CN116686903B - Complex bacterial enzyme biological starter and application thereof - Google Patents
Complex bacterial enzyme biological starter and application thereof Download PDFInfo
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- 239000007788 liquid Substances 0.000 claims abstract description 44
- 239000002131 composite material Substances 0.000 claims abstract description 43
- 238000000855 fermentation Methods 0.000 claims abstract description 36
- 241000894006 Bacteria Species 0.000 claims abstract description 33
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- 238000001914 filtration Methods 0.000 claims description 5
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K10/00—Animal feeding-stuffs
- A23K10/10—Animal feeding-stuffs obtained by microbiological or biochemical processes
- A23K10/12—Animal feeding-stuffs obtained by microbiological or biochemical processes by fermentation of natural products, e.g. of vegetable material, animal waste material or biomass
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K10/00—Animal feeding-stuffs
- A23K10/10—Animal feeding-stuffs obtained by microbiological or biochemical processes
- A23K10/14—Pretreatment of feeding-stuffs with enzymes
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K10/00—Animal feeding-stuffs
- A23K10/30—Animal feeding-stuffs from material of plant origin, e.g. roots, seeds or hay; from material of fungal origin, e.g. mushrooms
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K10/00—Animal feeding-stuffs
- A23K10/30—Animal feeding-stuffs from material of plant origin, e.g. roots, seeds or hay; from material of fungal origin, e.g. mushrooms
- A23K10/33—Animal feeding-stuffs from material of plant origin, e.g. roots, seeds or hay; from material of fungal origin, e.g. mushrooms from molasses
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K10/00—Animal feeding-stuffs
- A23K10/30—Animal feeding-stuffs from material of plant origin, e.g. roots, seeds or hay; from material of fungal origin, e.g. mushrooms
- A23K10/37—Animal feeding-stuffs from material of plant origin, e.g. roots, seeds or hay; from material of fungal origin, e.g. mushrooms from waste material
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
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- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/20—Inorganic substances, e.g. oligoelements
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- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K50/00—Feeding-stuffs specially adapted for particular animals
- A23K50/30—Feeding-stuffs specially adapted for particular animals for swines
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P60/00—Technologies relating to agriculture, livestock or agroalimentary industries
- Y02P60/80—Food processing, e.g. use of renewable energies or variable speed drives in handling, conveying or stacking
- Y02P60/87—Re-use of by-products of food processing for fodder production
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Abstract
The application discloses a compound bacteria enzyme biological starter and application thereof, belonging to the field of microbial fermentation. The complex bacterial enzyme biological starter is prepared from complex bacterial liquid, alfalfa extract and pectase according to the weight ratio of 1: (0.5-2): mixing the components (1-3); the composite bacterial liquid is prepared from bacillus subtilis and streptococcus thermophilus according to the weight ratio of 1:1, and is compounded according to the proportion. According to the application, the composite bacteria combination commonly used in the fermented feed is compounded with pectase and alfalfa extract to obtain the starter, and the prepared composite bacteria antibiotic-free fermented feed can remarkably improve the pork quality of growing-finishing pigs after being fed by the synergistic fermentation of the pectase, the alfalfa extract and the alfalfa extract.
Description
Technical Field
The application belongs to the field of microbial fermentation, and particularly relates to a compound bacterium enzyme biological starter and application thereof.
Background
Antibiotic-free cultivation is short for antibiotic-free cultivation, and refers to the fact that any kind of antibiotics are not used in the cultivation process, in particular to the fact that human antibiotics and livestock antibiotics are not used. The antibiotic-free fermented feed is a biological fermented feed which integrates microorganism and compound enzyme microbial starter, and converts feed raw materials into microorganism bacterial protein, bioactive small peptide amino acid, microorganism active probiotics and compound enzyme preparation. The product can not only make up for amino acid which is easy to lack in the conventional feed, but also enable the nutritional ingredients of other coarse feed raw materials to be quickly converted, promote the reproduction of intestinal flora and inhibit the growth of pathogenic microorganisms, thereby replacing the use of antibiotics in daily ration and reducing the threat of the antibiotics to the environment and food safety. Antibiotic-free feeding of live pigs is a major trend and is a necessary requirement of related policy and regulations. At present, the adopted antibiotic-free feed mainly comprises the following modes: the treatment of the raw materials mainly comprises soybean puffing, corn puffing and the like.
