Method for producing microbial polysaccharide fermentation broth by using Paenibacillus mucilaginosus
A technology of microbial polysaccharide and Paenibacillus, which is applied in the field of producing microbial polysaccharide fermentation liquid by using Paenibacillus colloid, achieves the effects of improving product grade, short fermentation time and eliminating equipment requirements
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0026] The method for producing microbial polysaccharide fermentation broth by using Paenibacillus mucilaginosus is to inoculate Paenibacillus mucilaginosus ACCC10013 on a medium containing a carbon source and a nitrogen source for fermentation, including the following process steps:
[0027] A. Bacteria heat stimulation
[0028] Under sterile conditions, add the spores of the bacteria in the inclined plane of the test tube to sterile water, shake and wash the spores to make a spore suspension and place it in a sterile container, and place the sterile container containing the spore suspension in boiling water. Heat evenly, take out the aseptic container after 1 minute and cool down rapidly;
[0029] B. Fermentation
[0030] B1. Preparation of culture medium
[0031] Prepare the medium and sterilize it, and cool it to 30°C. The medium consists of the following components in mass percentage:
[0032] Starch 5%, sucrose 5%, ammonium sulfate 0.5%, dipotassium hydrogen phosphate...
Embodiment 2
[0041] In step A in this embodiment, after the aseptic container is evenly heated for 10 minutes, the aseptic container is taken out and rapidly cooled;
[0042] B. Fermentation
[0043] B1. Preparation of culture medium
[0044] Prepare the medium and sterilize it, and cool it to 30°C. The medium consists of the following components in mass percentage:
[0045] Starch 20%, sucrose 10%, ammonium sulfate 5%, dipotassium hydrogen phosphate 20%, magnesium sulfate 10%, ferric chloride 0.5%, calcium carbonate 5%, yeast extract 3%, the balance is sterile water, pH =7.5;
[0046] B2. Cultivate
[0047] Inoculate the strain treated in step A into the culture medium prepared in step B, the fermentation period is 60 hours, the culture temperature is 30°C, and the inoculation amount is the strain: the mass percentage of the culture medium after sterilization is 8%; the air volume is adjusted For: 0-4 hours ventilation ratio is 1: .5VVM, 4-12 hours ventilation ratio is 1: 0.7VVM, 12-2...
Embodiment 3
[0051] In the steps of this embodiment, place the aseptic container in which the spore suspension is housed and heat evenly in boiling water. After 8 minutes, the aseptic container is taken out and rapidly cooled;
[0052]B. Fermentation
[0053] B1. Preparation of culture medium
[0054] Prepare the medium and sterilize it, and cool it to 30°C. The medium consists of the following components in mass percentage:
[0055] Starch 15%, sucrose 8%, ammonium sulfate 3%, dipotassium hydrogen phosphate 15%, magnesium sulfate 8%, ferric chloride 0.3%, calcium carbonate 3%, yeast extract 1%, the balance is sterile water, pH =7.5;
[0056] B2. Cultivate
[0057] Inoculate the strain treated in step A into the culture medium prepared in step B, the fermentation period is 60 hours, the culture temperature is 30°C, and the inoculation amount is the strain: the mass percentage of the culture medium after sterilization is 8%; the air volume is adjusted It is: the ventilation ratio of 0-4...
PUM
![No PUM](https://static-eureka-patsnap-com.libproxy1.nus.edu.sg/ssr/23.2.0/_nuxt/noPUMSmall.5c5f49c7.png)
Abstract
Description
Claims
Application Information
![application no application](https://static-eureka-patsnap-com.libproxy1.nus.edu.sg/ssr/23.2.0/_nuxt/application.06fe782c.png)
- 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