ABSTRACT
The acylation of flavonoids serves as a means to alter their physicochemical properties, enhance their stability, and improve their bioactivity. Compared with natural flavonoid glycosides, the acylation of nonglycosylated flavonoids presents greater challenges since they contain fewer reactive sites. In this work, we propose an efficient strategy to solve this problem based on a first α-glucosylation step catalyzed by a sucrose phosphorylase, followed by acylation using a lipase. The method was applied to phloretin, a bioactive dihydrochalcone mainly present in apples. Phloretin underwent initial glucosylation at the 4'-OH position, followed by subsequent (and quantitative) acylation with C8, C12, and C16 acyl chains employing an immobilized lipase from Thermomyces lanuginosus. Electrospray ionization-mass spectrometry (ESI-MS) and two-dimensional nuclear magnetic resonance spectroscopy (2D-NMR) confirmed that the acylation took place at 6-OH of glucose. The water solubility of C8 acyl glucoside closely resembled that of aglycone, but for C12 and C16 derivatives, it was approximately 3 times lower. Compared with phloretin, the radical scavenging capacity of the new derivatives slightly decreased with 2,2-diphenyl-1-picrylhydrazyl (DPPH) and was similar to 2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTSâ¢+). Interestingly, C12 acyl-α-glucoside displayed an enhanced (3-fold) transdermal absorption (using pig skin biopsies) compared to phloretin and its α-glucoside.
Subject(s)
Flavonoids , Malus , Animals , Swine , Flavonoids/chemistry , Phloretin , Malus/chemistry , Glucosides , Acylation , Lipase/chemistry , AntioxidantsABSTRACT
BACKGROUND: Milk whey, a byproduct of the dairy industry has a negative environmental impact, can be used as a raw material for added-value compounds such as galactooligosaccharides (GOS) synthesis by bgalactosidases. RESULTS: B-gal42 from Pantoea anthophila strain isolated from tejuino belonging to the glycosyl hydrolase family GH42, was overexpressed in Escherichia coli and used for GOS synthesis from lactose or milk whey. Crude cell-free enzyme extracts exhibited high stability; they were employed for GOS synthesis reactions. In reactions with 400 g/L lactose, the maximum GOS yield was 40% (w/w) measured by HPAEC-PAD, corresponding to 86% of conversion. This enzyme had a strong predilection to form GOS with b(1 ? 6) and b (1 ? 3) galactosyl linkages. Comparing GOS synthesis between milk whey and pure lactose, both of them at 300 g/L, these two substrates gave rise to a yield of 38% (60% of lactose conversion) with the same product profile determined by HPAEC-PAD. CONCLUSIONS: B-gal42 can be used on whey (a cheap lactose source) to produce added value products such as galactooligosaccharides.
Subject(s)
Oligosaccharides/biosynthesis , beta-Galactosidase/metabolism , Pantoea , Lactose/metabolism , Recombinant Proteins , Dairying , WheyABSTRACT
The transglycosylation activity of a novel commercial ß-galactosidase from Bifidobacterium bifidum (Saphera) was evaluated. The optimal conditions for the operation of this enzyme, measured with o-nitrophenyl-ß-d-galactopyranoside, were 40 °C and pH around 6.0. Although at low lactose concentrations the property of this enzyme was basically hydrolytic, an increase of lactose concentration to 400 g/L resulted in a significant formation (107.2 g/L, 27% yield) of prebiotic galactooligosaccharides (GOS). The maximum amount of GOS was obtained at a lactose conversion of approximately 90%, which contrasts with other ß-galactosidases, for which the highest GOS yield is achieved at 40-50% lactose conversion. Using high-performance anion-exchange chromatography with pulsed amperometric detection, semipreparative high-performance liquid chromatography-hydrophilic interaction liquid chromatography, mass spectrometry, and 1D and 2D NMR, we determined the structure of most of the GOS synthesized by this enzyme. The main identified products were Gal-ß(1â3)-Gal-ß(1â4)-Glc (3'-O-ß-galactosyl-lactose), Gal-ß(1â6)-Glc (allolactose), Gal-ß(1â3)-Glc (3-galactosyl-glucose), Gal-ß(1â3)-Gal (3-galactobiose), and the tetrasaccharide Gal-ß(1â3)-Gal-ß(1â3)-Gal-ß(1â4)-Glc. In general, B. bifidum ß-galactosidase showed a tendency to form ß(1â3) linkages followed by ß(1â6) and more scarcely ß(1â4).