The addition of enzyme preparations is also one of the methods for preparing antibiotic-free feed. The enzyme preparation is a biological product with catalytic function after purification and processing, is mainly used for catalyzing various chemical reactions in the production process, has the characteristics of high catalytic efficiency, high specificity, mild acting condition, energy consumption reduction, chemical pollution reduction and the like, is derived from organisms, is generally safer, and can be used in proper amount according to production needs. The enzyme preparation is added into the nonreactive fermented feed, and the digestion of the feed in the body is promoted by the enzyme preparation, so that the residence time in the gastrointestinal tract is shortened, and the opportunity of being utilized by the growth of harmful bacteria can be reduced.
The plant extract contains multiple active ingredients such as polyphenol, flavonoid, polysaccharide, etc., and has various biological properties such as antioxidant, antiinflammatory, and immunoregulatory. Recent studies have shown that plant extracts not only can enhance animal growth performance, but also play an important role in improving meat quality and flavor.
The application patent with publication number of CN114916613A discloses a composition of Chinese herbal medicine for replacing antibiotics and a preparation method of feed thereof; the application discloses a preparation process of a biological microbial inoculum capable of replacing feed antibiotics, which is disclosed in the publication No. CN 112725197B. Said application uses Chinese herbal medicine and living bacteria agent to prepare antibiotic-free feed. However, no report on the preparation of antibiotic-free feed by compounding a composite microbial inoculum, a plant extract and an enzyme preparation is currently seen.
Disclosure of Invention
Aiming at the defects of the prior art, the application aims to provide a complex bacterial enzyme biological starter and application thereof.
In order to achieve the above purpose, the application adopts the following technical scheme:
the application provides a complex bacterial enzyme biological starter, which is characterized by comprising complex bacterial liquid, alfalfa extract and pectinase according to the weight ratio of 1: (0.5-2): mixing the components (1-3); the composite bacterial liquid is prepared from bacillus subtilis and streptococcus thermophilus according to the weight ratio of 1:1, and is compounded according to the proportion.
Preferably, the viable count of Streptococcus thermophilus in the composite bacterial liquid is (1.5-2) multiplied by 10 10 CFU/g, the viable count of bacillus subtilis is (1-1.5). Times.10 10 CFU/g。
Preferably, the alfalfa extract is prepared by the following method:
drying and pulverizing herba Medicaginis, adding 10 times of ethanol solution into pulverized herba Medicaginis, reflux extracting for 2 hr, recovering ethanol from extractive solution, adding aluminum oxide to adsorb impurities, filtering, collecting filtrate, and spray drying the filtrate to obtain herba Medicaginis extract.
In a second aspect, the application provides an application of the complex bacterium enzyme biological starter in complex bacterium antibiotic-free fermented feed.
Preferably, the composite bacteria enzyme starter, brown sugar and water are added into the fermentation bed charge, and the mixture is uniformly mixed, and is subjected to aerobic fermentation for 6-8 hours and anaerobic fermentation for 10-14 days to prepare the composite bacteria antibiotic-free fermented feed.
Preferably, the fermentation base material consists of the following raw materials in parts by weight: 60 parts of corn flour, 24 parts of bean pulp, 10 parts of bran, 18 parts of corncob, 2 parts of molasses, 5 parts of rice bran, 1 part of ammonium sulfate and 5 parts of stone powder.
Preferably, the weight ratio of the complex bacterial enzyme starter, the brown sugar, the water and the fermentation base material is (0.05-0.2): (5-50): (10-50): (50-200).
Preferably, the aerobic fermentation conditions are as follows: the anaerobic fermentation conditions are that the temperature is 20-25 ℃, the ventilation rate is 2-3.5L/min: sealing and fermenting at 35-38deg.C.
The application has the beneficial effects that:
according to the application, the complex bacteria commonly used in the fermented feed are compounded with the pectase and the alfalfa extract to obtain the complex bacteria enzyme starter, on one hand, the pectase and the alfalfa extract not only can add nutrients to the feed, but also can be used as carriers of complex bacteria liquid, so that the complex bacteria is prevented from being inactivated; on the other hand, the composite bacteria antibiotic-free fermented feed prepared by fermenting the starter can obviously improve the pork quality of growing-finishing pigs after being fed.
Detailed Description
It should be noted that the following detailed description is illustrative and is intended to provide further explanation of the application. 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 application belongs.
