CN109464653A - A kind of novel prevention sucking pig diarrhea peptase and preparation method thereof - Google Patents

A kind of novel prevention sucking pig diarrhea peptase and preparation method thereof Download PDF

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Publication number
CN109464653A
CN109464653A CN201811599053.4A CN201811599053A CN109464653A CN 109464653 A CN109464653 A CN 109464653A CN 201811599053 A CN201811599053 A CN 201811599053A CN 109464653 A CN109464653 A CN 109464653A
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peptase
sucking pig
diarrhea
novel prevention
pig diarrhea
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肖振州
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Shandong Libang Animal Husbandry Co Ltd
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Shandong Libang Animal Husbandry Co Ltd
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Priority to CN201811599053.4A priority Critical patent/CN109464653A/en
Publication of CN109464653A publication Critical patent/CN109464653A/en
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/04Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/12Cyclic peptides, e.g. bacitracins; Polymyxins; Gramicidins S, C; Tyrocidins A, B or C
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
    • A61K31/198Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7042Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7048Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin, digitoxin or digoxin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/02Peptides of undefined number of amino acids; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/43Enzymes; Proenzymes; Derivatives thereof
    • A61K38/45Transferases (2)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/43Enzymes; Proenzymes; Derivatives thereof
    • A61K38/46Hydrolases (3)
    • A61K38/465Hydrolases (3) acting on ester bonds (3.1), e.g. lipases, ribonucleases
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/43Enzymes; Proenzymes; Derivatives thereof
    • A61K38/46Hydrolases (3)
    • A61K38/48Hydrolases (3) acting on peptide bonds (3.4)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/12Antidiarrhoeals
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12YENZYMES
    • C12Y207/00Transferases transferring phosphorus-containing groups (2.7)
    • C12Y207/01Phosphotransferases with an alcohol group as acceptor (2.7.1)
    • C12Y207/01002Glucokinase (2.7.1.2)
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12YENZYMES
    • C12Y301/00Hydrolases acting on ester bonds (3.1)
    • C12Y301/01Carboxylic ester hydrolases (3.1.1)
    • C12Y301/01003Triacylglycerol lipase (3.1.1.3)

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Immunology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Genetics & Genomics (AREA)
  • General Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Molecular Biology (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

The present invention provides a kind of novel prevention sucking pig diarrhea peptases, consist of the following components in percentage by weight: subtilin 0%-30%;Tyrothricin 10%-20%;Hydrolysising protease 8%-16%;Lipase 10%-20%;Glucokinase 2%-6%;α-amino acid injection-800 2%-8%;Quercitin 2%-8%;Remaining is carrier.By adopting the above-described technical solution, compared with prior art, the invention has the advantages that passing through the specific culture of isolated peptase of beneficial bacterium, inhibit bacterial virus proliferation, accelerate liver metabolism toxin, and repair wounded hepatocytes, achievees the purpose that the prevention birth comprehensive diarrhea of sucking pig.

