CN108794605B - Bioactive polypeptide SRPETSG, and preparation method and application thereof - Google Patents
Bioactive polypeptide SRPETSG, and preparation method and application thereof Download PDFInfo
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- CN108794605B CN108794605B CN201810718874.9A CN201810718874A CN108794605B CN 108794605 B CN108794605 B CN 108794605B CN 201810718874 A CN201810718874 A CN 201810718874A CN 108794605 B CN108794605 B CN 108794605B
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- srpetsg
- aging
- polypeptide
- biologically active
- active polypeptide
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
- C07K14/335—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Lactobacillus (G)
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/17—Amino acids, peptides or proteins
- A23L33/18—Peptides; Protein hydrolysates
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
- A61P39/06—Free radical scavengers or antioxidants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/08—Anti-ageing preparations
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
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Abstract
The invention relates to the field of protein, and in particular relates to a bioactive polypeptide SRPETSG, a preparation method and application thereof. Through in vitro immune function regulation experiments and in vivo anti-aging experiments, the polypeptide SRPETSG is verified to have better immune regulation function and anti-aging activity, on one hand, the bioactive polypeptide SRPETSG can enhance the in vitro proliferation capacity of lymphocytes and macrophages, improve the capacity of an organism for resisting external pathogen infection, and reduce the morbidity of the organism; on the other hand, the activity of an anti-peroxidase system in vivo can be improved, and the function of resisting exogenous stimulation of an organism is enhanced, so that the probability of aging, aging and illness of the organism is reduced, and the method has very important significance for developing foods, health-care products and medicines with immunoregulation function and anti-aging function.
Description
Technical Field
The invention relates to the field of protein, in particular to a bioactive polypeptide SRPETSG, a preparation method and application thereof.
Background
In the process of fermenting the cow milk by the lactic acid bacteria, a part of protein in the cow milk is metabolized and utilized by the lactic acid bacteria, and a series of physiological and biochemical reactions occur, so that the protein is changed into polypeptide or free amino acid which is digested and absorbed by a human body or directly enters the blood circulation of the human body through the absorption and transportation of small intestinal epithelial cells. The lactobacillus also has some self-synthesized protein polypeptide fragments for the bacteria to grow. Among these polypeptides, some have a specific physiological function and are called "bioactive peptides".
It is particularly important to find safe bioactive peptides in natural food sources. In recent years, some food-derived polypeptides, such as short peptides of corn, soybean peptides, milk polypeptides, etc., have been found to have good biological activity. The polypeptides can be obtained through various ways such as microbial fermentation, digestion and enzymolysis and the like, and most of the polypeptides with biological activity consist of 2-20 amino acid residues, have the molecular weight of less than 6000Da and contain a certain amount of hydrophobic amino acids and aromatic amino acids.
Immunoactive peptides are a class of bioactive polypeptides that are first obtained from milk following opioid peptide discovery and demonstrate their physiological activity. Jolles et al found in 1981 for the first time that a hexapeptide with an amino acid sequence Val-Glu-Pro-Ile-Pro-Tyr can be obtained by hydrolyzing human milk protein with trypsin, and in vitro experiments prove that the hexapeptide can enhance the phagocytosis of mouse abdominal cavity macrophages to sheep erythrocytes. Migliore-Samour et al found that the casein-derived hexapeptide Thr-Thr-Met-Pro-Leu-Trp was able to stimulate phagocytosis of murine peritoneal macrophages by sheep red blood cells and to enhance resistance to Klebsiella pneumoniae. Lemna hexandra et al, fed rats with synthetic milk-derived immunoregulatory peptide (PGPIPN), found that phagocytosis of macrophages in the abdominal cavity of rats and immunoregulatory function related to erythrocytes were significantly enhanced.
Researches show that the immune active peptide can not only enhance the immunity of the organism, stimulate the proliferation of lymphocytes of the organism, enhance the phagocytic function of macrophages, promote the release of cell factors, improve the capability of the organism for resisting the infection of external pathogens, reduce the morbidity of the organism, but also can not cause the immune rejection reaction of the organism.
Aging is a natural phenomenon, and the process is often accompanied by changes of antioxidant level, organ tissues and immune factors, wherein cytokines are subjected to complex changes, such as proinflammatory cytokines IL-6, IL-4, TNF-alpha and the like show a growing trend, and IL-6 and TNF-a are considered to play an important role in the process of the senile diseases. With the development of genetics and molecular biology, research on the biological aging mechanism has made favorable progress. Researchers have found that some genes can significantly increase the life span of some model organisms by as much as 6-fold by using single gene mutation experiments in these organisms, such as mice, Drosophila, and caenorhabditis elegans.
The anti-aging peptide has the advantages that the anti-aging peptide is a novel anti-aging agent, has incomparable advantages with amino acid in the aspect of physiological function, can promote or inhibit enzymes in organisms, improve the absorption and utilization of minerals and other nutrient elements, clear away free radicals in the bodies, enhance the self anti-oxidation capability of the organisms and delay aging. Therefore, the nutrition and health care effects of bioactive peptides have become the focus of research on the subjects of scholars at home and abroad. Experiments and researches by meaningful people find that the milk-derived bioactive small peptide can effectively prolong the life of the drosophila and delay the aging of the drosophila, and has better antioxidation effect, and presumably is rich in thiopeptides. The results of Zhou Zhi Hui et al show that the bovine colostrum extract can obviously improve the SOD activity in serum of the elderly, reduce lipid peroxides of the SOD, enhance the oxidation resistance of organisms and have certain anti-aging function.
At present, there are many researches on bioactive polypeptides, for example, chinese patent CN105254738A discloses a milk-derived bioactive polypeptide DELQDKIH derived from β -casein, chinese patent CN105254739A discloses a milk-derived bioactive polypeptide GTQYTD derived from α s 1-casein, and chinese patent CN105254740A discloses a milk-derived bioactive polypeptide NQFYQKF derived from α s 2-casein.
