Patent Application
20140072544
This invention relates to the area of biotechnology and in particular to probiotic strains of lactic acid bacteria and the polybacterial preparation, which is obtained by them. This invention also relates to the complex beneficial health effects of the preparation and its use as a dietary supplement for prevention of various diseases.
Probiotics are live edible microorganisms that have a positive effect on human health. Most probiotics are lactobacilli and/or bifidobacteria. They are non-pathogenic bacteria able to colonize on the gastrointestinal tract. It has been shown that lactobacilli and bifidobacteria are the major components of human microflora (microbiota). Representatives of both genuses can colonize the mucosa layer of the colon and affect homeostasis maintenance of the intestinal ecosystem. Their presence is associated with beneficial health effects such as suppression of harmful microorganisms, improvement of digestion, immune stimulating effect, reduction of lactose intolerance, reduction of serum cholesterol, prevention of diarrhea and others. Some strains of lactobacilli produce bioactive peptides that have antihypertensive effect as well as calcium- and magnesium-absorbing effect. In general, probiotic effects do not relate to the genus Lactobacillus and Bifidobacterium, but are strain specific. In order to prove beneficial effects an accurate identification of species and strains is carried out during studying. Many beneficial health effects are registered after the consumption of products containing probiotic strains. Below are listed the most important benefits:
Several strains of lactic acid bacteria produce bacteriocins, which destroy harmful microorganisms such as Clostridium tyrobutiricum, St. aureus, Listeria monocytogenes and others.
In a healthy human body are produced about 400 mM short-chain fatty acids per day, as the most important are: acetic acid, propionic acid and butyric acid. They favorably affect the pH in the intestine. It was found that butyrate reduces the risk of developing colon cancer by inhibiting the genotoxic effect of nitrosamines and hydrogen peroxide. Furthermore, butyric acid induces apoptosis in tumor cells of the colon. Fatty acid reduces the expression of proinflammatory cytokines TNFα, IL-1β, IL-6.
Probiotic bacteria regulate the delicate balance between necessary and excessive immune response. Probiotic strains that lead to stimulation of the induction of IL-10 are suitable for people suffering from inflammatory disease of the colon. Immunomodulating effect is strain specific. Several strains of lactobacilli and bifidobacteria, some of which lead to reduction of TNFα and increase of IL-10 (McCarthy, 2003), are examined.
Lactobacilli and bifidobacteria have beta-galactosidase activity thus decreasing the lactose concentration. This is beneficial for people suffering from lactose intolerance. Production of B-complex vitamins by some bifidobacteria strains is significant and noted above. Lactobacilli contribute to the protein degradation through its proteolytic complex and thus facilitate the absorption of proteins by humans. Some bifidobacteria can assimilate inorganic nitrogen and subsequently can lower the concentration of ammonia, which can be carcinogenic at high levels.
Increased accumulation of oxygen radicals in tissues can cause damage to cells. The formation of active oxygen may be associated with factors such as use of certain drugs, increased alcohol consumption, stress and other factors. Increased oxidation is associated with some digestive disorders as well as age, arteriosclerosis, cancerous diseases, etc. The body has several defenses against toxic oxygen, but it is important to consume antioxidants to improve the functioning of these systems. Some microorganisms possess antioxidant enzymes such as SOD (Superoxide dismutases), catalase enzymes, glutathione reductase enzymes and others.
By breaking down milk proteins the lactic acid bacteria release low molecular weight peptides. It was found that some of them inhibit angiotensin-converting enzyme (ACE). ACE cleaves dipeptide from angiotensin I, converting it into angiotensin II (a vasoconstrictor that induces the aldosterone production), which leads to an increase in the concentration of sodium ions and the blood pressure. The best studied effect is the antihypertensive effect of oligopeptides Ile-Pro-Pro and Val-Pro-Pro that are released during proteolytic activity of certain strains of L. helveticus. They induce strong inhibition of ACE. Antihypertensive effect is confirmed in clinical trials.