Subject(s)
Bacterial Proteins/metabolism , Bifidobacterium bifidum/enzymology , Oligosaccharides/biosynthesis , beta-Galactosidase/metabolism , Bacterial Proteins/genetics , Bifidobacterium bifidum/chemistry , Bifidobacterium bifidum/genetics , Carbohydrate Conformation , Chromatography, High Pressure Liquid , Galactose/metabolism , Lactose/metabolism , Mass Spectrometry , Oligosaccharides/chemistry , beta-Galactosidase/geneticsABSTRACT
The glucose isomerase GICA from Caldicoprobacter algeriensis was immobilized by ionic adsorption on polymethacrylate carriers (Sepabeads EC-EA and EC-HA) or covalent attachment to glyoxal agarose. The Sepabeads EC-HA yielded the highest recovery of activity (89%). The optimum temperature and pH of immobilized GICA were 90⯰C and 7.0, respectively, similar to the corresponding values of free enzyme. Nevertheless, the adsorbed enzyme displayed higher relative activity at acidic pH, greater thermostability, and better storage stability, compared to the free form. Moreover, the immobilized enzyme showed an excellent operational stability, in 15 successive 3â¯h reaction cycles at 85⯰C under a batch reactor, preserving 83% of its initial activity. Interestingly, a continuous process for High Fructose Syrup (HFS) production was established with the adsorbed GICA using a packed bed reactor during eleven days at 70⯰C. HPAEC-PAD analysis showed a maximum bioconversion rate of 49% after 48â¯h of operation.
Subject(s)
Aldose-Ketose Isomerases/metabolism , Batch Cell Culture Techniques/methods , Clostridiales/enzymology , Fructose/metabolism , Aldose-Ketose Isomerases/chemistry , Enzyme Stability , Enzymes, Immobilized/chemistry , Enzymes, Immobilized/metabolism , Hydrogen-Ion Concentration , Sepharose/chemistry , TemperatureABSTRACT
Enzymatic glycosylation of polyphenols is a tool to improve their physicochemical properties and bioavailability. On the other hand, glycosidic enzymes can be inhibited by phenolic compounds. In this work, we studied the specificity of various phenolics (hydroquinone, hydroxytyrosol, epigallocatechin gallate, catechol and p-nitrophenol) as fructosyl acceptors or inhibitors of the ß-fructofuranosidase from Xanthophyllomyces dendrorhous (pXd-INV). Only hydroquinone and hydroxytyrosol gave rise to the formation of glycosylated products. For the rest, an inhibitory effect on both the hydrolytic (H) and transglycosylation (T) activity of pXd-INV, as well as an increase in the H/T ratio, was observed. To disclose the binding mode of each compound and elucidate the molecular features determining its acceptor or inhibitor behaviour, ternary complexes of the inactive mutant pXd-INV-D80A with fructose and the different polyphenols were analyzed by X-ray crystallography. All the compounds bind by stacking against Trp105 and locate one of their phenolic hydroxyls making a polar linkage to the fructose O2 at 3.6-3.8 Å from the C2, which could enable the ulterior nucleophilic attack leading to transfructosylation. Binding of hydroquinone was further investigated by soaking in absence of fructose, showing a flexible site that likely allows productive motion of the intermediates. Therefore, the acceptor capacity of the different polyphenols seems mediated by their ability to make flexible polar links with the protein, this flexibility being essential for the transfructosylation reaction to proceed. Finally, the binding affinity of the phenolic compounds was explained based on the two sites previously reported for pXd-INV.
