Feed-use high-activity lactobacillus solid preparation and preparation method thereof
A lactic acid bacteria, high activity technology, applied in the field of feed high activity lactic acid bacteria solid preparation and its preparation, microbial feed additives, can solve the problems of poor repeatability and stability, reduced biological activity, single preparation formula, etc., to achieve stable morphological structure , The effect of reducing the ratio of feed to meat and the number of intestinal villi
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0041] (1) Preparation of plant extracts
[0042] Dry 1 to 10 parts of eucommia leaves, tangerine peel and licorice at 40°C to 55°C until the moisture content is ≤10%, crush them to 60 to 80 mesh, extract 10 to 50 parts of absolute ethanol for 1 to 3 hours, and filter. Rotary evaporation to obtain the extract (density 0.7 ~ 1.5g / cm 3 ), by adding 10 to 200 parts of water.
[0043] (2) Preparation of MRS medium and optimal medium
[0044] The preparation of MRS medium: take peptone 1% (W / V), glucose 2% (W / V), beef extract 1% (W / V), anhydrous sodium acetate 0.5% (W / V), yeast extract Ointment 0.5% (W / V), Tween 800.1ml, Dipotassium hydrogen phosphate 0.2% (W / V), Diammonium hydrogen citrate 0.2% (W / V), Magnesium sulfate heptahydrate 0.058% (W / V) , manganese sulfate monohydrate 0.025% (W / V), water 100ml, adjust the pH to 7.0±0.2; use moist heat sterilization, the temperature is 115 ℃, and the sterilization time is 30min.
[0045] The preparation of the preferred medium: 1-4% (W / ...
Embodiment 2
[0074] (1) Preparation of LB medium and preparation of optimal medium
[0075] Preparation of LB medium: take tryptone 1% (W / V), yeast extract 0.5% (W / V), sodium chloride 1% (W / V), water 100ml, pH7.0±0.2; Sterilization, 121°C, 20min.
[0076] The preparation of the preferred medium: 1-4% (W / V) of sucrose, 1-3% (W / V) of corn steep liquor, 0.4-2% (W / V) of yeast extract, 0.06-0.1% (W / V) of magnesium chloride ), manganese sulfate 0.04-0.2% (W / V), calcium carbonate 0.1-0.4% (W / V), sodium chloride 0.2-0.6% (W / V), water 100ml, pH7.0±0.2; Sterilize, the temperature is 115°C, and the sterilization time is 30min.
[0077] (2) Preparation of bacteria slime
[0078] a. Enterococcus faecalis (ATCC19433) was selected, and the strain was cultured in LB medium at 35°C for 8 hours to obtain a first-grade seed liquid;
[0079] b. Put the primary seed liquid into the seed tank according to the inoculum amount of 2% to expand the cultivation, and cultivate it in LB medium for 6 hours under mi...
Embodiment 3
[0109] (1) Prepare culture medium
[0110] Prepare LB medium: take tryptone 1% (W / V), yeast extract 0.5% (W / V), sodium chloride 1% (W / V), water 100ml, pH7.0±0.2; Sterilization, 121°C, 20min.
[0111] Prepare optimal medium: sucrose 1-4% (W / V), corn steep liquor 1-3% (W / V), yeast extract 0.4-2% (W / V), magnesium chloride 0.06-0.1% (W / V) , manganese sulfate 0.04-0.2% (W / V), calcium carbonate 0.1-0.4% (W / V), sodium chloride 0.2-0.6% (W / V), water 100ml, pH7.0±0.2; sterilization method : Moist heat sterilization, 115°C, 30min.
[0112] (2) Preparation of bacteria slime
[0113] a. Select Lactobacillus lactis (ATCC12315), Bacillus bulgaricus (ATCC11842) and Enterococcus lactis (ATCC19435), and culture the strains in LB medium under microaerobic conditions (ie 0.3mg / L dissolved oxygen) at 35°C 8h, obtain the primary seed liquid of three kinds of bacteria;
[0114] b. Put the first-level seed liquid of the three bacteria into the seed tank according to the inoculum amount of 2% to...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com