Currently, there are several commercial probiotics that are used successfully, e.g. L. rhamnosus GG (Saxelin M. Lactobacillus GG—a human probiotic strain with thorough clinical documentation. Food Rev Int 1997, 13:293-313). Another industrial probiotic is L. fermentum 39, used for stabilization of the intestinal microflora during dysbacteriosis (1).
There is a bacterial strain Lactobacillus fermentum ME3, possessing SOD activity and activity against pathogens (Mikelsaar et al., 2007).
A topical problem is the identification and selection of probiotic strains of lactic acid bacteria and using them for preparation of a polybacterial product that has a number of useful properties, such as high survival in the gastrointestinal tract, antioxidant effects, strong adhesion to the epithelial layer of the colon, cholesterol reduction capacity, immune modulating and anti-inflammatory effect, ACE inhibitory activity.
The objective of this invention is to identify and select strains of probiotic lactic acid bacteria with beneficial health properties, which shall be used for the creation of a probiotic preparation that possesses a combination of functional effects.
The probiotic preparation, which is object of the present invention, is a polybacterial combination consisting of three probiotic strains of lactic acid bacteria: Lactobacillus gasseri 7/12, deposited under No. 8720 at the National Bank for Industrial Microorganisms and Cell Cultures (NBIMCC), Lactobacillus plantarum F12, deposited under No. 8722 at NBIMCC and Lactobacillus helveticus A1, deposited under No. 8721 at NBIMCC. The product has a number of health benefits: antioxidant effect; reduction of cholesterol concentration due to hydrolysis of bile salts and direct absorption of cholesterol; anti-inflammatory immune modulating effect by reduction of the level of the proinflammatory cytokine “interleukin-8”; capacity to release bioactive peptides inhibiting the enzyme responsible for the high blood pressure (ACE).
Objects of the invention are also new strains of Lactobacillus gasseri 7/12 NBIMCC No. 8720, Lactobacillus plantarum F12 NBIMCC No. 8722 and Lactobacillus helveticus A1 NBIMCC No. 8721 and their beneficial properties.
The probiotic strain Lactobacillus plantarum F12 NBIMCC No. 8722 possesses both antioxidant activity and a significant adhesion to epithelial cells.
The probiotic strain Lactobacillus gasseri 7/12 NBIMCC No. 8720 possesses a set of the following useful properties: high survival in the gastrointestinal tract, strong adhesion to the epithelial layer of the colon, the capacity to reduce cholesterol and anti-inflammatory effects by reducing the level of proinflammatory cytokine “interleukin-8”.
The probiotic strain Lactobacillus helveticus A1 NBIMCC No. 8721 possesses strong anti-ACE effect.
Object of the invention is the use of new probiotic strains and the probiotic polybacterial preparation in pharmaceutical and food industries in order to prevent socially significant diseases such as: hypertension, arteriosclerosis and hypercholesterolemia, weakened immunity and inflammation processes in the intestinal tract, disturbed balance in the intestinal microflora.
Lactobacillus gasseri 7/12 NBIMCC No. 8720 and Lactobacillus plantarum F12 NBIMCC No. 8722 are isolated from the intestinal tract of healthy volunteers. Lactobacillus helveticus A1 NBIMCC No. 8721 is isolated from homemade white cheese, which proves their GRAS status (generally recognized as safe). Species affiliation and strains identity of the three strains are established through a precise DNA-based methods (2) sequencing of the 16S ribosomal genes, ARDRA, pulse electrophoresis, AFLP.
Phenotypic identification of the three strains is performed using the API 50 CHL System (BioMerieux, France).
Strains are molecularly identified by means of AFLP and pulse electrophoresis. The two main molecular methods, which are used for identification of the three strains and the obtaining of their strain-specific DNA profiles, are described in the abovementioned article (Dimitrov Zh. Et al., 2008). In
Lactobacillus plantarum F12 NBIMCC No. 8722 forms white S-colonies with sizes of 1-2 mm. Bacterial cells are short (0.9 to 1.2×3-8 um) with rounded corners. The major cultivation medium is MRS broth and agar (OXOID). The identification is performed according to the Bergey's Manual (2009) by using the Api web database (API 50CHL strips) and MicroLog M5.1.1 database (Biolog AN Microplate). ARDRA profile is typical for the strain L. plantarum. The profile of soluble cellular protein is identical to that of L. plantarum (ATCC). It grows in MRS broth after inoculation with 0.1%. The cultivation is conducted at 37° C. for about 18-24 hours. The broth medium and atmospheric air do not require any preliminary anaerobization during cultivation. The strain develops for 48 h in an anaerobic environment on MRS agar.