Subject(s)
Basidiomycota/enzymology , Fungal Proteins/antagonists & inhibitors , Phenols/pharmacology , beta-Fructofuranosidase/antagonists & inhibitors , Basidiomycota/genetics , Catalytic Domain , Chromatography, High Pressure Liquid , Chromatography, Thin Layer , Crystallography, X-Ray , Fructose/metabolism , Fungal Proteins/genetics , Fungal Proteins/metabolism , Glycosylation , Hydrolysis , Models, Molecular , Molecular Structure , Polyphenols/metabolism , Recombinant Fusion Proteins/metabolism , Spectrometry, Mass, Electrospray Ionization , Structure-Activity Relationship , Substrate Specificity , beta-Fructofuranosidase/genetics , beta-Fructofuranosidase/metabolismABSTRACT
(-)-Epigallocatechin gallate (EGCG), the predominant catechin (≥50%) in green tea (Camellia sinensis), displays several bioactive properties but its stability and bioavailability are low. In this work, the properties of two α-glucosyl derivatives of EGCG (3'- and 7-O-α-D-glucopyranoside), obtained by enzymatic synthesis, were assessed. The α-glucosylation enhanced the pH and thermal stability of EGCG. The analysis of scavenging activity toward ABTS·+ radicals showed that the α-glucosylation at C-7 of A-ring caused a higher loss of antioxidant activity compared with the sugar conjugation at C-3' of B-ring. The 3'-glucoside also showed higher potential to alleviate intracellular reactive oxygen species (ROS) levels and to boost REDOX activity. The toxicity of EGCG and its monoglucosides was tested in human SH-S5Y5 neurons, RAW 264.7 macrophages, MRC5 fibroblasts, and HT-29 colon cancer cells. Interestingly, the 3'-O-α-D-glucoside increased the viability of neural cells in vitro (2.75-fold at 100 µM) in the presence of H2O2, whilst EGCG gave rise only to a 1.7-fold enhancement. In conclusion, the α-glucoside of EGCG at C-3' has a great potential for nutraceutical, cosmetic and biomedical applications.
ABSTRACT
The regioselective α-glucosylation of hesperetin was achieved by a transglycosylation reaction catalyzed by cyclodextrin glucanotransferase (CGTase) from Thermoanaerobacter sp. using soluble starch as glucosyl donor. By combining mass spectrometry (ESI-TOF) and 2D-NMR analysis, the main monoglucosylated derivative was fully characterized (hesperetin 7-O-α-d-glucopyranoside). In order to increase the yield of monoglucoside, several reaction parameters were optimized: Nature and percentage of cosolvent, composition of the aqueous phase, glucosyl donor, temperature, and the concentrations of hesperetin and soluble starch. Under the optimal conditions, which included the presence of 30% of bis(2-methoxyethyl) ether as cosolvent, the maximum concentration of monoglucoside was approximately 2 mM, obtained after 24 h of reaction. To our knowledge, this is the first report of direct glucosylation of hesperetin employing free enzymes instead of whole cells.
Subject(s)
Glucosyltransferases/chemistry , Hesperidin/chemistry , Catalysis , Chromatography, High Pressure Liquid , Glucosyltransferases/metabolism , Glycosylation , Hesperidin/metabolism , Mass Spectrometry , Molecular StructureABSTRACT
Carbohydrate fatty acid esters have a broad spectrum of applications in the food, cosmetic, and pharmaceutical industries. The enzyme-catalyzed acylation is significantly more selective than the chemical process and is carried out at milder conditions. Compared with mono- and disaccharides, the acylation of trisaccharides has been less studied. However, trisaccharide esters display notable bioactive properties, probably due to the higher hydrophilicity of the sugar head group. In this chapter, we describe the acylation of two trisaccharides, maltotriose and 1-kestose, catalyzed by different immobilized lipases, using vinyl esters as acyl donors. To illustrate the potential of such compounds, the antitumor activity of 6â³-O-palmitoyl-maltotriose is shown.