Disclosure of Invention
The invention aims to provide a bioactive polypeptide SRPETSG, and a preparation method and application thereof.
The purpose of the invention can be realized by the following technical scheme:
in the first aspect of the invention, the amino acid sequence of the bioactive polypeptide SRPETSG is Ser-Arg-Pro-Glu-Thr-Ser-Gly, which is shown as SEQ ID NO: 1 is shown.
Preferably, the bioactive polypeptide is derived from lactobacillus helveticus mycoprotein. Specifically derived from LBH-1278. mu.m.1190 LBH-1278. mu.g.1190 ORF LBH-1278. mu.g.1190 LBH-1278. mu.m.1190 type complete len:350(+) LBH-1278: 1-1050(+), and is the amino acid residue at position 29 to 35 of the protein. LBH-1278. mu.m.1190 LBH-1278. mu.g.1190 ORF LBH-1278. mu.g.1190 LBH-1278. mu.m.1190 type complete len:350(+) LBH-1278: 1-1050(+) amino acid sequence as shown in SEQ ID NO: 3, respectively.
The amino acid sequence of the protein LBH-1278. m.1190 LBH-1278. g.1190 ORF LBH-1278. g.1190 LBH-1278. m.1190 type complete len:350(+) LBH-1278: 1-1050(+) and the corresponding nucleotide sequence are known techniques, and the nucleotide fragment encoding the amino acid residues 29 to 35 of this protein encodes the mature biologically active polypeptide SRPETSG.
Preferably, the bioactive polypeptide has an immunoregulatory function and an anti-aging function.
In a second aspect of the present invention, there is provided a nucleotide fragment encoding the biologically active polypeptide SRPETSG, which has the sequence: 5'-tag tcg tcc aga aac cag tgg-3', as shown in SEQ ID NO: 2, respectively.
The third aspect of the invention provides a preparation method of the bioactive polypeptide SRPETSG, which can be artificially synthesized by a genetic engineering method, can be directly obtained from lactobacillus helveticus thallus by a cell crushing, separating and purifying method, and can be directly prepared by chemical synthesis.
In the fourth aspect of the invention, the invention provides the application of the bioactive polypeptide SRPETSG in the preparation of food, health products, medicines or cosmetics with immunoregulation function.
In the fifth aspect of the invention, the application of the bioactive polypeptide SRPETSG in preparing food, health care products or medicines with anti-aging function is provided.
The sixth aspect of the invention provides the application of the bioactive polypeptide SRPETSG in preparing food, health care products or medicines with immune regulation function and anti-aging function.
Specifically, the bioactive polypeptide SRPETSG can be used for preparing cosmetics for reducing free radical damage to skin and medicines for regulating immunity and/or resisting aging; and because the product of the bioactive polypeptide SRPETSG degraded by gastrointestinal tract still has bioactivity, the bioactive polypeptide SRPETSG can also be used for preparing foods such as yoghourt and the like, health-care products for regulating immunity and oral medicines for regulating immunity and/or resisting aging.
In a seventh aspect of the invention, an immunomodulatory product is provided, comprising the biologically active polypeptide SRPETSG or a derivative of the biologically active polypeptide SRPETSG; the immunoregulation product comprises immunoregulation food, immunoregulation health-care products, immunoregulation medicaments or immunoregulation cosmetics; the derivative of the bioactive polypeptide SRPETSG refers to a polypeptide derivative obtained by carrying out modification such as hydroxylation, carboxylation, carbonylation, methylation, acetylation, phosphorylation, esterification or glycosylation on an amino acid side chain group, an amino terminal or a carboxyl terminal of the bioactive polypeptide SRPETSG.
In an eighth aspect of the invention, an anti-aging product is provided, comprising the bioactive polypeptide SRPETSG or a derivative of the bioactive polypeptide SRPETSG; the anti-aging product comprises anti-aging food, anti-aging health care product or anti-aging drug; the derivative of the bioactive polypeptide SRPETSG refers to a polypeptide derivative obtained by carrying out modification such as hydroxylation, carboxylation, carbonylation, methylation, acetylation, phosphorylation, esterification or glycosylation on an amino acid side chain group, an amino terminal or a carboxyl terminal of the bioactive polypeptide SRPETSG.
In the ninth aspect of the invention, a product with both immunoregulation function and anti-aging function is provided, which comprises the bioactive polypeptide SRPETSG or a derivative of the bioactive polypeptide SRPETSG; products with immunoregulatory and anti-aging functions include foods, health products or drugs; the derivative of the bioactive polypeptide SRPETSG refers to a polypeptide derivative obtained by carrying out modification such as hydroxylation, carboxylation, carbonylation, methylation, acetylation, phosphorylation, esterification or glycosylation on an amino acid side chain group, an amino terminal or a carboxyl terminal of the bioactive polypeptide SRPETSG.
The bioactive polypeptide SRPETSG has the beneficial effects that: the bioactive polypeptide SRPETSG has good activity of regulating the immunity of the organism and anti-aging activity; on one hand, the bioactive polypeptide SRPETSG can enhance the in vitro proliferation capacity of lymphocytes and macrophages, improve the capability of an organism for resisting infection of external pathogens and reduce the morbidity of the organism; on the other hand, the activity of an anti-peroxidase system in vivo can be improved, and the function of resisting exogenous stimulation of an organism is enhanced, so that the probability of aging, aging and illness of the organism is reduced, and the method has very important significance for developing dairy products and health care products with immunoregulation function and anti-aging function.
