Omega-3 fatty acids concentrate production by enzyme-catalyzed ethanolysis of supercritical CO<Subscript>2</Subscript> extracted oyster oil

The separation of oil by a suitable technique from the Pacific oyster muscle is important for the utilization of the oil as a ω-3 polyunsaturated fatty acids (ω-3 PUFAs) source and production of bio-functional peptides/ oligosaccharides from oil-free residue. This study was conducted to prepare ω-3 PUFAs concentrate from supercritical carbon dioxide (SC-CO₂) extracted Pacific oyster oil by enzyme-catalyzed ethanolysis reactions. SC-CO₂ extractions were done at different temperatures and pressures to optimize suitable extraction conditions and extracted oils were compared with Soxhlet (n-hexane) extracted oil to evaluate the yield and quality. Oil extracted by SC-CO₂ at optimized conditions was used for ethanolysis reaction catalyzed by immobilized sn-1,3 specific lipases, namely Novozymes-435, Lipozyme TLIM, and Lipozyme RMIM to produce 2-monoacylglycerols (2-MAG) rich in ω-3 PUFAs. The optimum temperature and pressure for SC-CO₂ extractions of oyster oil was 50°C and 30 MPa. In this condition, the yield of oil was 5.96% and the acid, peroxide, free fatty acid, and p-anisidine values were 4.49 mg KOH/g, 4.72 meq/kg, 3.42%, and 10.03, respectively. The ω-3 PUFAs content significantly increased in 2-MAG obtained from Novozymes 435, Lipozyme TLIM, and Lipozyme RMIM to 43.03 ± 0.36, 45.95 ± 0.29, and 40.50 ± 0.77%, respectively (p < 0.05). A thin layer chromatography (TLC) analysis confirmed the production and separation of 2-MAG in the ethanolysis process. The ratio of total ω-3 to ω-6 fatty acids was almost twice in 2-MAG of SC-CO₂ extracted oyster oil. SC-CO₂ extracted Pacific oyster oil can be used for sn-1,3 specific lipases catalyzed ethanolysis to produce ω-3 PUFAs rich in 2-MAG.     

Enzymatic activity of L-amino acid oxidase from snake venom Crotalus adamanteus in supercritical CO2

L-amino acid oxidase (L-AAO) from snake venom Crotalus adamanteus was successfully tested as a catalyst in supercritical CO₂ (SC-CO₂). The enzyme activity was measured before and after exposure to supercritical conditions (40°C, 110 bar). It was found that L-AAO activity slightly increased after SC-CO₂ exposure by up to 15%. L-AAO was more stable in supercritical CO₂ than in phosphate buffer under atmospheric pressure, as well as in the enzyme membrane reactor (EMR) experiment. 3,4-Dihydroxyphenyl-L-alanine (L-DOPA) oxidation was performed in a batch reactor made of stainless steel that could withstand the pressures of SC-CO₂, in which L-amino acid oxidase from C. adamanteus was able to catalyze the reaction of oxidative deamination of L-DOPA in SC-CO₂. For the comparison L-DOPA oxidation was performed in the EMR at 40°C and pressure of 2.5 bar. Productivity expressed as mmol-s of converted L-DOPA after 3?h per change of enzyme activity after 3?h was the highest in SC-CO₂ (1.474?mmol?U^?1), where catalase was present, and the lowest in the EMR (0.457?mmol?U^?1).     

Supercritical CO2 Induces Marked Changes in Membrane Phospholipids Composition in Escherichia coli K12