Description

A kind of novel prevention sucking pig diarrhea peptase and preparation method thereof
Technical field
The present invention relates to agriculture and animal husbandry technical fields.
Specifically, being to be related to a kind of novel prevention sucking pig diarrhea peptase and preparation method thereof.
Background technique
For sucking pig because not yet establishing stable microecosystem in enteron aisle, itself resistance is lower, sensitive to environmental stimuli, easily Invasion and various stress factors by various pathogenic microorganisms are influenced, and sucking pig bacterium is given in especially sow vertical transmission, virus, The pathogenic microorganisms such as toxin and toxin, easily cause 1-3 days watery diarrheas of nascent sucking pig, and the death rate reaches 90-100%.
Such as:
Transmissible gastroenteritis of swine is caused by transmissible gastro-enteritis virus, the pig at various ages can be infected, with 1-3 age in days with cream Pig morbidity and mortality highest, the young age sucking pig death rate is up to 100%.
Sucking pig Huang dysentery is acute, the lethal infectious diseases of nascent sucking pig.Sucking pig in 1 week old is taken place mostly in, with 1-3 days Age is most commonly seen, and disease incidence 90% and the death rate 50% are very high.
Sucking pig paratyphoid, is caused by salmonella infection.Mainly it is mainly in 1-2 monthly age sucking pig.
The red dysentery of sucking pig, was caused by the exotoxin of c-type clostridieum welchii, takes place mostly in the sucking pig within 1 week old, with 1-3 days Age new life sucking pig is common, accidental to be born in 2-4 week old sucking pig below.
The prior art generallys use simple injection or oral antibiotic treatment, beneficial bacterium, the side such as sow antibody passive immunity Method,
Single class antibiotic such as antibiotic trichomonas net, Enrofloxacin, gentamicin, streptomysin, Amoxicillin, sulfamido, terramycin Class, it is only effective to a few virus or bacterium, and it is invalid to other viruses or bacteriums, overall efficiency is beneficial 10% or so Bacterium therapy cannot be colonized rapidly in enteron aisle, and stable intestinal flora balance purpose is not achieved, and antibody passive immunity method belongs to special Qualitative antibody is invalid to toxin and other viruses.
Existing technology solves Single-issue and side effect and is more toxic.
Summary of the invention
It is an object of the invention to overcome the shortcoming of above-mentioned traditional technology, a kind of novel prevention sucking pig abdomen is provided Peptase and preparation method thereof is rushed down, the peptase that this technology is extracted using the fermentation of multiple beneficial bacterium prevents sucking pig by low dose oral Diarrhea.
The purpose of the present invention is what is reached by following technical measures:
A kind of novel prevention sucking pig diarrhea peptase, consists of the following components in percentage by weight:
Subtilin 20%-30%;
Tyrothricin 10%-20%;
Hydrolysising protease 8%-16%;
Lipase 10%-20%;
Glucokinase 2%-6%;
α-amino acid injection-800 2%-8%;
Quercitin 2%-8%;
Remaining is carrier.
As an improvement: it consists of the following components in percentage by weight:
Subtilin 20%;
Tyrothricin 10%;
Hydrolysising protease 8%;
Lipase 20%;
Glucokinase 6%;
α-amino acid injection-800 8%;
Quercitin 8%;
Remaining is carrier.
As an improvement: it consists of the following components in percentage by weight:
Subtilin 30%;
Tyrothricin 20%;
Hydrolysising protease 16%;
Lipase 10%;
Glucokinase 2%;
α-amino acid injection-800 2%;
Quercitin 2%;
Remaining is carrier.
As an improvement: it consists of the following components in percentage by weight:
Subtilin 25%;
Tyrothricin 15%;
Hydrolysising protease 11%;
Lipase 15%;
Glucokinase 4%;
α-amino acid injection-800 5%;
Quercitin 5%;
Remaining is carrier.
As an improvement: the carrier is alumino-silicate.
As an improvement: the following steps are included:
S1, mixing weigh the component of each weight percent weight/power ratio as described in the appended claim 1, are uniformly mixed;
S2, storage.
As an improvement: in step sl, mixing temperature is less than 25 DEG C.
As an improvement: in step sl, antistatic mixing machine is used when mixing.
As an improvement: in step s 2, storage temperature is less than 15 DEG C.
As an improvement: in step s 2, when storage, avoids illumination and ultraviolet light from irradiating.
Action principle of the invention is proteolytic enzymes hydrolize albumen, plays important work to animal bacteria, virus infection With promoting the phagocytosis opsonic action of mononuclear macrophage, neutralizing bacteriotoxin toxicity and combining with viral antigen makes viral mistake Go infection host cell ability.
Protein hydrolysate can mediate conditioning phagocytosis, and body mucosal defense is mainly covered on the surface of intestines and mucous membrane of urinary bladder, Inhibit microorganism to adhere in intestinal mucosa, slow down virus breeding, be important mucosal barrier, to certain viruses, bacteriums and general anti- Original has antibody activity, prevents pathogen from invading body.So protein hydrolysate can have Efficient antibacterial, bacteriolyze, promote phagocytosis and coagulate Collection effect, plays an important role in defence early stage body.
Lipase, lipase are present in the animal and plant and microorganism (such as mould, bacterium) tissue containing fat, rouge Fat enzyme can destroy the cell membrane of bacterium, influence bacterial antigens, and bacterium is made to lose infection cell ability, due to breaking for cell membrane Bad, antibacterial material is easier to enter inside bacterium, inhibits bacterial activity.
Subtilin, molecular formula C66H103N17O16S, off-white color or flaxen powder;It is odorless, bitter;Have draw it is wet Property;It is easily oxidized agent destruction, it in the solution can be by various heavy precipitation of salts.This product is readily soluble in water, dissolves in ethanol, It is insoluble in acetone, chloroform or ether.To gram-positive bacteria and negative cocci, Diplococcus pneumopniae, staphylococcus, gonococcus, Diplococcus meningitidis and conveyor screw etc. have bactericidal effect.
Tyrothricin, molecular formula: C65H85N11O13 is the ring type polypeptide from bacillus brevis-antibiotic mixing Object.It is to the effective topically effective antibiotic of gram-positive bacterium.It sometimes in conjunction with benzocainum 5mg with provide from The alleviation of sore throat.In whole body intake, serious side effect can lead to, therefore, using being confined to local application.