In the process of selecting raw materials, referring to a feed additive variety catalog (2013), the inventor firstly selects bacillus subtilis and streptococcus thermophilus which are commonly used for fermenting feed as compound bacterial liquid, then carries out a compounding experiment on the compound bacterial liquid, a plant extract and an enzyme preparation recorded in the feed additive variety catalog (2013), finally discovers that the compound bacterial liquid has a synergistic effect after being compounded with alfalfa extract and pectase, and the pork quality of growing-finishing pigs can be effectively improved by using the feed prepared by fermenting the three materials.
In order to enable those skilled in the art to more clearly understand the technical scheme of the present application, the technical scheme of the present application will be described in detail with reference to specific embodiments.
In the following examples and comparative examples, the bacillus subtilis used was purchased from China Center for Type Culture Collection (CCTCC) AB 130010, and after the bacillus subtilis was activated and cultured, a bacillus subtilis bacterial liquid was obtained; streptococcus thermophilus is purchased from China Center for Type Culture Collection (CCTCC) AB 2010206, and after the Streptococcus thermophilus is activated and cultured, streptococcus thermophilus bacterial liquid is obtained; pectase was purchased from Shanghai Seiyaka Biotechnology Co., ltd., specification BR,50000u/g.
The formula and the conditions of the culture medium of the bacillus subtilis are as follows: 100g of glucose, 20g of soybean peptone, 5g of NaCl, 1000mL of distilled water, pH of 7.0, culture time of 20h and culture temperature of 37 ℃; the culture medium formula and conditions of streptococcus thermophilus are as follows: 7.5g of yeast extract, 7.5g of peptone, 10g of glucose and KH 2 PO 4 2g, 100ml of tomato juice, 80ml of tween, 900ml of distilled water, pH of 7.0 and incubation time of 24h.
The fermentation base materials in the application examples and the comparative examples consist of the following raw materials in parts by weight: 60 parts of corn flour, 24 parts of bean pulp, 10 parts of bran, 18 parts of corncob, 2 parts of molasses, 5 parts of rice bran, 1 part of ammonium sulfate and 5 parts of stone powder.
Example 1: and (3) preparing the complex bacterial enzyme biological starter.
(1) Drying and pulverizing herba Medicaginis, adding 10 weight times of ethanol solution (volume fraction 60%) into pulverized herba Medicaginis, and reflux extracting for 2 hr; recovering ethanol from the extractive solution, adding aluminum oxide to adsorb impurities, filtering, collecting filtrate, and spray drying the filtrate to obtain herba Medicaginis extract.
(2) The bacillus subtilis bacterial liquid and the streptococcus thermophilus bacterial liquid are mixed according to the following proportionThe weight ratio of the light to the light is 1:1, and then mixing the composite bacterial liquid, the alfalfa extract and the pectase according to the weight ratio of 1:0.5:1, mixing the materials in proportion to obtain a starter; the viable count of the streptococcus thermophilus in the composite bacterial liquid is 1.5x10 10 CFU/g, viable count of bacillus subtilis is 1×10 10 CFU/g。
Example 2: and (3) preparing the complex bacterial enzyme biological starter.
(1) Drying and pulverizing herba Medicaginis, adding 10 weight times of ethanol solution (volume fraction 60%) into pulverized herba Medicaginis, and reflux extracting for 2 hr; recovering ethanol from the extractive solution, adding aluminum oxide to adsorb impurities, filtering, collecting filtrate, and spray drying the filtrate to obtain herba Medicaginis extract.
(2) The bacillus subtilis bacterial liquid and the streptococcus thermophilus bacterial liquid are mixed according to the weight ratio of 1:1, and then mixing the composite bacterial liquid, the alfalfa extract and the pectase according to the weight ratio of 1:1:2, mixing the materials in proportion to obtain a starter; the viable count of the streptococcus thermophilus in the composite bacterial liquid is 1.8x10 10 CFU/g, viable count of bacillus subtilis is 1.4X10 10 CFU/g。
Example 3: and (3) preparing the complex bacterial enzyme biological starter.
(1) Drying and pulverizing herba Medicaginis, adding 10 weight times of ethanol solution (volume fraction 60%) into pulverized herba Medicaginis, and reflux extracting for 2 hr; recovering ethanol from the extractive solution, adding aluminum oxide to adsorb impurities, filtering, collecting filtrate, and spray drying the filtrate to obtain herba Medicaginis extract.
