Microbial live bacterium agent, preparation method and application thereof
A technology of live bacteria preparation and microorganism, applied in the field of microorganism preparation, can solve problems such as being unfavorable to human health, unable to guarantee vitality, and reducing the number of live bacteria, and achieve the effects of comprehensive health care efficacy, low cost and wide applicability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0024] Preparation of live lactic acid bacteria preparation:
[0025] Take the prepared bacterial cellulose membrane (also commercially available), cut it into 5 × 5mm cubic particles, sterilize and set aside;
[0026] Take 10g of peptone, 10g of beef extract, 5g of yeast extract, 20g of glucose, 801ml of Tween, 2g of diammonium hydrogen citrate, 5g of sodium acetate, 2g of dipotassium hydrogen phosphate, MnSO 4 ·7H 2 O0.05g, MgSO 4 ·7H 2 O 0.2g, calcium carbonate 20g, agar 20g, distilled water 1L to prepare the culture medium, adjust the pH to 6.8 with NaOH, and sterilize.
[0027] Add the above-mentioned bacterial cellulose particles into the culture medium in a volume ratio of 30:100, and stir and mix;
[0028] Inoculate Lactobacillus bulgaricus and culture at 37°C for 12 hours;
[0029] Remove bacterial cellulose particles under aseptic conditions and wash with sterile distilled water;
[0030] Use a freeze dryer to freeze-dry for 12 hours at -40 ° C and a vacuum of ...
Embodiment 2
[0033] Preparation of live bifidobacterium preparations:
[0034] Take the prepared bacterial cellulose membrane, cut it into 3 × 3mm cubic particles, sterilize and set aside;
[0035] Get commercially available bifidobacterium BS culture medium (Shanghai Hufeng Biotechnology Co., Ltd.), and sterilize;
[0036] Add the above-mentioned bacterial cellulose particles into the culture medium in a volume ratio of 50:100, and stir and mix;
[0037] Inoculate Bifidobacterium bifidum, culture at 37°C for 10 hours;
[0038] Remove bacterial cellulose particles under aseptic conditions and wash with sterile distilled water;
[0039] Pre-cool at -10°C for 15 minutes;
[0040] Use a freeze dryer to freeze-dry for 8 hours at -80°C and a vacuum of 40Pa;
[0041] Pulverize and pack aseptically to obtain a powdered live bifidobacterium preparation.
Embodiment 3
[0043] Preparation of live yeast preparations:
[0044] Take the prepared bacterial cellulose membrane, cut it into 8×8mm cubic particles, sterilize and set aside;
[0045] Get commercially available yeast YPD medium (Shanghai Jiemei Gene Pharmaceutical Technology Co., Ltd.), and sterilize;
[0046] Add the above-mentioned bacterial cellulose particles into the culture medium in a volume ratio of 70:100, and stir and mix;
[0047] Inoculate Saccharomyces cerevisiae and culture at 27°C for 5 hours;
[0048] Remove bacterial cellulose particles under aseptic conditions and wash with sterile distilled water;
[0049] Pre-cool at -20°C for 8 minutes;
[0050]Use a freeze dryer to freeze-dry for 7 hours at -100°C and a vacuum of 60Pa;
[0051] Pulverize and pack aseptically to obtain a powdered live yeast preparation.
[0052] Detection:
[0053] The live bacterial preparations in Examples 1-3 were respectively taken and stored at 4°C. Determination of the number of live bac...
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