Quercitin, quercitin are a kind of flavonoid monomer compounds being widely present in plant, are had anti-oxidant, anti-swollen The multiple pharmacological effects such as tumor, hypoglycemic, reducing blood lipid.Quercitin has certain anti-inflammatory activity, is mainly shown as cause inflammatory factor Inhibiting effect.
Gene repair damages various types of base and is identified by glucokinase, utilizes specific sequence Column oligonucleotides looks for the sequence matched with it into DNA or RNA, and in connection, repairs damaged cell.
α-amino acid injection-800 can enhance glucose phosphate esterase active, promote phosphatide absorption and the synthesis of brain albumen, make tissue generation The activity of thanking is vigorous, improves blood circulation, increases cerebral blood flow (CBF), enhances cell anti-anoxia ability, restores cell function.
In the present invention, proteolytic enzymes hydrolize albumen is defendd as the early stage of body;Lipase, lipase be present in containing In the animal and plant and microorganism (such as mould, bacterium) tissue of fat, lipase can destroy the cell membrane of bacterium, facilitate withered Lavendustin, tyrothricin and quercitin enter inside bacterium, inhibit bacterial activity or kill bacterium, the mid-term as anti-inflammatory disinfection Means;Glucokinase and α-amino acid injection-800 repair damaged cell, restore cell function, and the end as body is restored.
Three phases synergistic effect, the comprehensive diarrhea of effectively preventing advantageously ensure that the health of sucking pig.
New technology extracts different components by fermentation, and every kind of composition is added by order magnitude range, full and uniform mixing, by big Amount is experiments have shown that and the authentic and valid comprehensive diarrhea of solution.
By adopting the above-described technical solution, compared with prior art, the invention has the advantages that passing through the specific training of beneficial bacterium Nutrient inhibits bacterial virus proliferation, accelerates liver metabolism toxin, and repair wounded hepatocytes, reach and prevent lactogenesis out from peptase The purpose of the comprehensive diarrhea of pig.
Specific embodiment
Embodiment 1: a kind of novel prevention sucking pig diarrhea peptase consists of the following components in percentage by weight:
Subtilin 20%;
Tyrothricin 10%;
Hydrolysising protease 8%;
Lipase 20%;
Glucokinase 6%;
α-amino acid injection-800 8%;
Quercitin 8%;
Remaining is carrier.
The carrier is alumino-silicate.
The preparation method of novel prevention sucking pig diarrhea peptase described in embodiment 1, comprising the following steps:
S1, mixing weigh the component of each weight percent weight/power ratio as described in the appended claim 1, are uniformly mixed;
25 DEG C of mixing temperature;
Antistatic mixing machine is used when mixing.
S2, storage, avoid illumination and ultraviolet light from irradiating by 15 DEG C of storage temperature.
Embodiment 2: a kind of novel prevention sucking pig diarrhea peptase consists of the following components in percentage by weight:
Subtilin 30%;
Tyrothricin 20%;
Hydrolysising protease 16%;
Lipase 10%;
Glucokinase 2%;
α-amino acid injection-800 2%;
Quercitin 2%;
Remaining is carrier.
The carrier is alumino-silicate.
The preparation method of novel prevention sucking pig diarrhea peptase described in embodiment 2, comprising the following steps:
S1, mixing weigh the component of each weight percent weight/power ratio as described in the appended claim 1, are uniformly mixed;
15 DEG C of mixing temperature;
Antistatic mixing machine is used when mixing.
S2, storage, storage temperature avoid illumination and ultraviolet light from irradiating less than 10 DEG C.
Embodiment 3: a kind of novel prevention sucking pig diarrhea peptase consists of the following components in percentage by weight:
Subtilin 25%;
Tyrothricin 15%;
Hydrolysising protease 11%;
Lipase 15%;
Glucokinase 4%;
α-amino acid injection-800 5%;
Quercitin 5%;
Remaining is carrier.
The carrier is alumino-silicate.
The preparation method of novel prevention sucking pig diarrhea peptase described in embodiment 3, comprising the following steps:
S1, mixing weigh the component of each weight percent weight/power ratio as described in the appended claim 1, are uniformly mixed;
5 DEG C of mixing temperature;
Antistatic mixing machine is used when mixing.
S2, storage, storage temperature avoid illumination and ultraviolet light from irradiating less than 5 DEG C.
Experimental example:
Test site: Shandong Weifang.
Experimental animal: it is 3000 total to choose nascent sucking pig.It is divided into 3 groups, every group 1000.One group is set as normal control Group, another group is set as administration control group, and one group is set as test group.
Wherein, novel 3.3 grams of prevention sucking pig diarrhea peptase as described in the present invention are gavaged in test group birth 3 hours, often Its primary, 3 days course for the treatment of, serious person can early, evening respectively gavage it is primary.
In use, the novel prevention sucking pig diarrhea peptase as described in the present invention is diluted using 10% glucose solution To 0.8g/ milliliters.
Wherein, Normal group is normally fed.
Wherein, test group gavages streptomysin, and the dosage of the streptomysin makes according to the different by specifications of streptomysin product With 3 days courses for the treatment of.
As a result it is rolled over point:
Table 1 is test sucking pig diarrhea situation.
Wherein, efficient calculation method is (Normal group diarrhea pig's head number-test group diarrhea pig's head number)/normal right According to a group diarrhea pig's head number.
Wherein, the calculation method of survival rate is (diarrhea pig's head number-death pig's head number)/diarrhea pig's head number.
Experimental result: the effective percentage of novel prevention sucking pig diarrhea peptase of the present invention is 94%-97.5%.
One embodiment of the present invention has been described in detail above, but the content is only preferable implementation of the invention Example, should not be considered as limiting the scope of the invention.It is all according to all the changes and improvements made by the present patent application range Deng should all fall within the scope of the patent of the present invention.