Lactobacillus gasseri 7/12 NBIMCC No. 8720 forms white S-colonies with sizes of 1-2 mm. Bacterial cells are short (0, 6-0.8×3.0-5.0 um) with rounded corners. The major cultivation medium is MRS broth and agar (OXOID). The strain was identified according to the Bergey's Manual (2009) by using the Api web database (API 50CHL strips) and MicroLog M5.1.1 database (Biolog AN Microplate). ARDRA profile is typical for the strain L. gasseri. The profile of soluble cellular proteins is identical to that of strain L. gasseri 33323 (ATCC). Lactobacillus gasseri 7/12 grows on MRS broth after inoculation with 0.1%. The cultivation is conducted at 37° C. for about 18-24 hours. The broth medium and atmospheric air do not require any preliminary anaerobization during cultivation. The strain develops for 48h in an anaerobic environment on MRS agar.
Lactobacillus helveticus A1 NBIMCC No. 8721 forms white R-colonies with sizes of 1-2 mm. Bacterial cells have a length of 3.0-5.0 um. Basic culture media are MRS broth and agar (OXOID) and sterile skimmed milk for microbiological purposes, 10% dry matter (OXOID). The strain is identified according to the Bergey's Manual (2009) by using the Api web database (API 50CHL strips) and MicroLog M5.1.1 database (Biolog AN Microplate). ARDRA profile is typical for L. helveticus. The profile of soluble cellular proteins is identical to that of strain L. helveticus 15009 (ATCC). Lactobacillus helveticus A 1 grows on MRS broth after inoculation with 0.1%. The cultivation is conducted at 37° C. for about 18-24 hours. The broth medium and atmospheric air do not require any preliminary anaerobization during cultivation. The strain develops for 48 h in an anaerobic environment on MRS agar. The strain develops on sterile skimmed milk after inoculation with 0.1% and cultivated at 37° C. for 18-24 hours.
Determination of Antioxidant Effect
The strain L. plantarum F12 has antioxidant properties and as such it is selected from among more than 400 lactobacilli. In order to make the selection, in terms of antioxidant properties, the strains are incubated in MRS broth for 24 hours and centrifuged at 3500 g for 10 min at 4° C. After washing with saline solution the cells are re-suspend in 1.15% KCl to 1×109 cells in 1 ml. Cell suspension is subjected to sonication (Branson B-12 Sonic power Company) for 5 min in an ice bath, followed by 10 min stay at −20° C. The suspension is centrifuged at 10,000 g for 10 min at 4° C. The supernatant is used as acellular extract. Three types of activities are determined:
Total Antioxidant Activity ORAC
The main method for determining total antioxidant activity is ORAC (Oxygen radical absorbance capacity). The result is presented in TROLOX equivalents of 109 microbial cells. The Cao et al (1995) method is used. The principle is as follows: substrate OI-phycoerythrin (Sigma Chemical Co.) is subjected to oxidant attack by radical generator 2.2 vI-azobis(2-amidinopropane)dihydrochloride (AAPH; Waco Chemical USA). The standard solution TROLOX (6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid, Trolox; Aldrich) is prepared by dissolving 5 mg of the substance in 200 ml of 0.2 M phosphate buffer (stock solution). The working solution is obtained by mixing 1 ml of the stock solution with 9 ml of the phosphate buffer.