Drawings
FIG. 1: mass chromatogram extraction (m/z 734.3551);
FIG. 2: a secondary mass spectrum of a fragment with a mass to charge ratio of 734.3551;
FIG. 3: the influence of different concentrations of SRPETSG on the reproductive capacity of caenorhabditis elegans;
FIG. 4: nematode growth status at L4 stage under different culture conditions;
FIG. 5: the influence of the biologically active polypeptide SRPETSG on the body length of caenorhabditis elegans;
FIG. 6: the effect of the biologically active polypeptide SRPETSG on caenorhabditis elegans under oxidative stress.
Detailed Description
Before the present embodiments are further described, it is to be understood that the scope of the invention is not limited to the particular embodiments described below; it is also to be understood that the terminology used in the examples is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention.
When numerical ranges are given in the examples, it is understood that both endpoints of each of the numerical ranges and any value therebetween can be selected unless the invention otherwise indicated. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. In addition to the specific methods, devices, and materials used in the examples, any methods, devices, and materials similar or equivalent to those described in the examples may be used in the practice of the invention in addition to the specific methods, devices, and materials used in the examples, in keeping with the knowledge of one skilled in the art and with the description of the invention.
Unless otherwise indicated, the experimental methods, detection methods, and preparation methods disclosed herein all employ techniques conventional in the art of molecular biology, biochemistry, chromatin structure and analysis, analytical chemistry, cell culture, recombinant DNA technology, and related arts. These techniques are well described in the literature, and may be found in particular in the study of the MOLECULAR CLONING, Sambrook et al: a LABORATORY MANUAL, Second edition, Cold Spring Harbor LABORATORY Press, 1989and Third edition, 2001; ausubel et al, Current PROTOCOLS IN MOLECULAR BIOLOGY, John Wiley & Sons, New York, 1987 and periodic updates; the series METHODS IN ENZYMOLOGY, Academic Press, San Diego; wolffe, CHROMATIN STRUCTURE AND FUNCTION, Third edition, Academic Press, San Diego, 1998; (iii) METHODS IN ENZYMOLOGY, Vol.304, Chromatin (P.M.Wassarman and A.P.Wolffe, eds.), Academic Press, San Diego, 1999; and METHODS IN MOLECULAR BIOLOGY, Vol.119, chromatography Protocols (P.B.Becker, ed.) Humana Press, Totowa, 1999, etc.
The invention is described in detail below with reference to the figures and specific embodiments.
EXAMPLE 1 Artificial Synthesis of active peptide SRPETSG
Synthesis of bioactive peptide
1. 3g of RINK resin (degree of substitution 0.3mmol/g) was weighed into a 150ml reactor and soaked with 50ml of Dichloromethane (DCM).
After 2.2 hours, the resin was washed with 3 resin volumes of N-Dimethylformamide (DMF) and then drained, and this was repeated four times and the resin was drained until use.
3. The Fmoc protecting group on the resin was removed by adding a quantity of 20% piperidine (piperidine/DMF: 1:4, v: v) to the reactor and shaking on a decolourising shaker for 20 min. After deprotection, the resin was washed four times with 3 resin volumes of DMF and then drained.
4. And (3) detecting a small amount of resin by a ninhydrin (ninhydrin) method (detecting A and B, respectively, and reacting at 100 ℃ for 1min), wherein the resin is colored, which indicates that the deprotection is successful.
5. Weighing a proper amount of amino acid Ser and a proper amount of 1-hydroxy-benzotriazole (HOBT) into a 50ml centrifuge tube, adding 20ml of DMF to dissolve the amino acid Ser and the 1-hydroxy-benzotriazole (HOBT), then adding 3ml of N, N diisopropyl carbodiimide (DIC) to shake and shake for 1min, adding the solution into a reactor after the solution is clarified, and then placing the reactor into a 30 ℃ shaking table to react.
After 6.2 hours, the column was capped with a suitable amount of acetic anhydride (acetic anhydride: DIEA: DCM ═ 1:1:2, v: v: v) for half an hour, then washed four times with 3 resin volumes of DMF and drained until needed.
7. The Fmoc protecting group on the resin was removed by adding a quantity of 20% piperidine (piperidine/DMF: 1:4, v: v) to the reactor and shaking on a decolourising shaker for 20 min. After deprotection was washed four times with DMF and then drained.
8. And (3) detecting a small amount of resin by a ninhydrin (ninhydrin) method (detecting A and B, respectively, and reacting at 100 ℃ for 1min), wherein the resin is colored, which indicates that the deprotection is successful.
9. Weighing a second proper amount of amino acid and a proper amount of HOBT in a 50ml centrifuge tube, adding 25ml of DMF to dissolve the amino acid and the HOBT, adding 2.5ml of DIC to shake and shake for 1min, adding the solution into a reactor after the solution is clarified, and then placing the reactor in a shaking table at 30 ℃ to react.
After 10.1 hours, a small amount of resin is taken for detection, and the detection is carried out by an indanthrone method (two drops are respectively detected A and B, and the reaction is carried out for 1min at 100 ℃), if the resin is colorless, the reaction is complete; if the resin is colored, the condensation is not complete and the reaction is continued.
11. After the reaction was completed, the resin was washed four times with DMF and then drained, and a certain amount of 20% piperidine (piperidine/DMF ═ 1:4, v: v) was added to the reactor, and the mixture was shaken on a decolorizing shaker for 20min to remove the Fmoc-protecting group from the resin. After the protection is removed, washing with DMF for four times, and then draining to detect whether the protection is removed.
