predictions of the linear response theory. The concentration of the nanoparticles was found to affect heat conversion to a great extent. The in vitro treatment of the MDA-MB-231 human breast cancer cell line and HT-29 human colorectal cancer cell was conducted at selected frequencies and field strengths to evaluate the efficiency of the nanoparticles in killing cancer cells. The cellular cytotoxicity was estimated using flow cytometry and an MTT assay at 0 and 24 h after treatment with the AMF. The cells subjected to a 45 min treatment of the AMF (384.50 kHz and 350 G) showed a remarkable decrease in cell viability. The enhanced SAR values of the core-shell nanoparticles compared to the seeds with the most enhancement in S2 is an indication of the potential for tailoring nanoparticle structures and hence their magnetic properties for effective heat generation. Full article

Selenium (Se) is an essential trace nutrient for humans and animals owing to its role in redox regulation, thyroid hormone control factors, immunity, inflammatory reactions, brain activities, and carbohydrate regulation. It is also important to support muscle development, as well as for reproductive and cardiovascular well-being. Furthermore, sulfur is known to be a healing element, due to the remarkable function of specialized and secondary S-containing compounds. The scope of the current study was to determine the impact of Se and S enrichment on the secondary metabolite accumulation and antibacterial and NO inhibition activities in green and red leaf lettuce (V1 and V2, respectively). The plants were grown in a hydroponic system supplied with different S concentrations (S0: 0, S1: 1 mM and S2: 1.5 mM K₂SO₄) via the nutrient solution and foliar-applied varying levels of Se (0, 0.2 and 2.6 µM). Electrospray ionization–quadrupole time-of-flight mass spectrometry (ESI-QTOF/MS) combined with ultra-performance liquid chromatography (UPLC) was used to identify the secondary metabolites in green and red lettuce. The results indicated that extracts of the biofortified lettuce were not cytotoxic to Vero kidney cells at the highest concentration tested of 1 mg/mL. The ESI/MS of the tentatively identified metabolites showed that the response values of 5-O-caffeoylquinic acid, cyanidin 3-O-galactoside, quercetin 3-O-(6′′-acetyl-glucoside) and quercetin 3-O-malonylglucoside were induced synergistically under higher Se and S levels in red lettuce plants. The acetone extract of red lettuce had antibacterial activity against Pseudomonas aeruginosa, with a minimum inhibitory concentration (MIC) of 0.156 and 0.625 μg/mL under S2/Se1 and S2/Se2 treatments, respectively. As with antibacterial activity, the acetone extract of green (V1) lettuce treated with adequate (S1) and higher S (S2) under Se-limiting conditions showed the ability to inhibit nitric oxide (NO) release from macrophages. NO production by macrophages was inhibited by 50% at respective concentrations of 106.1 ± 2.4 and 101.0 ± 0.6 μg/mL with no toxic effect on the cells, in response to S1 and S2, respectively, under Se-deficient conditions (Se0). Furthermore, the red cultivar (V2) exhibited the same effect as the green cultivar (V1) regarding NO inhibition, with IC₅₀ = 113.0 ± 4.2 μg/mL, in response to S1/Se2 treatments. Collectively, the promising NO inhibitory effect and antibacterial activity of red lettuce under the above-mentioned conditions might be attributed to the production of flavonoid glycosides and phenylpropanoic acid esters under the same condition. To the best of our knowledge, this is the first report to show the novel approach of the NO inhibitory effect of Se and S enrichment in food crops, as an indicator for the potential of Se and S as natural anti-inflammatory agents. Full article