Subject(s)
Esters/metabolism , Fatty Acids/metabolism , Lipase/metabolism , Trisaccharides/metabolism , Acylation , Catalysis , Cell Line , Chromatography, High Pressure Liquid , Esters/chemistry , Fatty Acids/chemistry , Humans , Mass Spectrometry , Trisaccharides/chemistryABSTRACT
The glycosylation of plant polyphenols may modulate their solubility and bioavailability and protect these molecules from oxygen, light degradation, and during gastrointestinal transit. In this work, the synthesis of various α-glucosyl derivatives of (-)-epigallocatechin gallate, the predominant catechin in green tea, was performed in water at 50 °C by a transglycosylation reaction catalyzed by cyclodextrin glycosyltransferase from Thermoanaerobacter sp. The molecular weight of reaction products was determined by high-performance liquid chromatography coupled to mass spectrometry. Using hydrolyzed potato starch as a glucosyl donor, two main monoglucosides were obtained with conversion yields of 58 and 13%, respectively. The products were isolated and chemically characterized by combining two-dimensional nuclear magnetic resonance methods. The major derivative was epigallocatechin gallate 3'- O-α-d-glucopyranoside (1), and the minor derivative was epigallocatechin gallate 7- O-α-d-glucopyranoside (2).
Subject(s)
Bacterial Proteins/chemistry , Catechin/analogs & derivatives , Glucosyltransferases/chemistry , Thermoanaerobacter/enzymology , Biocatalysis , Catechin/chemistry , Chromatography, High Pressure Liquid , Glycosylation , Mass SpectrometryABSTRACT
The synthesis of a novel α-glucosylated derivative of pterostilbene was performed by a transglycosylation reaction using starch as glucosyl donor, catalyzed by cyclodextrin glucanotransferase (CGTase) from Thermoanaerobacter sp. The reaction was carried out in a buffer containing 20% (v/v) DMSO to enhance the solubility of pterostilbene. Due to the formation of several polyglucosylated products with CGTase, the yield of monoglucoside was increased by the treatment with a recombinant amyloglucosidase (STA1) from Saccharomyces cerevisiae (var. diastaticus). This enzyme was not able to hydrolyze the linkage between the glucose and pterostilbene. The monoglucoside was isolated and characterized by combining ESI-MS and 2D-NMR methods. Pterostilbene α-d-glucopyranoside is a novel compound. The α-glucosylation of pterostilbene enhanced its solubility in water to approximately 0.1 g/L. The α-glucosylation caused a slight loss of antioxidant activity towards ABTSË⺠radicals. Pterostilbene α-d-glucopyranoside was less toxic than pterostilbene for human SH-S5Y5 neurons, MRC5 fibroblasts and HT-29 colon cancer cells, and similar for RAW 264.7 macrophages.
Subject(s)
Antineoplastic Agents/chemical synthesis , Antioxidants/chemical synthesis , Bacterial Proteins/chemistry , Glucan 1,4-alpha-Glucosidase/chemistry , Glucosides/chemical synthesis , Glucosyltransferases/chemistry , Stilbenes/chemistry , Animals , Antineoplastic Agents/pharmacology , Antioxidants/pharmacology , Bacterial Proteins/isolation & purification , Biocatalysis , Cell Line, Tumor , Cell Survival/drug effects , Fibroblasts/drug effects , Fibroblasts/metabolism , Fibroblasts/pathology , Glucan 1,4-alpha-Glucosidase/biosynthesis , Glucosides/pharmacology , Glucosyltransferases/biosynthesis , Glycosylation , HT29 Cells , Humans , Inhibitory Concentration 50 , Mice , Neurons/drug effects , Neurons/metabolism , Neurons/pathology , RAW 264.7 Cells , Recombinant Proteins/biosynthesis , Recombinant Proteins/chemistry , Saccharomyces cerevisiae/chemistry , Saccharomyces cerevisiae/enzymology , Solubility , Starch/chemistry , Thermoanaerobacter/chemistry , Thermoanaerobacter/enzymologyABSTRACT
OBJECTIVE: A simple and inexpensive methodology, based on the use of micro-centrifuge filter tubes, is proposed for establishing the best enzyme immobilization conditions. RESULTS: The immobilized biocatalyst is located inside the filter holder during the whole protocol, thus facilitating the incubations, filtrations and washings. This procedure minimizes the amount of enzyme and solid carrier needed, and allows exploring different immobilization parameters (pH, buffer concentration, enzyme/carrier ratio, incubation time, etc.) in a fast manner. The handling of immobilized enzymes using micro-centrifuge filter tubes can also be applied to assess the apparent activity of the biocatalysts, as well as their reuse in successive batch reaction cycles. The usefulness of the proposed methodology is shown by the determination of the optimum pH for the immobilization of an inulinase (Fructozyme L) on two anion-exchange polymethacrylate resins (Sepabeads EC-EA and Sepabeads EC-HA). CONCLUSION: The micro-scale procedure described here will help to overcome the lack of guidelines that usually govern the selection of an immobilization method, thus favouring the development of stable and robust immobilized enzymes that can withstand harsh operating conditions in industry.