In the presence of a sample with antioxidant properties the oxidation of phycoerythrin is reduced to some extent. The relative fluorescence is measured using waves with lengths of 535 nm (excitation) and 595 nm (emission), respectively, for a period of 60 minute. The following formula is used:
ORAC value=X K (Ssample−Sblank)/(Strolox−Sblank)
Where X is the sample volume in microliters, and K is the coefficient of dilution. S—the areas of fluorescent curve.
General Antiradical Activity
The substances that capture free radicals are determined for each of the strains based on the degree of reduction in the intensity of staining of the compound 1,1-diphenyl-2-picrilhydrazine (DPPH). The strength of the radical capturing activity is proportional to the degree of discoloration of the purple color of DPPH. The milk fermented with the corresponding strain is centrifuged and the supernatant is extracted with diethyl ether. The process is followed by evaporation of the ether layer and dissolving the residue in methanol. A volume of 0.1 ml of this solution is mixed with 1.4 ml of DPPH solution (40 μg/ml in methanol). Radical capturing activity is defined as a difference in absorbance at 517 nm between an empty sample and the sample [A517 (empty)−A517 (sample)].
SOD Activity
Test is performed pursuant to Chang & Hasan, 1997. The strains grow on broth (M17 for streptococci, MRS for lactobacilli) and after incubation the cultures are centrifuged, washed with phosphate buffer with 0.1 mM EDTA, pH 7.8, re-suspended in the same buffer and then sonicated. Centrifuged at 17000 g and dialyzed against the above phosphate buffer for 24 hours. Centrifuged again at 20000 g. The total protein concentration of acellular extract is determined pursuant to Lowry. Both enzymatic activities are defined using special test kits (SIGMA) according to the manufacturer's instructions. SOD is determined by the cytochrome C method in a conjugated enzyme system with xanthine oxidase. The principle is: xanthine oxidase oxidizes xanthine while cytochrome C is reduced. In the presence of a sample with a SOD activity the reduction of cytochrome C is inhibited to some extent, because the two protons bind to the superoxide radical from SOD instead to be transferred to cytochrome C.
Table 1 presents the results of determination of different antioxidant activities: total antioxidant activity by the ORAC test, total antiradical activity and SOD activity.
Significant total antioxidant activity is found both in intact cells of strain L. plantarum F12, as well as in the acellular extract. In terms of SOD activity acellular extract of this strain surpasses all tested lactobacilli from different bacterial species.
Determination of Adhesion Against Epithelial Cells
Epithelial cell lines Caco-2 and HT29 are cultured as monolayers in DMEM medium (Dilbecco's modified Eagle's medium, Gibco, UK), filled with 10% fetal bovine serum. Incubation temperature is 37° C. in water saturated atmosphere containing 5% CO2. At approximately 90% of a built monolayer the cells undergo passaging through incubation with 0.25% trypsin and 10 mM EDTA solution for 10 min at 37° C. In order to determine adhesion the eukaryotic cells are seeded in 6-well cluster culture dish at a concentration of 2×105 cells/ml. The medium is changed every 2 days for a total of 10 days while the monolayer is built (3-4 days) and cell receptors are maturing. After adhesion the monolayers are washed twice with PBS buffer. Bacterial cultures at a concentration of 108 cells/ml in 2 ml DMEM without antibiotics are added to the monolayers. Incubation for 60 min at 37° C. in a saturated atmosphere containing 5% CO2 is performed. Then the wells are washed five times with PBS and fixed with methanol for 3 minutes. Afterwards Gram staining and microscopic evaluation of adhesion is performed. The number of bacteria adhered to 20 epithelial cells is counted. Test includes reporting of 10 microscope fields.
L. plantarum F12
Determination of Adhesion Against Epithelial Cells
The method is shown above.
L. gasseri 7/12
Determination of Anti-Inflammatory Immunomodulating Effect
Boosting the induction of inflammatory cytokines is highly undesirable in people with inflammatory bowel disease (IBD). Synthesis of inflammatory cytokines is inhibited by the signal peptide Interleukin 10 (IL-10), which is produced by naive T-helper cells or macrophages. The human monocyte cell line U-937 proved to be suitable not only for evaluation of the induction of cytotoxic TNF-α and IL-1, but also in determining the induction of signal peptide IL-10.