Claims (10)

1. a kind of novel prevention sucking pig diarrhea peptase, it is characterised in that: consist of the following components in percentage by weight:
Subtilin 20%-30%;
Tyrothricin 10%-20%;
Hydrolysising protease 8%-16%;
Lipase 10%-20%;
Glucokinase 2%-6%;
α-amino acid injection-800 2%-8%;
Quercitin 2%-8%;
Remaining is carrier.
2. novel prevention sucking pig diarrhea peptase according to claim 1, it is characterised in that: by the group of following weight percent It is grouped as:
Subtilin 20%;
Tyrothricin 10%;
Hydrolysising protease 8%;
Lipase 20%;
Glucokinase 6%;
α-amino acid injection-800 8%;
Quercitin 8%;
Remaining is carrier.
3. novel prevention sucking pig diarrhea peptase according to claim 1, it is characterised in that: by the group of following weight percent It is grouped as:
Subtilin 30%;
Tyrothricin 20%;
Hydrolysising protease 16%;
Lipase 10%;
Glucokinase 2%;
α-amino acid injection-800 2%;
Quercitin 2%;
Remaining is carrier.
4. novel prevention sucking pig diarrhea peptase according to claim 1, it is characterised in that: by the group of following weight percent It is grouped as:
Subtilin 25%;
Tyrothricin 15%;
Hydrolysising protease 11%;
Lipase 15%;
Glucokinase 4%;
α-amino acid injection-800 5%;
Quercitin 5%;
Remaining is carrier.
5. novel prevention sucking pig diarrhea peptase according to claim 1, it is characterised in that: the carrier is alumino-silicate.
6. the preparation method of novel prevention sucking pig diarrhea peptase as described in claim 1, it is characterised in that: including following step It is rapid:
S1, mixing weigh the component of each weight percent weight/power ratio as described in the appended claim 1, are uniformly mixed;
S2, storage.
7. the preparation method of novel prevention sucking pig diarrhea peptase as claimed in claim 6, it is characterised in that: in step sl, Mixing temperature is less than 25 DEG C.
8. the preparation method of novel prevention sucking pig diarrhea peptase as claimed in claim 6, it is characterised in that: in step sl, Antistatic mixing machine is used when mixing.
9. the preparation method of novel prevention sucking pig diarrhea peptase as claimed in claim 6, it is characterised in that: in step s 2, Storage temperature is less than 15 DEG C.
10. the preparation method of novel prevention sucking pig diarrhea peptase as claimed in claim 6, it is characterised in that: in step s 2, Illumination and ultraviolet light is avoided to irradiate when storage.
CN201811599053.4A 2018-12-26 2018-12-26 A kind of novel prevention sucking pig diarrhea peptase and preparation method thereof Pending CN109464653A (en)

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CN110141659A (en) * 2019-06-10 2019-08-20 山东利邦牧业股份有限公司 A kind of novel enhanced livestock and poultry Abwehrkraft des Koepers activity peptase and preparation method

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110141659A (en) * 2019-06-10 2019-08-20 山东利邦牧业股份有限公司 A kind of novel enhanced livestock and poultry Abwehrkraft des Koepers activity peptase and preparation method

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