(2) The bacillus subtilis bacterial liquid and the streptococcus thermophilus bacterial liquid are mixed according to the weight ratio of 1:1, and then mixing the composite bacterial liquid, the alfalfa extract and the pectase according to the weight ratio of 1:2:3, mixing the materials in proportion to obtain a starter; the viable count of the streptococcus thermophilus in the composite bacterial liquid is 2 multiplied by 10 10 CFU/g, viable count of bacillus subtilis is 1.5X10 10 CFU/g。
Application example 1: and (3) preparing the composite bacteria antibiotic-free fermented feed.
The weight ratio of the starter, the brown sugar, the water and the fermentation base material is 0.05:5:10:50, adding a starter, brown sugar and water into the fermentation bed charge, uniformly mixing, performing aerobic fermentation for 6 hours at 20 ℃ and ventilation of 2L/min, and performing anaerobic fermentation for 10 days at 35 ℃ to obtain the composite bacteria antibiotic-free fermented feed.
Application example 2: and (3) preparing the composite bacteria antibiotic-free fermented feed.
The weight ratio of the leavening agent to the brown sugar to the water to the fermentation bed charge is 0.1:24:26:100, adding a starter, brown sugar and water into the fermentation bed charge, uniformly mixing, performing aerobic fermentation for 7h at 22 ℃ and ventilation of 3L/min, and performing anaerobic fermentation for 12 days at 36 ℃ to obtain the composite bacteria antibiotic-free fermented feed.
Application example 3: and (3) preparing the composite bacteria antibiotic-free fermented feed.
The weight ratio of the leavening agent to the brown sugar to the water to the fermentation bed charge is 0.2:50:50:200, adding a starter, brown sugar and water into the fermentation base material, uniformly mixing, performing aerobic fermentation for 8 hours at 25 ℃ and ventilation of 3.5L/min, and performing anaerobic fermentation for 14 days at 38 ℃ to obtain the composite bacteria antibiotic-free fermented feed.
Comparative example 1:
the preparation of the composite bacterial anti-fermentation feed according to the method of application example 1 is characterized in that alfalfa extract and pectase are not added into the fermenting agent, and the specific steps are as follows:
(1) The bacillus subtilis bacterial liquid and the streptococcus thermophilus bacterial liquid are mixed according to the weight ratio of 1:1, mixing the materials in proportion to obtain a composite bacterial liquid; the viable count of the streptococcus thermophilus in the composite bacterial liquid is 1.5x10 10 CFU/g, viable count of bacillus subtilis is 1×10 10 CFU/g。
(2) According to the weight ratio of the composite bacterial liquid to the brown sugar to the water to the fermentation bed charge of 0.05:5:10:50, adding the composite bacterial liquid, brown sugar and water into the fermentation bed charge, uniformly mixing, performing aerobic fermentation for 6 hours at 20 ℃ and ventilation of 2L/min, and performing anaerobic fermentation for 10 days at 35 ℃ to obtain the composite bacterial antibiotic-free fermented feed.
Comparative example 2:
the preparation of the composite bacterial anti-fermentation feed according to the method of application example 1 is different in that alfalfa extract is not added into the starter, and the specific steps are as follows:
(1) The bacillus subtilis bacterial liquid and the streptococcus thermophilus bacterial liquid are mixed according to the weight ratio of 1:1, and then mixing the composite bacterial liquid and pectase according to the weight ratio of 1:1, mixing the materials in proportion to obtain a starter; the viable count of the streptococcus thermophilus in the composite bacterial liquid is 1.5x10 10 CFU/g, viable count of bacillus subtilis is 1×10 10 CFU/g。
(2) The weight ratio of the starter, the brown sugar, the water and the fermentation base material is 0.05:5:10:50, adding a starter, brown sugar and water into the fermentation bed charge, uniformly mixing, performing aerobic fermentation for 6 hours at 20 ℃ and ventilation of 2L/min, and performing anaerobic fermentation for 10 days at 35 ℃ to obtain the composite bacteria antibiotic-free fermented feed.