The quantitative determination of the expression of the two signal peptide TNF-α and IL-10 of antigen-presenting cells is used for measuring the immunomodulating effect: differentiated macrophages of human monocyte cell line U-937 (ATCC). The maintenance of the cell line is done at 37° C. and 5% CO2 on RPMI 1640 medium (ATCC 30-2001), containing 10% fetal bovine serum (ATCC 30-2020), 4.5 g/l glucose, 10 mM HEPES, 1 mM sodium pyruvate, 2 mM L-glutamine, 1.5 g/l sodium bicarbonate, 100 U/ml penicillin, 100 μg/ml streptomycin. Maintained within the ranged of 2×105 to 1×106 cells per milliliter. Upon reaching a density of about 1×106, cells are centrifuged and the medium is renovated. The cell content, which is reported by a cytometer, is 2×105. In 48-well cluster culture dish 1×106 cells per milliliter (5×105 for the well) can be differentiated to macrophages with the aid of 5 μg/ml PMA (phorbol 12-myristate-13-acetate, SIGMA), added to the growth medium for 48 hours in a CO2 incubator. Differentiated adhered macrophages are washed twice with PBS buffer (Dulbecco's phosphate-buffered saline, GibcoBRL) and incubated with fresh medium for 48 hours without PMA. After aspiration of the medium at each well with adhered macrophages are added 0.5 ml bacterial cells with a concentration of 1×106 per ml, suspended in the growth medium of the macrophages. The cells are incubated for 24 hours in a CO2 incubator.
Assessment of induction of the signal peptide TNF-α of lactic acid bacteria is done by sandwich ELISA. At the end of incubation the supernatant is collected and centrifuged to eliminate bacterial and human cells. 200 μl of the resulting supernatants are used for determination of TNF-α through a special kit of R&D Systems (Human TNF-α/TNFSF1A Immunoassay, Cat. #DTA00C), following manufacturer's instructions. Briefly: immune dishes are covered with a monoclonal antibody against human TNF-α, which holds TNF-α in a special manner. After washing, the wells are treated with a polyclonal antibody against TNF-α, which is connected to the enzyme Horseradish Peroxidase. Afterwards are added the substrates, hydrogen peroxide and tetramethylbenzidine, and after an enzymatic reaction at room temperatures for 20 min at dark the reaction is topped with 2N sulfuric acid. The absorption is measured at 450 nm. For calculation of the TNF-α concentration is used standards and a standard curve is drawn.
Assessment of induction of the signal peptide IL-6 of lactic acid bacteria is done by sandwich ELISA. The principle of detection is analogous to that described above. During the assessment is used analytical ELISA kit and then quantitative evaluation is performed according to the manufacturer's instructions.
Assessment of induction of the signal peptide of IL-10 of lactic acid bacteria is done by sandwich ELISA. During the assessment is used analytical ELISA kit and then quantitative evaluation is performed according to the manufacturer's instructions.
The assessment of the five cytokines TGF-β, IL-8, IL-6, IL-10 and TNFα for each of the isolated strains is performed three times. Table 4 gives the average induction results for the five cytokines. The strain L. gasseri 7/12, which has a moderate adhesion, is the most successful anti-inflammatory strain among the other subjects. He has a good correlation between IL-10 and TNF-α, a significant reduction of IL-8 and TGF-β, and has no significant induction of IL-6. Proinflammatory cytokine IL-8 is synthesized by epithelial cells. For the assessment are used cell lines Caco-2 and HT-29. The increased levels of IL-8 may lead to increased activity of neutrophil cells and hence to inflammatory problems in the colon. The discovery of strains that are able to reduce the level of IL-8 is essential for the establishment of bacterial preparations for the prevention of inflammatory diseases of the gastrointestinal tract. The strain L. gasseri 7/12 is valuable in this regard. The results of stimulation of epithelial cells with L. gasseri 7/12 are presented in Table 5.
