Method for production of succinic acid
A technology of succinic acid and organic raw materials, applied in recombinant DNA technology, fermentation and other directions
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0054] 2. The preparation method of succinic acid
[0055] The method for producing succinic acid according to the present invention is characterized in that succinic acid is generated by reacting the bacterial cells obtained by culturing the above-mentioned bacteria or their processed product with the organic raw material in a reaction liquid containing the organic raw material, and collecting the succinic acid.
[0056] When the above-mentioned bacteria are used for the production of succinic acid, the bacteria cultured on a slant surface with a solid medium such as agar medium can be directly used for the reaction, but it is preferable to use the above-mentioned bacteria cultured in a liquid medium in advance (seed culture). obtained bacteria. As a medium used for seed culture, a common medium used for bacterial culture can be used. For example, a general medium obtained by adding natural nutrient sources such as meat extract, yeast extract, and peptone to a composition co...
Embodiment 1
[0088] Evaluation in Fermenter - 1
[0089]
[0090] 100mL culture medium (urea: 4g, ammonium sulfate: 14g, potassium dihydrogen phosphate: 0.5g, dipotassium hydrogen phosphate: 0.5g, magnesium sulfate heptahydrate: 0.5g, ferrous sulfate heptahydrate: 20mg, manganese sulfate Hydrate: 20mg, D-biotin: 200μg, thiamine hydrochloride: 200μg, yeast extract: 5g, casein hydrolyzate: 5g, and distilled water: 1000mL) into a 500mL Erlenmeyer flask, at 120°C Heat sterilize for 20 minutes. Cool it to room temperature, and add 4 mL of 50% glucose aqueous solution that has been sterilized in advance, inoculate the Brevibacterium flavum MJ233 / PC-4 / ΔLDH or MJ233 / ΔLDH constructed above, and seed at 30°C for 16 hours. to cultivate.
[0091]
[0092]Mix 365mL culture medium (ammonium sulfate: 1.0g, potassium dihydrogen phosphate: 1.5g, dipotassium hydrogen phosphate: 1.5g, potassium chloride: 1.67g, magnesium sulfate heptahydrate: 0.5g, ferrous sulfate heptahydrate: 40 mg, manganese sulfat...
Embodiment 2
[0100] Evaluation in Fermenter - 2
[0101] For the Brevibacterium flavum MJ233 / PC-4 / ΔLDH strain obtained in the same way as the seed culture of Example 1, under the temperature conditions of 35°C, 36°C, 37°C, 38°C and 39°C, follow the same method as in Example 1 Methods, evaluation of succinic acid production cultures was performed. The relationship between the accumulated concentration of succinic acid and the reaction temperature after 6 hours is as follows image 3 shown.
[0102] Depend on image 3 It can be seen that the succinic acid production efficiency of the MJ233 / PC-4 / ΔLDH strain increases rapidly from 37°C or higher.
PUM
Property | Measurement | Unit |
---|---|---|
absorbance | aaaaa | aaaaa |
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