Supercritical carbon dioxide (SC-CO₂) treatment is one of the most promising alternative techniques for pasteurization of both liquid and solid food products. The inhibitory effect of SC-CO₂ on bacterial growth has been investigated in different species, but the precise mechanism of action remains unknown. Membrane permeabilization has been proposed to be the first event in SC-CO₂-mediated inactivation. Flow cytometry, high performance liquid chromatography–electrospray ionization–mass spectrometry and NMR analyses were performed to investigate the effect of SC-CO₂ treatment on membrane lipid profile and membrane permeability in Escherichia coli K12. After 15 min of SC-CO₂ treatment at 120 bar and 35 °C, the majority of bacterial cells dissipated their membrane potential (95 %) and lost membrane integrity, as 81 % become partially permeabilized and 18 % fully permeabilized. Membrane permeabilization was associated with a 20 % decrease in bacterial biovolume and to a strong (>50 %) reduction in phosphatidylglycerol (PG) membrane lipids, without altering the fatty acid composition and the degree of unsaturation of acyl chains. PGs are thought to play an important role in membrane stability, by reducing motion of phosphatidylethanolamine (PE) along the membrane bilayer, therefore promoting the formation of inter-lipid hydrogen bonds. In addition, the decrease in intracellular pH induced by SC-CO₂ likely alters the chemical properties of phospholipids and the PE/PG ratio. Biophysical effects of SC-CO₂ thus cause a strong perturbation of membrane architecture in E. coli, and such alterations are likely associated with its strong inactivation effect.     

Continuous Bioconversion of the Lipids of Corn,Wheat, and Triticale Distiller’s Dried Grains with Solubles to Biodiesel in Supercritical Carbon Dioxide and Characterization of the Products

Lipids of corn, wheat, and triticale distiller’s dried grains with solubles (DDGS) were extracted with supercritical carbon dioxide (SC-CO₂) and converted to biodiesel (fatty acid methyl esters; FAME) in a continuous SC-CO₂ bioreactor using immobilized lipase. Different properties of the products obtained were characterized. FAME content of the products ranged between 87.1 % (corn DDGS lipid biodiesel; CB) and 92.0 % (triticale DDGS lipid biodiesel; TB). CB had a higher viscosity (6.24 mm²/s) than those of wheat DDGS lipid biodiesel (WB) (5.97 mm²/s) and TB (5.67 mm²/s). Cloud point of CB, WB, and TB were ?8.48, ?6.52, and ?5.04 °C, respectively. Oxidative stability of WB and TB was higher than that of CB. Heat of combustion of products was 39.4–39.6 kJ/g. Continuous bioconversion of DDGS lipids to biodiesel in SC-CO₂ is a simple, efficient, and “green” alternative to the conventional process and targets new opportunities for the biodiesel industry.     

Geotrichum candidum 4013: Extracellular lipase versus cell-bound lipase from the single strain

Two types of lipases (extracellular and cell-bound) were produced by Geotrichum candidum 4013 in liquid medium and were used as biocatalysts in blackcurrant oil hydrolysis. Reaction products were analysed for the degree of conversion from which enzyme activity was evaluated, and the composition of free fatty acids was compared to the composition of oil substrate. The enzyme activity was measured also before and after the reaction in SC-CO₂. The fatty acid composition of the acids liberated from oil by hydrolysis suggests a specificity of the cell-bound and extracellular enzymes from Geotrichum candidum 4013. The extracellular lipase displays low selectivity to the polyunsaturated fatty acids, and the cell-bound lipase possesses selectivity to the saturated fatty acids. Enantioselectivity of the tested processes achieved with both induced enzymes was high (from 43 to 242). The activity of all enzymes has markedly increased after their exposure to SC-CO₂. The treatment of enzymes by SC-CO₂ could be easy-to-use approaches to improve the efficiency of enzymatic reactions.     

Supercritical carbon dioxide pretreatment of corn stover and switchgrass for lignocellulosic ethanol production

Supercritical CO₂ (SC-CO₂), a green solvent suitable for a mobile lignocellulosic biomass processor, was used to pretreat corn stover and switchgrass at various temperatures and pressures. The CO₂ pressure was released as quickly as possible by opening a quick release valve during the pretreatment. The biomass was hydrolyzed after pretreatment using cellulase combined with β-glucosidase. The hydrolysate was analyzed for the amount of glucose released. Glucose yields from corn stover samples pretreated with SC-CO₂ were higher than the untreated sample’s 12% glucose yield (12 g/100 g dry biomass) and the highest glucose yield of 30% was achieved with SC-CO₂ pretreatment at 3500 psi and 150 °C for 60 min. The pretreatment method showed very limited improvement (14% vs. 12%) in glucose yield for switchgrass. X-ray diffraction results indicated no change in crystallinity of the SC-CO₂ treated corn stover when compared to the untreated, while SEM images showed an increase in surface area.     