12. Amino acids Arg, Pro, Glu, Thr, Ser and Gly are grafted in sequence according to steps 9-11.
13. After the last amino acid had been grafted, the protection was removed, washed four times with DMF and the resin was drained with methanol. The polypeptide was then cleaved from the resin with 95 cleavage medium (trifluoroacetic acid: 1,2 ethanedithiol: 3, isopropylsilane: water: 95:2:2:1, v: v: v) (10 ml of cleavage medium per gram of resin) and centrifuged four times with glacial ethyl ether (cleavage medium: ethyl ether: 1:9, v: v).
Thus, the bioactive peptide SRPETSG is artificially synthesized.
Confirmation of biologically active peptides
1) UPLC analysis
UPLC conditions were as follows:
the instrument comprises the following steps: waters ACQUITY UPLC ultra-high performance liquid-electrospray-quadrupole-time-of-flight mass spectrometer
Specification of chromatographic column: BEH C18 chromatographic column
Flow rate: 0.4mL/min
Temperature: 50 deg.C
Ultraviolet detection wavelength: 210nm
Sample introduction amount: 2 μ L
Gradient conditions: solution A: water containing 0.1% formic acid (v/v), liquid B: acetonitrile containing 0.1% formic acid (v/v)
2) Mass spectrometric analysis
The mass spectrometry conditions were as follows:
ion mode: ES +
Mass range (m/z): 100-1000
Capillary voltage (Capillary) (kV): 3.0
Sampling cone (V): 35.0
Ion source temperature (. degree. C.): 115
Desolvation temperature (. degree. C.): 350
Desolventizing gas stream (L/hr): 700.0
Collision energy (eV): 4.0
Scan time (sec): 0.25
Inner scan time (sec): 0.02
According to the analysis method, ultra-high performance liquid chromatography-electrospray-quadrupole-time-of-flight mass spectrometry is used for carrying out chromatographic analysis and mass spectrometric analysis on the bioactive peptide SRPETSG, a mass chromatogram extraction diagram is shown in figure 1, a secondary mass spectrogram of the peak and az and by fracture conditions are shown in figures 2 and 3, the polypeptide mass-to-charge ratio of the peak is 734.3551Da, and the retention time is 32.6 min.
3) Results
As can be seen from FIG. 3, according to the cases of az and by fragmentation, the fragment sequence with the mass-to-charge ratio of 734.3551Da obtained through analysis and calculation by Mascot software is Ser-Arg-Pro-Glu-Thr-Ser-Gly (SRPETSG) and is marked as SEQ ID NO: 1. this fragment corresponds to the residue sequence at positions 29-35 of LBH-1278. mu.m.1190 LBH-1278. mu.g.1190 ORF LBH-1278. mu.g.1190 LBH-1278. mu.m.1190 type complete len:350(+) LBH-1278: 1-1050(+) see SEQ ID NO: 3.
example 2 experiment of the Activity of bioactive peptides in regulating the Immunity of the organism
First, MTT method for testing in vitro lymphocyte proliferation capacity experiment of bioactive polypeptide SRPETSG
1. Experimental materials and instruments:
reagents and materials: experimental animals balb/c mice (male 6-8 weeks old, animal experiment center of Shanghai university of transportation, college of agriculture and biology); the biologically active polypeptide SRPETSG obtained in example 1; mouse lymphocyte extract (ex solibao); RPMI1640 medium (purchased from GIBCO); 3- (4, 5-Dimethylthiazol-2) -2, 5-diphenyltetrazolium bromide salt (MTT, available from Amresco, Inc.); concanavalin (ConA, available from Sigma); bovine serum albumin (BSA, available from Genebase); pepsin (available from Sigma); pancreatin (Corolase PP, from AB).
The instrument equipment comprises: LRH-250F Biochemical incubator, Shanghai Hengshi Co., Ltd; GL-22M high speed refrigerated centrifuge, shanghai luxiang instrument centrifuge instruments ltd; hera cell 150 CO2 incubator, Heraeus; dragon Wellscan MK3 microplate reader, Labsystems Inc.; ALPHA 1-2-LD vacuum freeze drier, Christ company; ultra performance liquid chromatography-quadrupole time-of-flight mass spectrometer, waters corporation.
2. The experimental method comprises the following steps:
taking mouse spleen under aseptic condition, extracting mouse lymphocyte with lymphocyte extract, and performing primary culture. The cell density was adjusted to 2.5X 10 with complete RPMI1640 medium6one/mL. To a 96-well cell culture plate were added in sequence: 100 μ L mouse lymphocyte suspension, 100 μ L RPMI1640 complete medium, 20 μ L concanavalin, 100 μ L sample. In addition, a blank control group (PBS with pH7.2-7.4 and 3 mol/L) and a negative control group (500 mu g/mL BSA) are arranged, and the research shows that the blank control group has no influence on the in vitro lymphocyte proliferation. Each set of 3 replicates. At 5% CO2Culturing at 37 deg.C for 68h, adding 20 μ L MTT into each well under aseptic condition, culturing for 4h, carefully removing supernatant, adding 100 μ L dimethyl sulfoxide into each well, incubating at 37 deg.C for 10min, shaking, and measuring absorbance at 570nm with microplate reader.
The in vitro lymphocyte proliferation capacity is expressed by a stimulation index and is calculated as follows:
in the formula: a. the1Absorbance at 570nm for the blank; a. the2Absorbance at 570nm for the negative control, A3The absorbance at 570nm for the experimental group.
3. Experimental results and analysis:
TABLE 1 Effect of the bioactive polypeptide SRPETSG on in vitro lymphocyte proliferation
| Experiment grouping | Stimulation index SI |
| |
1 |
| SRPETSG | 1.212±0.221* |
Note: the number marked as significant difference (P <0.05) compared to the negative control.