Subject(s)
Enzymes, Immobilized/metabolism , Mass Screening/methods , Glycoside Hydrolases/metabolism , Hydrogen-Ion Concentration , Polymethacrylic Acids , Protein BindingABSTRACT
The formation of galactooligosaccharides (GOS) in skim milk during treatment with several commercial ß-galactosidases (Bacillus circulans, Kluyveromyces lactis and Aspergillus oryzae) was analysed in detail, at 4 and 40°C. The maximum GOS concentration was obtained at a lactose conversion of approximately 40-50% with B. circulans and A. oryzae ß-galactosidases, and at 95% lactose depletion for K. lactis ß-galactosidase. Using an enzyme dosage of 0.1% (v/v), the maximum GOS concentration with K. lactis ß-galactosidase was achieved in 1 and 5h at 40 and 4 °C, respectively. With this enzyme, it was possible to obtain a treated milk with 7.0 g/L GOS - the human milk oligosaccharides (HMOs) concentration is between 5 and 15 g/L--and with a low content of residual lactose (2.1g/L, compared with 44-46 g/L in the initial milk sample). The major GOS synthesised by this enzyme were 6-galactobiose [Gal-ß(1 â 6)-Gal], allolactose [Gal-ß(1 â 6)-Glc] and 6'-O-ß-galactosyl-lactose [Gal-ß(1 â 6)-Gal-ß(1 â 4)-Glc].
Subject(s)
Galactose/chemistry , Lactose/chemistry , Milk/chemistry , Oligosaccharides/chemistry , Prebiotics , Animals , Cattle , Humans , Kluyveromyces/enzymology , Milk/metabolism , Milk, Human/chemistry , beta-Galactosidase/chemistryABSTRACT
Unnatural selection: A fungal laccase was tailored by directed evolution to be active at neutral/alkaline pH. After five generations, the final mutant showed a broader pH profile while retaining 50 to 80 % of its activity at neutral pH.
Subject(s)
Directed Molecular Evolution , Laccase/genetics , Laccase/metabolism , Saccharomyces cerevisiae/enzymology , Hydrogen-Ion Concentration , Models, Molecular , Mutation , Saccharomyces cerevisiae/genetics , Substrate SpecificityABSTRACT
The in vitro fermentation of several purified galacto-oligosaccharides (GOS), specifically the trisaccharides 4'-galactosyl-lactose and 6'-galactosyl-lactose and a mixture of the disaccharides 6-galactobiose and allolactose, was carried out. The bifidogenic effect of GOS at 1% (w/v) was studied in a pH-controlled batch culture fermentation system inoculated with healthy adult human faeces. Results were compared with those obtained with a commercial GOS mixture (Bimuno-GOS). Changes in bacterial populations measured through fluorescence in situ hybridization and short-chain fatty acid (SCFA) production were determined. Bifidobacteria increased after 10-h fermentation for all the GOS substrates, but the changes were only statistically significant (P<0.05) for the mixture of disaccharides and Bimuno-GOS. Acetic acid, whose formation is consistent with bifidobacteria metabolism, was the major SCFA synthesized. The acetate concentration at 10 h was similar with all the substrates (45-50 mM) and significantly higher than the observed for formic, propionic and butyric acids. All the purified GOS could be considered bifidogenic under the assayed conditions, displaying a selectivity index in the range 2.1-3.0, which was slightly lower than the determined for the commercial mixture Bimuno-GOS.