L. gasseri 7/12
L. gasseri 7/12
Determination of the Capacity to Reduce Cholesterol Levels
Bile Salt Hydrolase (BSH) Activity
Strains are grown under optimal conditions in broth media as given above, but in broths are added the two most important bile salts: sodium taurocholate (TCA) and sodium glycocholate (GCA). The concentration of salts is 1 mM. They are added after sterilization by microfiltration of the broth. The inoculum is 1% and incubation time is 24 hours. Uninoculated broth is used as a control. BSH activity is measured as deconjugated nanomoles TCA and GCA for 1 minute. The determination is high-performance liquid chromatography (HPLC). The column used is Ultrasphere ODS column, 80 angstrom, 15 cm, 3 μm diameter of the filler grains. The configuration used is SHIMADZU UV detector at 210 nm. Free and conjugated bile acids are detected at a gradient reverse phase mode. Solvent A is 65% methanol in 0.03 M sodium acetate at pH 4.3, adjusted with phosphoric acid. Solvent B is methanol with a HPLC quality. The eluent program is an isocratic step for 8 minutes at 15% eluent B and then linear gradient to 85% for 17 minutes. The process is followed by an isocratic step of 5 minutes at 85%. The injected volume is 10 μl. BSH activity values are expressed in micromoles choline acid (CA) released from 1010 cells per minute and 24 hour incubation time.
Direct Reduction of Cholesterol
The strains are inoculated at a concentration of 1% in the respective media for 24 hours. The broth media contain 0.3% Oxgal and 100 μg of water-soluble cholesterol per ml (cholesterol-PEG600, SIGMA). After incubation the cells are pelleted by centrifugation and 0.5 ml of the supernatant is treated with 4 ml of methanolic 2M KOH by heating for 20 minutes at 80° C. It is extracted with 5 ml of hexane and 4 ml of the hexane layer is transferred into test tubes and evaporated with nitrogen at 60° C. Dry residue is dissolve in 0.5 ml of isopropanol and the cholesterol content is determined with the analytical kit of Boeringer Manhaim. The degree of cholesterol reduction is determined on the basis of uninoculated control media.
Two main activities related to the reduction of cholesterol are examined—direct lowering of cholesterol levels and indirect cholesterol reduction of serum cholesterol as a consequence of deconjugating activity against bile salts (BSH). In the direct elimination of cholesterol, mainly due to the adsorption onto the microorganisms' cell wall components, the residual cholesterol is measured as described in the methodological part. Measuring the concentration of cholesterol is carried out using enzymatic test. Measurements are made three times and the results are averaged. Table 6 presents the results of direct anticholesterol activity expressed as percentage reduction of cholesterol.
L. gasseri 7/12
BSH deconjugating activity indirectly affects on serum cholesterol levels. The strains with BSH activity hydrolyze bile salts and then deconjugated bile acids are transferred to the exit of the intestinal tract. Bile salts are recycled in the body, and after the reduction of their concentration in the liver, part of the cholesterol is switched to the production of bile acids and subsequently bile salts (bile acid conjugates with the amino acids taurine and glycine). In spite of all, the level of serum cholesterol is expected to drop. In Table 7 are given the results of BSH activity of L. gasseri 7/12 after threefold testing and averaging the results.
L. gasseri 7/12
Determination of Capacity for Secretion of Bioactive ACE-Inhibiting Peptides
ACE-Inhibiting Activity
Purified strains with inoculum of 0.1% are incubated for 18 hours in 9% skimmed milk at 37° C. After adjusting the pH to 4.3 with 50% lactic acid the samples are centrifuged (5000 g, 10 min). Supernatant is dosed at reverse-phase cartridge and washed with water. The process is followed by elution with 60% acetonitrile in 0.1% trifluoroacetic acid and then evaporation and reconstitution of the resulting extract. The extract or its dilutions are analyzed for inhibition of ACE.