Optimisation of n-octyl oleate enzymatic synthesis over Rhizomucor miehei lipase

Octyl oleate is a useful organic compound with several applications in cosmetic, lubricant and pharmaceutical industry. At first, the enzymatic synthesis of n-octyl oleate by direct lipase-catalysed esterification of oleic acid and 1-octanol was investigated in a stirred batch reactor in solvent-free system. A systematic screening and optimisation of the reaction parameters were performed to gain insight into the kinetics mechanism. Particularly, enzyme concentration, reaction temperature, stirrer speed, water content, substrates concentration and molar ratio were optimised with respect to the final product concentration and reaction rate. The kinetics mechanism of the reaction was investigated. Finally, a comparison of the experimental results obtained in a solvent free-system with those using two different solvents, supercritical carbon dioxide (SC-CO₂) and n-hexane, was proposed. It resulted that in SC-CO₂ higher concentration of the desired product was attained, requiring lower enzyme concentrations to achieve comparable conversion of free fatty acid into fatty acid ester.     

Pretreatment of sugarcane bagasse using supercritical carbon dioxide combined with ultrasound to improve the enzymatic hydrolysis

This work evaluates the pretreatment of sugarcane bagasse combining supercritical carbon dioxide (SC-CO₂) and ultrasound to enhance the enzymatic hydrolysis of pretreated bagasse. In a first step the influence of process variables on the SC-CO₂ pretreatment to enhance the enzymatic hydrolysis was evaluated by mean of a Plackett–Burmann design. Then, the sequential treatment combining ultrasound + SC-CO₂ was evaluated. Results show that treatment using SC-CO₂ increased the amount of fermentable sugar obtained of about 280% compared with the non-treated bagasse, leading to a hydrolysis efficiency (based on the amount of cellulose) as high as 74.2%. Combining ultrasound + SC-CO₂ treatment increased about 16% the amount of fermentable sugar obtained by enzymatic hydrolysis in comparison with the treatment using only ultrasound. From the results presented in this work it can be concluded that the combined ultrasound + SC-CO₂ treatment is an efficient and promising alternative to carry out the pretreatment of lignocellulosic feedstock at relatively low temperatures without the use of hazardous solvents.     

Investigating the mechanism of the selective hydrogenation reaction of cinnamaldehyde catalyzed by Pt<Subscript>n</Subscript> clusters

Cinnamaldehyde (CAL) belongs to the group of aromatic α,β-unsaturated aldehydes; the selective hydrogenation of CAL plays an important role in the fine chemical and pharmaceutical industries. Using Pt_n clusters as catalytic models, we studied the selective hydrogenation reaction mechanism for CAL catalyzed by Pt_n (n?=?6, 10, 14, 18) clusters by means of B3LYP in density functional theory at the 6-31+?G(d) level (the LanL2DZ extra basis set was used for the Pt atom). The rationality of the transition state was proved by vibration frequency analysis and intrinsic reaction coordinate computation. Moreover, atoms in molecules theory and nature bond orbital theory were applied to discuss the interaction among orbitals and the bonding characteristics. The results indicate that three kinds of products, namely 3-phenylpropyl aldehyde, 3-phenyl allyl alcohol and cinnamyl alcohol, are produced in the selective hydrogenation reaction catalyzed by Pt_n clusters; each pathway possesses two reaction channels. Pt_n clusters are more likely to catalyze the activation and hydrogenation of the C?=?O bond in CAL molecules, eventually producing cinnamic alcohol, which proves that Pt_n clusters have a strong reaction selectivity to catalyze CAL. The reaction selectivity of the catalyzer cluster is closely related to the size of the Pt_n cluster, with Pt₁₄ clusters having the greatest reaction selectivity.