Comparative example 3:
the preparation of the compound bacteria anti-fermentation feed according to the method of application example 1 is different in that pectase is not added into the ferment, and the specific steps are as follows:
(1) The bacillus subtilis bacterial liquid and the streptococcus thermophilus bacterial liquid are mixed according to the weight ratio of 1:1, and then mixing the composite bacterial liquid and alfalfa extract according to the weight ratio of 1: mixing the materials according to a proportion of 0.5 to obtain a starter; the viable count of the streptococcus thermophilus in the composite bacterial liquid is 1.5x10 10 CFU/g, viable count of bacillus subtilis is 1×10 10 CFU/g。
(2) The weight ratio of the starter, the brown sugar, the water and the fermentation base material is 0.05:5:10:50, adding a starter, brown sugar and water into the fermentation bed charge, uniformly mixing, performing aerobic fermentation for 6 hours at 20 ℃ and ventilation of 2L/min, and performing anaerobic fermentation for 10 days at 35 ℃ to obtain the composite bacteria antibiotic-free fermented feed.
Test example: feeding test of growing and fattening pigs.
(1) The test method comprises the following steps:
and selecting 60 healthy growing-finishing pigs with the body condition close to that of the growing-finishing pigs, numbering from 1 to 60, randomly dividing the growing-finishing pigs into 6 groups of 10 growing-finishing pigs, feeding the growing-finishing pigs in separate houses, and feeding the growing-finishing pigs in the same group into the same pig house. The temperature of each pig house is controlled to be 25 ℃, the relative humidity is controlled to be 70%, other growing environment conditions of each group of pigs are guaranteed to be completely consistent, all growing and fattening pigs are fed three times a day in the morning, in the evening, the feeding amount is 2kg a day, water is freely drunk, the manure is cleaned twice a day, the house is kept clean, and the experiment is carried out for 30 days.
The feeds for groups 1-6 were as follows:
group 1: feeding the composite bacteria antibiotic-free fermented feed prepared in application example 1; group 2: feeding the composite bacteria antibiotic-free fermented feed prepared in application example 2; group 3: feeding the composite bacteria non-antibiotic fermented feed prepared in application example 3; group 4: feeding the composite bacteria antibiotic-free fermented feed prepared in the comparative example 1; group 5: feeding the composite bacteria antibiotic-free fermented feed prepared in the comparative example 2; group 6: the composite bacteria antibiotic-free fermented feed prepared in the comparative example 3 is fed.
Weighing and recording each growing-finishing pig after 30 days, calculating daily gain of each pig in each group of growing-finishing pigs, taking an average value of the results, and calculating feed-meat ratio; then, 2 pigs were slaughtered randomly for each group, and the eye muscle area, intramuscular fat and drip loss were measured, and the results were averaged.
Wherein, the eye muscle area and intramuscular fat are measured by the method described in the paper of alfalfa on the expression of genes related to pig physiology and meat quality, and the drip loss is measured by the method described in the paper of three additives on the production performance of fattening pigs and the influence of meat quality on intestinal microorganisms.
(2) Test results:
table: meat quality and feed ratio data of 1-6 groups
As shown in the table, compared with the 4-6 groups, the data of the eye muscle area and intramuscular fat in the data of the 1-3 groups are larger, the data of feed conversion ratio and drip loss are smaller, and the results show that the composite bacteria anti-fermentation feed prepared by feeding the application examples 1-3 can effectively improve the pork quality of growing and fattening pigs and has better feed effect.
Meanwhile, the feed of the 4 th group is prepared by fermenting the compound bacterial liquid in the comparative example 1, the feed of the 5 th group is prepared by fermenting the compound bacterial liquid in the comparative example 2 and pectase in a compounding way, the feed of the 6 th group is prepared by fermenting the compound bacterial liquid in the comparative example 3 and the alfalfa extract in a compounding way, and the 1 st group and the 4 th-6 th groups are compared with each other, so that the synergistic effect of improving the feed effect is achieved by compounding the compound bacterial liquid, the alfalfa extract and the pectase used in the application.
The above description is only of the preferred embodiments of the present application and is not intended to limit the present application, but various modifications and variations can be made to the present application by those skilled in the art. Any modification, equivalent replacement, improvement, etc. made within the spirit and principle of the present application should be included in the protection scope of the present application.
Claims (5)
1. The complex bacterial enzyme biological starter is characterized by comprising complex bacterial liquid, alfalfa extract and pectinase according to the weight ratio of 1: (0.5-2): mixing the components (1-3); the composite bacterial liquid is prepared from bacillus subtilis and streptococcus thermophilus according to the weight ratio of 1:1, and is compounded according to the proportion;
the strain number of the bacillus subtilis is CCTCC AB 130010, and the strain number of the streptococcus thermophilus is CCTCC AB 2010206;
the alfalfa extract is prepared by the following method:
drying and pulverizing herba Medicaginis, adding 10 times of ethanol solution with volume fraction of 60% into pulverized herba Medicaginis, reflux extracting for 2 hr, recovering ethanol from the extractive solution, adding aluminum oxide to adsorb impurities, filtering, collecting filtrate, and spray drying the filtrate to obtain herba Medicaginis extract.