The results are shown in Table 1. As can be seen from Table 1, the stimulation index of the bioactive peptide SRPETSG is greater than that of BSA under the condition that the mass concentration of the bioactive peptide SRPETSG is 100 mug/mL, which indicates that the SRPETSG can stimulate the proliferation of lymphocytes of mice in vitro to a certain extent. And the stimulation index of the SRPETSG reaches 1.212, and has a significant difference with a negative control group (P < 0.05). Therefore, the active polypeptide SRPETSG can be considered to have the capacity of remarkably promoting the mouse lymphocyte proliferation, can be used as a health-care product or an additive to eat, and can improve the immunity of animals and human bodies.
Second, macrophage phagocytosis neutral red promoting ability experiment of bioactive polypeptide SRPETSG
1. Experimental reagents and instruments:
reagent: experimental animals balb/c mice (male 6-8 weeks old) were collected at the animal Experimental center of the college of agriculture and biology of Shanghai university of transportation; the biologically active polypeptide SRPETSG obtained in example 1; LPS, purchased from Sigma; neutral red staining solution, produced by Biyuntian biotechnological research institute.
The instrument equipment comprises: LRH-250F Biochemical incubator Shanghai Hengshi Co., Ltd; GL-22M high speed refrigerated centrifuge Shanghai Luxiang apparatus centrifuge Instrument Co., Ltd; hera cell 150 CO2 incubator Heraeus; dragon Wellscan MK3 microplate reader Labsystems.
2. The experimental method comprises the following steps:
the number of the added cells was 2X 106100 mul/hole of cell suspension per ml, adding 200 mul/hole of RPMI1640 complete culture solution (10% FBS) containing active peptide SRPETSG (1mg/ml) after adherent purification as an experimental group, adding 200 mul/hole of RPMI1640 complete culture solution (10% FBS) containing no active peptide for culture as a blank group; and LPS is added into the experimental group and the blank group when the culture time reaches 24h to reach the final concentration of 10 mug/ml; after further culturing for 48h, the cell culture solution was aspirated. After washing the bottom of the well with PBS, 80. mu.l/well of neutral red dye solution at 37 ℃ was added, and after 10 minutes the dye solution was aspirated and washed twice with PBS, 150. mu.l of cell lysate (glacial acetic acid: absolute ethanol ═ 1:1, v/v) was added to each well. After overnight dissolution at 4 ℃ the absorbance value (OD540) was determined at a wavelength of 540 nm.
3. Experimental results and analysis:
TABLE 2 determination of the ability of the biologically active polypeptide SRPETSG to promote phagocytosis of neutral Red by macrophages
| Experiment grouping | Absorbance values for inflammatory group (OD540) |
| Blank group | 0.1072±0.0236 |
| Experimental group | 0.1512±0.0432** |
Note: significant difference compared to negative control (P <0.05)
Significant difference compared with negative control group (P <0.01)
The experimental results are shown in table 2, compared with the blank cell group, the macrophage phagocytosis neutral red blood ability of the inflammation group added with 1mg/ml bioactive polypeptide SRPETSG is obviously increased, and compared with the blank cell group, the macrophage phagocytosis neutral red blood ability has significant difference (P is less than 0.01). The biological active polypeptide SRPETSG has obvious promotion effect on the ability of phagocytizing neutral red by macrophages in vitro under the condition of inflammation.
Example 3 anti-aging Activity assay of bioactive peptides
Experiment on influence of bioactive polypeptide SRPETSG on reproductive capacity of caenorhabditis elegans
1. Experimental reagents and instruments:
reagent: caenorhabditis elegans, subsidiary of the institute for combined Chinese and Western medicine, university of Compound Dane; coli OP50, subsidiary of the university of fudan; agar powder, national drug group chemical reagents limited; yeast powder, national drug group chemical reagents limited; the biologically active polypeptide SRPETSG obtained in example 1.
The instrument equipment comprises: likang RO15 pure water system, Likang biomedical science and technology, Inc.; model G136T Zealway intelligent high temperature sterilization pot, xiamen micro instrument science and technology ltd; THZ-32 type desk type constant temperature oscillator, shanghai smart dense testing equipment ltd; TDL-40B centrifuge, Shanghai' an pavilion scientific instrument factory; luxiang apparatus GL-22M high speed refrigerated centrifuge, Shanghai Luxiang apparatus instruments Ltd; boxun BJ-CD SERIES biosafety cabinet, Shanghai Boxun industries, Inc.; nikko inverted Electron microscope, Nikon corporation.
2. The experimental method comprises the following steps:
(1) preparation of NGM plate
Taking colibacillus strains to streak on an LB plate, picking single colonies in 10ml of LB liquid culture medium, culturing for 24h at 37 ℃ and 200rpm under shaking until OD600 is 0.4 for inoculating NGM plates to feed nematodes. 100 mu L of bacterial liquid is applied to a 60mm NGM plate, and the distance between the edge of the bacterial liquid and the edge of the plate is about 0.5 cm. The coated NGM plates were ready for use overnight at room temperature (21-25 ℃).
(2) Nematode culture
The nematodes used in the experiment are hermaphrodite and grow under standard culture conditions (temperature 20 ℃, humidity 40-60%).
(3) Synchronization treatment of nematodes
1) Bleaching with sodium perchlorate
Preparing a pregnant insect growth plate (more than 80% of insects in the plate are in a reproductive period) 2-3 plates, washing 5ml of M9 buffer solution for 2 times, sucking the buffer solution into a 15ml centrifuge tube, centrifuging at 1000r/min for 3min, and discarding the supernatant. 5ml of fresh contemporaneous bleaching solution was added and shaken vigorously at room temperature for 2.5min to erode the adult worms. Centrifuged and the supernatant discarded. Ensuring that the total treatment time cannot exceed 5min and preventing insect eggs from being damaged. And adding M9 buffer solution to resuspend the precipitate, mixing uniformly, centrifuging, discarding supernatant, and repeating the process for 3 times.