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Graphical Abstract The reaction mechanism for the selective hydrogenation reaction ofcinnamaldehyde catalyzed by Pt_n clusters was studied by densityfunctional theory. The reactionselectivity of cluster catalyzer was concluded to be closely related to the size of Pt_n clusters, with Pt₁₄ clusters having the greatest reaction selectivity

     

Trichloroacetic acid dehalogenation by reductive radicals

Advanced oxidation processes, using either UVC/H₂O₂ or UVC/K₂S₂O₈, both in the presence of H₂CO₂ or CH₃OH are very efficient in mineralizing aqueous solutions of trichloroacetic acid (TCAA) leaving no toxic residues. The main reaction initiating TCAA depletion is its reduction by the radicals or CH₂OH to yield radicals and Cl⁻ anions. Further thermal reactions of lead to the formation of CO₂ and HCl. Molecular oxygen competes with TCAA for and CH₂OH radicals. However, in experiments under continuous irradiation of initially air-saturated solutions in closed reactors, the dissolved molecular oxygen concentration was depleted to low enough levels to favor the reaction of the reducing radicals with TCAA. A general reaction mechanism is proposed and discussed. The reaction between superoxide radical anions and TCAA was found to be of low efficiency.     

Some factors that influence the nonenzymatic glycation of peptides and polypeptides by glyceraldehyde

The rate of reaction of glyceraldehyde with a series of peptides was found to be dependent on their amino acid composition, sequence, and chain length. The presence of a histidine near the NH₂-terminal increased the rate of glycation, whereas the presence of a carboxyl group near the reaction site led to a decrease in reaction rate. In general, tripeptides reacted faster than dipeptides, and dipeptides reacted faster than amino acids. Sodium phosphate and 2,3-diphosphoglycerate enhanced the rate of reaction of glyceraldehyde with all the dipeptides tested. Sodium chloride inhibited the reaction in phosphate buffer, but not in HEPES buffer. The NH₂-terminal heptapeptide from the -chain of human hemoglobin A (HbA), where histidine is the second residue, reacted with glyceraldehyde faster than the NH₂-terminal hexapeptide from the -chain. The glycation of tetrameric human Hb by glyceraldehyde was found to be dependent on the ligation state of the protein since deoxy-HbA reacted about 50% more with glyceraldehyde than did liganded HbA. The enhanced glycation of deoxy HbA was mainly attributable to the more extensive reaction at the NH₂-terminal of the -chain. The presence of a histidine adjacent to the NH₂-terminal at this site may facilitate the Amadori rearrangement. The glycation of horse Hb in which the second residue is glutamine was not increased under anaerobic conditions.     

Mercury(II)-methylene blue interactions: Complexation and metallate formation

Reactions of HgX₂ (X = Cl, Br, I) with methylene blue (MB) chloride dihydrate and the reaction of HgCl₂ with MB nitrate dihydrate have been undertaken in an attempt to prepare metal derivatives of MB. The products were characterized by elemental analysis, UV-Vis, IR, ¹H NMR spectroscopy and X-ray crystallography. The reaction of HgCl₂ with MB chloride dihydrate and subsequent crystallization in a DMF/H₂O mixture yielded the products (1 and 2) with different crystal morphologies. The structure of complex 1 represents the first structural report of a complex of MB with any metal ion. The efficacy of MB to act as a ligand in spite of its cationic nature is thus demonstrated. The structure of 1 comprises a distorted tetrahedral geometry around Hg(II); the coordination valencies being provided by three chloride ions and a MB cation. The structure of 2 is a salt consisting of an anion and two MB cations. The reaction of HgI₂ and HgBr₂ with MB chloride dihydrate yielded salts 3 and 4 with (X = Br or I) anions and MB cations. A mixed salt 5, whose anions comprise mercury(II), chloride and nitrate species resulted from the reaction between HgCl₂ with MB nitrate dihydrate. The reaction of Hg₂F₂ with MB chloride dihydrate and the crystallization of the resulting product 6 in aqueous DMF yielded crystals of (MB)₂HgCl₄ · H₂O.     

Pilot-scale supercritical carbon dioxide extractions for the recovery of triacylglycerols from microalgae: a practical tool for algal biofuels research