Subject(s)
Bacteria/metabolism , Feces/microbiology , Trisaccharides/metabolism , Bacteria/genetics , Biota , Fatty Acids, Volatile/analysis , Fermentation , Humans , In Situ Hybridization, FluorescenceABSTRACT
The synthesis of galactooligosaccharides (GOS) catalyzed by ß-galactosidase from Aspergillus oryzae (Enzeco) was studied. Using 400 g/L of lactose and 15 U/mL, maximum GOS yield, measured by HPAEC-PAD, was 26.8% w/w of total carbohydrates, obtained at approximately 70% lactose conversion. No less than 17 carbohydrates were identified; the major transgalactosylation product was 6'-O-ß-galactosyl-lactose, representing nearly one-third (in weight) of total GOS. In contrast with previous reports, the presence of at least five disaccharides was detected, which accounted for 40% of the total GOS at the point of maximum GOS concentration (allolactose and 6-galactobiose were the major products). A. oryzae ß-galactosidase showed a preference to form ß(1â6) bonds, followed by ß(1â3) and ß(1â4) linkages. Results were compared with those obtained with ß-galactosidases from Kluyveromyces lactis and Bacillus circulans. The highest GOS yield and specific productivity were achieved with B. circulans ß-galactosidase. The specificity of the linkages formed and distribution of di-, tri-, and higher GOS varied significantly among the three ß-galactosidases.
Subject(s)
Aspergillus oryzae/enzymology , Trisaccharides/biosynthesis , beta-Galactosidase/metabolism , Bacillus/enzymology , Disaccharides/biosynthesis , Hydrogen-Ion Concentration , Kluyveromyces/enzymology , Lactose/biosynthesis , Magnetic Resonance Spectroscopy , TemperatureABSTRACT
The synthesis of galacto-oligosaccharides (GOS) catalyzed by a novel commercial preparation of ß-galactosidase from Bacillus circulans (Biolactase) was studied, and the products were characterized by MS and NMR. Using 400 g/L lactose and 1.5 enzyme units per milliliter, the maximum GOS yield, measured by HPAEC-PAD analysis, was 165 g/L (41% w/w of total carbohydrates in the mixture). The major transgalactosylation products were the trisaccharide Gal-ß(1â4)-Gal-ß(1â4)-Glc and the tetrasaccharide Gal-ß(1â4)-Gal-ß(1â4)-Gal-ß(1â4)-Glc. The GOS yield increased to 198 g/L (49.4% w/w of total carbohydrates) using a higher enzyme concentration (15 U/mL), which minimized the enzyme inactivation under reaction conditions. Using skim milk (with a lactose concentration of 46 g/L), the enzyme also displayed transgalactosylation activity: maximum GOS yield accounted for 15.4% (7.1 g/L), which was obtained at 50% lactose conversion.
Subject(s)
Bacillus/enzymology , Fungal Proteins/chemistry , Lactose/chemistry , Milk/chemistry , Oligosaccharides/chemical synthesis , beta-Galactosidase/chemistry , Animals , Carbohydrate Sequence , Cattle , Enzyme Stability , Kinetics , Molecular Sequence Data , Oligosaccharides/chemistry , TemperatureABSTRACT
Thermostable laccases with a high-redox potential have been engineered through a strategy that combines directed evolution with rational approaches. The original laccase signal sequence was replaced by the α-factor prepro-leader, and the corresponding fusion gene was targeted for joint laboratory evolution with the aim of improving kinetics and secretion by Saccharomyces cerevisiae, while retaining high thermostability. After eight rounds of molecular evolution, the total laccase activity was enhanced 34,000-fold culminating in the OB-1 mutant as the last variant of the evolution process, a highly active and stable enzyme in terms of temperature, pH range, and organic cosolvents. Mutations in the hydrophobic core of the evolved α-factor prepro-leader enhanced functional expression, whereas some mutations in the mature protein improved its catalytic capacities by altering the interactions with the surrounding residues.