2) Time-limited spawning method
Selecting a plurality of nematodes in the egg laying period in the same plate, wherein the specific quantity is based on the number of the nematodes needing to be synchronized. Under general conditions, one nematode can lay eggs for about 6 within 1 h. After 0.5h incubation in the plates, the nematodes were picked out of the plates and the eggs in the plates were in the same growth phase.
(4) Index measurement
In the experiment, caenorhabditis elegans is used as an animal model, and L4 stage nematodes after the synchronization treatment are picked into NGM plates with corresponding concentrations. Each concentration of at least 8 nematodes, one for each NGM plate, and recorded as day 0, after which the plate is moved to a new plate every day until the nematodes basically no longer lay eggs, and the total number of eggs laid by the nematodes is counted before they enter the egg laying period.
3. Experimental results and analysis:
the results are shown in fig. 3, and the average egg production number is increased to different degrees in the experimental groups fed with different mass concentrations compared with the blank group not fed with the polypeptide SRPETSG. When the concentration of the fed polypeptide SRPETSG is 300mg/L, the average egg laying number of the nematodes is very obviously different (P <0.01) compared with that of a blank group, and when the concentration of the nematode is 400mg/L and 500mg/L, the average egg laying number of the nematodes is only obviously different (P <0.05) compared with that of the blank group, which further proves that the 300mg/L is the optimal concentration of the mixed peptide polypeptide SRPETSG, and the effect of the nematode is not inhibited but weakened along with the increase of the peptide concentration. In conclusion, the polypeptide SRPETSG can obviously improve the reproductive capacity of the nematodes under a certain concentration. Meanwhile, the experimental result shows that the polypeptide SRPETSG300mg/L is the optimal concentration. However, with increasing concentration, the reproductive capacity of the nematodes is no longer significantly improved.
Second, experiment of influence of bioactive polypeptide SRPETSG on body length of caenorhabditis elegans
1. Experimental reagents and instruments:
reagent: caenorhabditis elegans, subsidiary of the institute for combined Chinese and Western medicine, university of Compound Dane; coli OP50, subsidiary of the university of fudan; agar powder, national drug group chemical reagents limited; yeast powder, national drug group chemical reagents limited; the biologically active polypeptide SRPETSG obtained in example 1.
The instrument equipment comprises: likang RO15 pure water system, Likang biomedical science and technology, Inc.; model G136T Zealway intelligent high temperature sterilization pot, xiamen micro instrument science and technology ltd; THZ-32 type desk type constant temperature oscillator, shanghai smart dense testing equipment ltd; TDL-40B centrifuge, Shanghai' an pavilion scientific instrument factory; luxiang apparatus GL-22M high speed refrigerated centrifuge, Shanghai Luxiang apparatus instruments Ltd; boxun BJ-CD SERIES biosafety cabinet, Shanghai Boxun industries, Inc.; nikko inverted Electron microscope, Nikon corporation.
2. The experimental method comprises the following steps:
(1) preparation of NGM plate
Taking colibacillus strains to streak on an LB plate, picking single colonies in 10ml of LB liquid culture medium, culturing for 24h at 37 ℃ and 200rpm under shaking until OD600 is 0.4 for inoculating NGM plates to feed nematodes. 100 mu L of bacterial liquid is applied to a 60mm NGM plate, and the distance between the edge of the bacterial liquid and the edge of the plate is about 0.5 cm. The coated NGM plates were ready for use overnight at room temperature (21-25 ℃).
(2) Nematode culture
The nematodes used in the experiment are hermaphrodite and grow under standard culture conditions (temperature 20 ℃, humidity 40-60%).
(3) Synchronization treatment of nematodes
1) Bleaching with sodium perchlorate
Preparing a pregnant insect growth plate (more than 80% of insects in the plate are in a reproductive period) 2-3 plates, washing 5ml of M9 buffer solution for 2 times, sucking the buffer solution into a 15ml centrifuge tube, centrifuging at 1000r/min for 3min, and discarding the supernatant. 5ml of fresh contemporaneous bleaching solution was added and shaken vigorously at room temperature for 2.5min to erode the adult worms. Centrifuged and the supernatant discarded. Ensuring that the total treatment time cannot exceed 5min and preventing insect eggs from being damaged. And adding M9 buffer solution to resuspend the precipitate, mixing uniformly, centrifuging, discarding supernatant, and repeating the process for 3 times.
2) Time-limited spawning method
Selecting a plurality of nematodes in the egg laying period in the same plate, wherein the specific quantity is based on the number of the nematodes needing to be synchronized. Under general conditions, one nematode can lay eggs for about 6 within 1 h. After 0.5h incubation in the plates, the nematodes were picked out of the plates and the eggs in the plates were in the same growth phase.
(4) Index measurement
Grouping experiments: blank and polypeptide groups. The difference between the body lengths of different groups of nematodes in the same period can reflect the influence of the active substance on the growth and development of the nematodes to a certain extent. When the nematodes cultured in each group in a synchronized way grow to the L2 stage (about 2 days of culture), 40 nematodes are respectively picked to the respective NGM flat plates, the growth state of the nematodes is observed by an inverted microscope for 2 days, 3 days, 4 days, 5 days, 6 days, 8 days and 10 days, the body length of the nematodes is measured and recorded, and the average value of each group is taken.
3. Experimental results and analysis:
the body length of the nematodes at each time point was measured under the culture condition of 20 ℃ from the L2 stage (day 2) of nematode growth, L3 stage (day 3), L4 stage (day 4), adult stage (day 6), for 8 consecutive days, until day 10 of nematode growth. As can be seen from the combination of FIG. 4 and FIG. 5, the body lengths of all the nematodes in each group are about 1000 μm at the L4 stage, and no obvious difference exists. Meanwhile, as can be seen from the body length variation curve of the nematode, the body length variation curve of the experimental group is almost coincident with that of the blank group, and at the L3 stage (day 3), although the average body length of the nematode is slightly different, the average body length of the nematode does not show a statistically significant difference. Experiments show that the concentration of the polypeptide SRPETSG does not influence the growth of the nematode. Meanwhile, nematodes were found to grow most rapidly in stages from L3 (day 3) to L4 (day 4).