We describe the preliminary extractions from a pilot-scale supercritical carbon dioxide (SC-CO₂) extractor for the isolation of algal lipids suitable for small-scale conversion to liquid hydrocarbon fuels. Flowable oils were recovered from SC-CO₂ extractions of lyophilized Nannochloropsis granulata. The extracted oils were determined to be composed primarily of triacylglycerols (TAG) by liquid chromatography–mass spectrometry analysis. Gravimetric lipid yield was increased significantly from 15.56 to 28.45 mg g^?1 ash-free dry weight (AFDW) with an increase in temperature from 50°C to 70°C, at 35 MPa over 270 min. Varying pressure had no significant effect on lipid yield. Liquid chromatography–mass spectrometry analysis of the SC-SO₂ extracts indicated that the TAG profile remained constant regardless of extraction pressure, and analysis of fatty acid methyl esters (FAME) revealed a uniform profile throughout all extraction conditions. Our optimized gravimetric lipid yields from N. granulata (28.45 mg g^?1 AFDW) were approximately half of the yields obtained by Soxhlet extraction with hexane (57.53 mg g^?1 AFDW); however, the FAME yields were similar regardless of extraction technique (18.23 mg FAME g^?1 and 17.35 mg FAME g^?1 AFDW from SC-CO₂ extraction and hexane extraction, respectively). Further extractions with Botryococcus braunii indicated that fatty acid extraction by SC-CO₂ was as efficient as hexane extraction. These results highlight the suitability of SC-CO₂ for large-scale oil extraction of microalgae for biofuel or biojet analyses due to its selectivity for TAG extraction.     

Identification of anti-lung cancer extract from Chlorella vulgaris C-C by antioxidant property using supercritical carbon dioxide extraction

In this study, supercritical carbon dioxide extraction (SC-CO₂) technology was developed to extract the active components (such as antioxidants) from a novel microalga, Chlorella vulgaris C-C, due to its superior advantages over conventional solvent or ultrasonic extraction methods. Using SC-CO₂ and ultrasonic extractions, the polyphenol contents of C. vulgaris C-C were 13.40 and 0.46 (mg_{gallic acid}/g lyophilized extract), respectively. The flavonoid content obtained from SC-CO₂ (3.18 mg_quercetin/g lyophilized extract) was also significantly higher than from ultrasonic extraction (0.86 mg_quercetin/g lyophilized extract). Investigation of C. vulgaris C-C extract from SC-CO₂ indicates strong antioxidant activities in radical scavenging, ferric reducing power and metal chelating abilities. In cell proliferation assay, the extract of C. vulgaris C-C inhibits human lung cancer H1299, A549, and H1437 cells in a dose-dependent manner. In addition, the treatment with extracts of C. vulgaris C-C effectively reduced the migration of tumor cells, suggesting the potential of using the C. vulgaris C-C extract to inhibit lung cancer metastasis.     

Impact of extraction conditions on bergapten content and antimicrobial activity of oils obtained by a co-extraction of citrus by-products using supercritical carbon dioxide

Citrus oils obtained from citrus by-products are widely used in many areas because of their bioactive nature. However, their use in products has been restricted due to phototoxicity and other health problems of some of the non-volatile compounds, especially bergapten. We studied the effect of supercritical carbon dioxide (SC-CO₂) extraction conditions on the minimization of bergapten content for the oils obtained from a combination of citrus peels and seeds. The influence of combined citrus by-products on cytotoxicity, antimicrobial activity, and other quality characteristics was studied so that those by-products can be used effectively. A second-order polynomial model showed a suitable fitting of the experimental value for the bergapten content (R² = 0.977, p < 0.05). Optimization (minimization of bergapten content) and validation were performed. The optimum conditions were 200.54 bar, 46.28°C and 34.98 g/min for pressure, temperature, and flow rate, respectively. The corresponding predicted value was 37.82 μg/g oil, which agreed well with the experimental value (38.36 ± 0.44 μg/g oil), affirming the adequacy and validity of the predicted model. The oil displayed higher antimicrobial activity and was less susceptible to fungi than bacteria. The cytotoxicity of the oil on HaCaT cells was low (84.59 ± 1.24% cell viability) for a concentration of 500 μg/mL. SC-CO₂ extraction of a mixture of citrus by-products can yield oils with low bergapten content, low toxicity, and higher antimicrobial activity, which could have a variety of applications.     

Inactivation of Alternaria brassicicola spores by supercritical carbon dioxide with ethanol entrainer

Supercritical carbon dioxide (SC-CO₂) was used to inactivate fungal spores of Alternaria brassicicola. The inactivation conditions were optimized using response surface methodology (RSM). When the SC-CO₂-entrainer (ethanol) system was applied to fungal spores, the treatment time required for the complete inactivation of fungal spores was substantially reduced.     