This study investigates the thermal decomposition of acetyl acetonates of Ni(II) and Fe(III) via a sonochemical process at 20 kHz for 50 min. In the absence of magnetic fields the reactions of Ni(II) and Fe(III) acetyl acetonates under ultrasonic treatment produce Ni(OH)₂ and FeO(OH) nanoparticles coated with carbon. The synthesized materials with different Ni-Fe stoichiometries, Ni90-Fe10, Ni80-Fe20, and Ni50-Fe50 wt%, were subjected to catalytic activity for dye decolorization of Reactive Black 5 (RB5, 100 mg/L) at room temperature using visible radiation. The correlation between the structural and optoelectronic properties and the catalytic performance of the Ni-Fe system with different stoichiometries is reported. Full article

Cholinesterases, involved in acetylcholine catabolism in the central and peripheral nervous system, have been strongly linked with neurodegenerative diseases. Current therapeutic approaches using synthetic drugs present several side effects. Hence, there is an increasing research interest in naturally-occurring dietary polyphenols, which are also considered efficacious. Food processing by-products such as brewer’s spent grain (BSG) would be a potential bio-source of polyphenols. In this study, polyphenol-rich BSG extracts using 60% acetone and 0.75% NaOH solutions were generated, which were further subjected to liquid–liquid partitioning using various organic solvents. The water-partitioned fractions of the saponified extracts had the highest total polyphenol content (6.2 ± 2.8 mgGAE/g dw) as determined by Folin–Ciocalteu reagent, while the LC-MS/MS showed ethyl acetate fraction with the highest phenolics (2.9 ± 0.3 mg/g BSG dw). The best inhibitions of acetyl- (37.9 ± 2.9%) and butyryl- (53.6 ± 7.7%) cholinesterases were shown by the diethyl ether fraction of the saponified extract. This fraction contained the highest sum of quantified phenolics (99 ± 21.2 µg/mg of extract), and with significant (p < 0.01) inhibitory contribution of decarboxylated-diferulic acid. Amongst the standards, caffeic acid presented the highest inhibition for both cholinesterases, 25.5 ± 0.2% for acetyl- and 52.3 ± 0.8% for butyryl-cholinesterase, respectively, whilst the blends insignificantly inhibited both cholinesterases. The results showed that polyphenol-rich BSG fractions have potentials as natural anti-cholinesterase agents. Full article

The antioxidant activities of Japanese knotweed rhizome bark extracts, prepared with eight different solvents or solvent mixtures (water, methanol, 80% methanol_(aq), acetone, 70% acetone_(aq), ethanol, 70% ethanol_(aq), and 90% ethyl acetate_(aq)), were determined using a 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical-scavenging assay. Low half maximal inhibitory concentration (IC₅₀) values (2.632–3.720 µg mL⁻¹) for all the extracts were in the range of the IC₅₀ value of the known antioxidant ascorbic acid at t₀ (3.115 µg mL⁻¹). Due to the highest extraction yield (~44%), 70% ethanol_(aq) was selected for the preparation of the extract for further investigations. The IC₅₀ value calculated for its antioxidant activity remained stable for at least 14 days, while the IC₅₀ of ascorbic acid increased over time. The stability study showed that the container material was of great importance for the light-protected storage of the ascorbic acid_(aq) solution in a refrigerator. Size exclusion–high-performance liquid chromatography (SEC-HPLC)–UV and reversed phase (RP)-HPLC-UV coupled with multistage mass spectrometry (MSⁿ) were developed for fractionation of the 70% ethanol_(aq) extract and for further compound identification, respectively. In the most potent antioxidant SEC fraction, determined using an on-line post-column SEC-HPLC-DPPH assay, epicatechin, resveratrol malonyl hexoside, and its in-source fragments (resveratrol and resveratrol acetyl hexoside) were tentatively identified by RP-HPLC-MSⁿ. Moreover, epicatechin was additionally confirmed by two orthogonal methods, SEC-HPLC-UV and high-performance thin-layer chromatography (HPTLC) coupled with densitometry. Finally, the latter technique enabled the identification of (−)-epicatechin. (−)-Epicatechin demonstrated potent and stable time-dependent antioxidant activity (IC₅₀ value ~1.5 µg mL⁻¹) for at least 14 days. Full article