Third, the experiment of the acute oxidative stress survival rate of the bioactive polypeptide SRPETSG
1. Experimental reagents and instruments:
reagent: caenorhabditis elegans, subsidiary of the institute for combined Chinese and Western medicine, university of Compound Dane; coli OP50, subsidiary of the university of fudan; agar powder, national drug group chemical reagents limited; yeast powder, national drug group chemical reagents limited; 30% hydrogen peroxide solution, national pharmaceutical group chemical reagents ltd; the biologically active polypeptide SRPETSG obtained in example 1.
The instrument equipment comprises: likang RO15 pure water system, Likang biomedical science and technology, Inc.; model G136T Zealway intelligent high temperature sterilization pot, xiamen micro instrument science and technology ltd; THZ-32 type desk type constant temperature oscillator, shanghai smart dense testing equipment ltd; TDL-40B centrifuge, Shanghai' an pavilion scientific instrument factory; luxiang apparatus GL-22M high speed refrigerated centrifuge, Shanghai Luxiang apparatus instruments Ltd; boxun BJ-CD SERIES biosafety cabinet, Shanghai Boxun industries, Inc.; nikko inverted Electron microscope, Nikon corporation.
2. The experimental method comprises the following steps:
(1) preparation of NGM plate
Taking colibacillus strains to streak on an LB plate, picking single colonies in 10ml of LB liquid culture medium, culturing for 24h at 37 ℃ and 200rpm under shaking until OD600 is 0.4 for inoculating NGM plates to feed nematodes. 100 mu L of bacterial liquid is applied to a 60mm NGM plate, and the distance between the edge of the bacterial liquid and the edge of the plate is about 0.5 cm. The coated NGM plates were ready for use overnight at room temperature (21-25 ℃).
(2) Nematode culture
The nematodes used in the experiment are hermaphrodite and grow under standard culture conditions (temperature 20 ℃, humidity 40-60%).
(3) Synchronization treatment of nematodes
1) Bleaching with sodium perchlorate
Preparing a pregnant insect growth plate (more than 80% of insects in the plate are in a reproductive period) 2-3 plates, washing 5ml of M9 buffer solution for 2 times, sucking the buffer solution into a 15ml centrifuge tube, centrifuging at 1000r/min for 3min, and discarding the supernatant. 5ml of fresh contemporaneous bleaching solution was added and shaken vigorously at room temperature for 2.5min to erode the adult worms. Centrifuged and the supernatant discarded. Ensuring that the total treatment time cannot exceed 5min and preventing insect eggs from being damaged. And adding M9 buffer solution to resuspend the precipitate, mixing uniformly, centrifuging, discarding supernatant, and repeating the process for 3 times.
2) Time-limited spawning method
Selecting a plurality of nematodes in the egg laying period in the same plate, wherein the specific quantity is based on the number of the nematodes needing to be synchronized. Under general conditions, one nematode can lay eggs for about 6 within 1 h. After 0.5h incubation in the plates, the nematodes were picked out of the plates and the eggs in the plates were in the same growth phase.
(4) Index measurement
Grouping experiments: blank and polypeptide groups. The L4 stage nematodes after the synchronization treatment were placed in corresponding NGM plates and tested in the presence of 20mM H2O2The number of each plate is not less than 10, the number of dead nematodes and the number of survival nematodes are counted every half an hour, and the judgment standard of nematode death is as follows: there was no movement and swallowing, and there was no reaction after light touch. Rejection standard: firstly, escaping to the flat wall or the cover to be dried; secondly, hatching the eggs in vivo to form bag-like insects: ③ drilling into agar.
3. Experimental results and analysis:
TABLE 3 Effect of the bioactive polypeptide SRPETSG on nematodes under oxidative stress
As can be seen from Table 3, the average life span of the nematodes under oxidative stress in the experimental group is significantly improved (P <0.05), and the polypeptide SRPETSG group shows extremely significant difference (P < 0.05). Half of the death time of each group is correspondingly prolonged to a certain extent, and the mixed peptide group shows a remarkable improvement compared with other experimental groups (P < 0.05). As shown in fig. 6, the survival rate of the experimental group was significantly higher than that of the blank group under oxidative stress condition. This indicates that the survival rate of nematodes is significantly improved under oxidative stress, probably because the polypeptide SRPETSG is effective in helping nematodes resist oxidative damage, scavenge free radicals produced in the body and reduce the accumulation of peroxides, rather than by enhancing their heat resistance. The prolongation of the life of the organism is due to the improvement of the resistance of cells to stress conditions to a certain extent, so that the delay of aging is greatly related to the survival rate under the stress conditions. The experimental result proves that the polypeptide SRPETSG can obviously increase the pressure stress and the oxidative stress capability of the nematodes, improve the survival rate of the nematodes and show that the polypeptide SRPETSG with a certain concentration has the anti-aging effect on the nematodes.
The embodiments described above are described to facilitate an understanding and use of the invention by those skilled in the art. It will be readily apparent to those skilled in the art that various modifications to these embodiments may be made, and the generic principles described herein may be applied to other embodiments without the use of the inventive faculty. Therefore, the present invention is not limited to the above embodiments, and those skilled in the art should make improvements and modifications within the scope of the present invention based on the disclosure of the present invention.