A total peptide extract is prepared. Enzymatic reaction is carried out by a conventional test, but using different dilutions of peptide extracts as their volume is 20 μl. The enzyme solution was 40 μl with an activity of 0.1 U/ml. The substrate hipuril-histidil-leucine is dissolved in borate buffer at pH 8.3 and has a volume of 190 μl. The final concentration of the substrate is 6 mM, and those of sodium chloride is 300 mM. The reaction is conducted at 37° C. for 30 minutes. The seizing is performed with 100 microliters of 4 n HCl, and the extraction of the freed hippuric acid is done with 1 ml of ethyl acetate. After evaporation of the solvent, the residue is dissolved in 1 ml of water and tested spectrophotometrically at 228 nm.
The percentage of inhibition of ACE enzyme is reported by the formula:
where A is the absorbance under the upper reaction, C is the absorbance without enzyme, B is the absorbance without the involvement of peptide extracts.
Graphs are constructed and on the abscissa are shown microliters of the peptide extract—20, 10, 5, and on the ordinate is shown inhibition as percentages. The strength of inhibitory effect is considered graphically as the volume of peptide extract that is causing 50% inhibition of the ACE enzyme. The smaller volume suggest of a greater ACE inhibiting capacity of the product. Table 8 provides important peptidases activities of the strain L. helveticus A1, which are largely based on the ability of this strain to release bioactive peptides. Table 9 provides ACE-inhibitory activity of L. helveticus A1 in % inhibition of ACE, rounded to the nearest integer.
L. helveticus A1
L. helveticus A1
For L. helveticus A1 is drawn a graph (
The results show that the strain L. helveticus A1 has a strong anti-ACE effect.
Determination of the Sequence of ACE-Inhibiting Peptides from the Strain L. Helveticus A1
Preparation of Concentrated Peptide Extracts
The supernatants of each strain are subjected to centrifugal ultrafiltration through special ultrafiltration cartridges with a molecular mass cutoff of 5000 Da. Low molecular weight hydrophobic and medium hydrophobic peptides, among which is usually looking for anti-ACE representatives, are concentrate on reverse-phase cartridges. In particular, after ultrafiltration of the samples is added trifluoroacetic acid to 0.1% and the mixture is passed through the cartridges. Peptides are retained. After washing with 0.1% TFA follows elution of low molecular weight peptides with 60% acetonitrile in 0.1% TFA. After evaporation the peptides are re-suspend in 10% acetonitrile in 0.1% TFA and dosed on a preparative reverse-phase HPLC column Nucleosil C18. The high-performance liquid, chromatography device SHIMADZU is equipped with two pumps, HPLC column module with the ability to maintain a certain temperature, absorption detector and a fraction collector.
In order to verify the activity, all concentrates are measured for anti-ACE activity.
Coarse Fractionation of Peptide Concentrates After Chromatographic Separation.
Samples injected into the HPLC column, as indicated above, are subjected to reverse-phase gradient fractionation. The acetonitrile gradient is from 0% to 80% in 0.1% TFA. Peptides are detected at a wavelength of 214 nm. By means of a fraction collector are captured fractions of 1 ml. After coarse fractionation these fractions are evaporated in a vacuum centrifuge and re-suspend in 0.1% TFA. The anti-ACE activity of the fractions is tested in order to be selected those fractions that have such activity. The chromatogram that shows the coarse fractionation of peptide concentration of strain L. helveticus A1 is shown in
Refractionation of Selected Fractions for Collecting Purified Peptides After High Performance Reversed Phase Chromatography.
Methodical fine fractionation is performed on the same principle as the coarse fractionation—i.e. reversed phase, but the slope of the gradient is gentler. Gradient conditions for fractions of the strain L. helveticus A1 are 25-35% acetonitrile. The column used is semi-preparative Nucleodur Sphinx.