Catalysis of the acetylene hydrochlorination reaction by Si-doped Au clusters: a DFT study

The mechanisms for the acetylene hydrochlorination reaction on pristine Au₇ and Au₈ clusters and on the Si-doped Au clusters Au₆Si and Au₇Si were systematically investigated via density functional theory using the PBE functional. The band gap (?E_g) of the Au₇Si cluster was found to smaller than that of its undoped equivalent (Au₈), thus enhancing its catalytic activity, and Au₇Si presented a significantly reduced activation barrier (16.69 kcal mol^?1) for the acetylene hydrochlorination reaction compared with the pristine Au₈ cluster (21.83 kcal mol^?1). On the other hand, the activation barrier for the acetylene hydrochlorination reaction was not lower for the Au₆Si cluster than for the pristine Au₇ cluster because the band gap (?E_g) of Au₆Si was found to be larger than that of Au₇. Hence, the current work shows that the catalytic activities of gold clusters can be systematically modified by doping them. Our findings also suggest how to enhance the acetylene hydrochlorination reaction by doping foreign atoms into Au clusters.

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Graphical abstract The Si-doped Au₇Si cluster showed stronger catalytic activity for the acetylene hydrochlorination reaction compared with the pristine Au₈ cluster.

     

Effect of moisture on enzymatic reaction in supercritical carbon dioxide

The continuous acidolysis of triolein and stearic acid was carried out by an immobilized lipase to elucidate the characteristics of supercritical carbon dioxide (SC-CO₂) as a reaction medium. At first, an effect of temperature and pressure on the water adsorption to the immobilized lipase in the SC-CO₂ was examined. Then, the continuous interesterification of triolein and stearic acid by the moist immobilized lipase was examined. The amount of water adsorption to the immobilized lipase in the supercritical carbon dioxide measured under the condition of a different temperature and pressure has been expressed by a correlation equation of Freundlich type by using relative water standardized with the solubility of water in each condition. Optimum operating conditions of the interesterification by immobilized lipase in the SC-CO₂ was 323 K, 16.9 MPa and adsorbed-water concentration of 2 wt%. The production rate obtained by enzymatic acidolysis in the SC-CO₂ was found to be about 0.03 mmol/h2g-immobilized enzyme, leaving 74% residual triglyceride at the optimum operating conditions.     

Molecular assembly of CuBrSe3 in ethylene glycol solvent

CuBrSe₃ has been synthesized by the reaction between CuBr₂ and Se in ethylene glycol (EG) solvent at 100 °C. In the process, CuBr₂ was reduced to brom-complexes of Cu(I), such as , the complexes participated in the reaction as intermediates. Based on experimental results and the structure characterization of CuBrSe₃ crystal, a possible mechanism for CuBrSe₃ formation was proposed. The mechanism suggests that Se chains assembly with the brom-complexes of Cu(I) to form CuBr helical chains, and then CuBrSe₃ crystal.     

Studies on ventilation of culture broths. I. Behavior of CO2 in model systems

The rate of dissolution and dehydration of CO₂ in a liquid model system was investigated. Components in the model system established the main conditions which may exist, in the extracellular space of a microbiological culture liquid. The charge in voltage of a glass electrode was measured which indicated the formation of H⁺ ions in the H₂CO₃ ? HCO H⁺ reaction. The rate of CO₂ hydration increased with the increase of temperature from 0 to 40°C. Likewise the equilibrium of the reaction was shifted towards the forward reaction. Similar results were observed when the tip velocity of the impeller was increased. Data suggest that agitation promotes the dissolution of CO₂ in the culture liquid through the reduction of gas-liquid film resistance in the diffusion of this gas. The rate of hydration of CO₂ into the bulk of the liquid was independent of pCO₂ above the surface of the liquid but depended on pCO₂ in the gas bubble within the liquid. The concentration of HCO was, furthermore, influenced by the buffer components, buffer capacity, and the viscosity of the system. Since pCO₂ and the HCO concentration in the extracellular space depend on both physical and chemical factors, the ventilation of a culture liquid necessitates both exhaust of CO₂ from the gas bubbles of the culture broth and shift of the H₂CO₃ ? HCO + H⁺ reaction towards the backward direction.