Sequence listing
<110> Zhejiang ghui peptide Life health science and technology Limited; shanghai platinum Biotech Ltd
<120> bioactive polypeptide SRPETSG, and preparation method and application thereof
<160> 3
<170> SIPOSequenceListing 1.0
<210> 1
<211> 7
<212> PRT
<213> Artificial Sequence (Artificial Sequence)
<400> 1
Ser Arg Pro Glu Thr Ser Gly
1 5
<210> 2
<211> 21
<212> DNA
<213> Artificial Sequence (Artificial Sequence)
<400> 2
tagtcgtcca gaaaccagtg g 21
<210> 3
<211> 349
<212> PRT
<213> Artificial Sequence (Artificial Sequence)
<400> 3
Met Asn Arg Tyr Lys Asp Ala Gly Val Asp Val Glu Ala Gly Tyr Asp
1 5 10 15
Leu Val Lys Arg Ile Lys Lys Asp Ile Ala Ala Thr Ser Arg Pro Glu
20 25 30
Thr Ser Gly Thr Ile Gly Ser Phe Gly Gly Met Phe Asp Leu Glu Lys
35 40 45
Leu Gly Tyr Gln His Pro Val Leu Val Ser Gly Thr Asp Gly Val Gly
50 55 60
Thr Lys Leu Met Ile Ala Gln Glu Met Gly Ile Asn Asp Thr Ile Gly
65 70 75 80
Ile Asp Cys Val Ala Met Cys Val Asn Asp Val Leu Ala Gln Gly Ala
85 90 95
Glu Pro Leu Phe Phe Leu Asp Tyr Ile Ala Thr Gly His Asn Asp Pro
100 105 110
Ala Lys Leu Ala Gln Val Val His Gly Val Ala Glu Gly Cys Arg Gln
115 120 125
Ser Gly Ser Ala Leu Ile Gly Gly Glu Thr Ala Glu Met Pro Asp Met
130 135 140
Tyr Pro Lys Asn Glu Tyr Asp Leu Ala Gly Phe Ser Thr Gly Ile Ala
145 150 155 160
Asn Lys Glu Asp Ile Leu Thr Gln Asp Leu Ala Lys Glu Gly Asp Ile
165 170 175
Leu Ile Gly Leu Pro Ser Ser Gly Val His Ser Asn Gly Phe Ser Leu
180 185 190
Ile Arg Gln Val Leu Phe Lys Asp His His Leu Lys Val Thr Asp Arg
195 200 205
Pro Glu Ala Leu Glu Gly Lys Ser Ile Gly Glu Ile Leu Leu Thr Pro
210 215 220
Thr Lys Ile Tyr Val Gln Ala Val Leu Ser Leu Val Lys Arg His Leu
225 230 235 240
Leu His Gly Ile Ala His Ile Thr Gly Gly Gly Leu Ile Glu Asn Leu
245 250 255
Pro Arg Thr Tyr Asn Asp Asp Leu Gln Ala Glu Val Asn Leu Gly Ala
260 265 270
Trp Pro Val Gln Ala Ile Phe Arg Tyr Leu Gln Asn Lys Gly Gln Leu
275 280 285
Lys Glu Gln Asp Cys Leu Asn Thr Phe Asn Met Gly Ile Gly Leu Val
290 295 300
Leu Leu Val Pro Lys Ala Asn Val Leu Gln Val Lys Glu Gln Leu Lys
305 310 315 320
Gln Lys Asn Glu Gln Tyr Tyr Glu Ile Gly Lys Leu Arg Lys Arg Pro
325 330 335
Ile Gly Glu Lys Lys Ile Val Phe Asn Gly Ser Phe Lys
340 345
Claims (9)
1. A bioactive polypeptide SRPETSG is characterized in that the amino acid sequence of the polypeptide SRPETSG is Ser-Arg-Pro-Glu-Thr-Ser-Gly.
2. A nucleotide fragment encoding the biologically active polypeptide SRPETSG of claim 1, wherein the nucleotide fragment has the sequence of SEQ ID NO: 2, respectively.
3. The method for preparing the bioactive polypeptide SRPETSG of claim 1, which is artificially synthesized by a genetic engineering method or directly prepared by chemical synthesis.
4. The use of the biologically active polypeptide SRPETSG according to claim 1, wherein the biologically active polypeptide SRPETSG is used for preparing food, health products, drugs or cosmetics with immunoregulatory function.
5. The use of the biologically active polypeptide SRPETSG according to claim 1, wherein the biologically active polypeptide SRPETSG is used for preparing food, health care products or medicines with anti-aging function.
6. The use of the biologically active polypeptide SRPETSG according to claim 1, wherein the biologically active polypeptide SRPETSG is used for preparing food, health care products or medicines with immunoregulatory and anti-aging functions.
7. An immunomodulatory product comprising the biologically active polypeptide of claim 1, SRPETSG; the immunoregulation product comprises an immunoregulation food, an immunoregulation health product, an immunoregulation medicament or an immunoregulation cosmetic.
8. An anti-aging product comprising the biologically active polypeptide SRPETSG of claim 1; the anti-aging product comprises anti-aging food, anti-aging health care products or anti-aging drugs.
9. A product having immunomodulatory and anti-aging properties, comprising the biologically active polypeptide SRPETSG of claim 1; the product with immunoregulation function and anti-aging function comprises food, health product or medicine.
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| CN112745379A (en) * | 2021-01-22 | 2021-05-04 | 浙江辉肽生命健康科技有限公司 | Bioactive peptide with amino acid structure RDNKKTRIIPR, and preparation method and application thereof |
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| CN105254750B (en) * | 2015-10-16 | 2019-01-08 | 浙江辉肽生命健康科技有限公司 | A kind of biologically active polypeptide FGYSGAFKCL and its preparation and application |
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