2. A complex bacterial enzyme according to claim 1The object ferment is characterized in that the viable count of streptococcus thermophilus in the composite bacterial liquid is (1.5-2) multiplied by 10 10 CFU/g, the viable count of bacillus subtilis is (1-1.5). Times.10 10 CFU/g。
3. Use of a complex bacterial enzyme biological starter according to any one of claims 1-2 for the preparation of a complex bacterial antibiotic-free fermented feed.
4. The use according to claim 3, wherein the complex bacteria enzyme starter, brown sugar and water are added into the fermentation base material, and the mixture is uniformly mixed, and the mixture is subjected to aerobic fermentation for 6-8 hours and anaerobic fermentation for 10-14 days to prepare the complex bacteria antibiotic-free fermented feed;
the fermentation bed charge consists of the following raw materials in parts by weight: 60 parts of corn flour, 24 parts of bean pulp, 10 parts of bran, 18 parts of corncob, 2 parts of molasses, 5 parts of rice bran, 1 part of ammonium sulfate and 5 parts of stone powder;
the weight ratio of the complex bacterial enzyme starter, the brown sugar, the water and the fermentation bed charge is (0.05-0.2): (5-50): (10-50): (50-200).
5. The use according to claim 4, wherein the aerobic fermentation conditions are: the anaerobic fermentation conditions are that the temperature is 20-25 ℃, the ventilation rate is 2-3.5L/min: sealing and fermenting at 35-38deg.C.
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Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20150080983A (en) * | 2014-01-02 | 2015-07-13 | 고려대학교 산학협력단 | Fermented Castanea crenata inner shell extracts for anti-obesity and manufacturing method thereof |
CN104938784A (en) * | 2015-06-26 | 2015-09-30 | 绥化学院 | Method for preparing animal probiotics fodder by fermenting edible mushroom waste, straw and pasture |
CN110432294A (en) * | 2019-08-26 | 2019-11-12 | 厦门市民安创享实业有限公司 | A kind of bacteriostatic agent of biofermentation, preparation method and application |
WO2020058223A1 (en) * | 2018-09-17 | 2020-03-26 | Dsm Ip Assets B.V. | Animal feed composition and use thereof |
CN112136974A (en) * | 2020-09-28 | 2020-12-29 | 山东胜伟盐碱地科技有限公司 | Livestock feed and preparation method thereof |
CN114052116A (en) * | 2022-01-18 | 2022-02-18 | 山东健源生物科技有限公司 | Probiotic plant extract compound biological agent and preparation method and application thereof |
WO2022081947A1 (en) * | 2020-10-16 | 2022-04-21 | Dupont Nutrition Biosciences | Feed compositions for animal health |
-
2023
- 2023-08-03 CN CN202310966499.0A patent/CN116686903B/en active Active
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20150080983A (en) * | 2014-01-02 | 2015-07-13 | 고려대학교 산학협력단 | Fermented Castanea crenata inner shell extracts for anti-obesity and manufacturing method thereof |
CN104938784A (en) * | 2015-06-26 | 2015-09-30 | 绥化学院 | Method for preparing animal probiotics fodder by fermenting edible mushroom waste, straw and pasture |
WO2020058223A1 (en) * | 2018-09-17 | 2020-03-26 | Dsm Ip Assets B.V. | Animal feed composition and use thereof |
CN110432294A (en) * | 2019-08-26 | 2019-11-12 | 厦门市民安创享实业有限公司 | A kind of bacteriostatic agent of biofermentation, preparation method and application |
CN112136974A (en) * | 2020-09-28 | 2020-12-29 | 山东胜伟盐碱地科技有限公司 | Livestock feed and preparation method thereof |
WO2022081947A1 (en) * | 2020-10-16 | 2022-04-21 | Dupont Nutrition Biosciences | Feed compositions for animal health |
CN114052116A (en) * | 2022-01-18 | 2022-02-18 | 山东健源生物科技有限公司 | Probiotic plant extract compound biological agent and preparation method and application thereof |
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