In
In
Peptide Sequencing
The principle of sequencing is the classical scheme of manual sequencing with phenylisothiocyanate: starting with phenyl thioisocyanate: initial derivatization of amino-terminus of the peptide; cutting off of derivative N-terminal amino acid (CA) using 100% trifluoroacetic acid (TFA); separation by extraction of derivative N-terminal amino acid from the residual peptide; conversion of N-terminal amino acid to phenylthiohydantoin derivative by treatment with 40% (TFA); HPLC analysis of the PTH-amino acid; next cycle for the new N-terminal amino acid. In case of small hydrophobic peptides, the step of separation by extraction of derivative N-terminal amino acid from the residual peptide is impossible. This can be done by preliminary fixing of the C-terminal of the peptide to arylamine-PVDF membrane. Thus, peptide can be sequenced to the last C-terminal amino acids from the N-terminus. Fixing of the peptide from the COOH-terminus is possible after activation of the COOH-terminus by treatment with EDC (ethyl-dimethylaminopropyl carbodiimide) and subsequent reaction of activated carboxyl groups with the arylamine molecule of the membrane. Table 10 presents the sequence of anti-ACE peptides released by the strain L. helveticus A1
L. helveticus A1
Polybacterial preparation contains lyophilized strains of Lactobacillus gasseri 7/12 NBIMCC No. 8720, Lactobacillus plantarum F12 NBIMCC No. 8722 and Lactobacillus helveticus A1 NBIMCC No. 8721. The three strains are grown separately in laboratory fermentation chambers, 5 liters each, for biomass accumulation at milk as a medium, which is hydrolyzed with alkaline protease, supplemented with 0.2% yeast autolysate for nutritive purposes (Springer Biotec), as the amount of the inoculum is 1% and pH is maintained at 5.7 with sodium hydroxide. Incubation continues till the beginning of the stationary phase. With the three cultures containing enriched biomass of about 109 for Lactobacillus plantarum F12, and Lactobacillus helveticus A1, and 2×108 for Lactobacillus gasseri 7/12, an industrial fermenting agent is inoculated in a milk medium that is hydrolyzed with alkaline protease by the addition of 0.2% yeast autolysate for nutritive purposes (Springer Biotec), as the inoculum quantity is 2%. The pH is maintained at 5.7 with sodium hydroxide. The resulting biomass mixture of the three probiotic strains is dosed in an industrial lyophilizer. Sublimation drying is conducted at −28 to −29° C. The final heating is up to 30° C. Residual moisture is 4%. The mixture is packed in an inert (nitrogen) atmosphere. Special measures to reduce the mortality of the strains during the technological cycle are undertaken. The parameters of the fermentation, lyophilization and packaging are optimized. Survival and activity of the strains is controlled by means of modern molecular biology techniques (real-time PCR). The presence and strength of probiotic effects are controlled with high-precision techniques—High-performance liquid chromatography (hydrolysis of bile salts, analysis of bioactive peptides), Gas chromatography (determination of cholesterol-reducing activity), Real-time PCR (determining the vitality of the strains and their number), Spectral equipment (determination of antioxidant activities, detection of immunomodulating activities).
The ready-for-use lyophilized polybacterial preparation contains live bacteria (number of live cells per 1 g) of the three probiotic strains of at least: 109 of Lactobacillus gasseri 7/12, 2×109 of Lactobacillus helveticus A1, 9×109 of Lactobacillus plantarum F12.
In Table 11 are given the results of determination of specific antioxidant activities such as: total antioxidant activity, total antiradical activity, SOD activity of the finished product.
In Table 12 and Table 13 are given the cytokine levels after induction of the human cell lines U-937 and HT-29 by 108/ml bacterial cells of the preparation.
In Table 14 are given anti-cholesterol activities of the polybacterial preparation regarding the capacity for hydrolysis of bile salts and the decrease of cholesterol in percentages.
In Table 15 is given ACE-inhibiting activity of the preparation.
Polybacterial preparation is lyophilized dietary supplement with a unique combination of probiotic properties suitable for the prevention of socially significant diseases such as hypertension, arteriosclerosis and hypercholesterolemia, weakened immunity and inflammation processes in the intestinal tract, disturbed balance in the intestinal microflora. The production of this product requires the sharing of advanced industrial equipment and high-tech research equipment. The principle of production of the product is described in the example.
| Number | Date | Country | Kind |
|---|---|---|---|
| 110932 | May 2011 | BG | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/BG2012/000014 | 5/3/2012 | WO | 00 | 10/30/2013 |
