Method for preparing erythritol with bean dregs as main raw material
A main raw material, a technology for erythritol, applied in the field of preparing erythritol, can solve the problems of difficulty in realizing full hydrolysis and utilization of bean dregs, high protein content, high carbon-nitrogen ratio, and inability to hydrolyze bean dregs cellulose, etc. Synthetic, Nutritious, Inexpensive Effects
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0025] 1. After the bean dregs are dried and dehydrated, the moisture content is controlled at 60% by adding distilled water. According to the inoculum size is 1×10 8 cells / 100g dry bean dregs A. elegans The spores are mixed well, fermented at 30°C for 5 days, sterilized at 115°C for 30 minutes after pre-fermentation, and dried at 60°C.
[0026] 2. The amount of pre-fermented dried okara is 30.0 g / L, and potassium chloride is used as the osmotic pressure regulator, and the added concentration is 20 g / L. The inoculum size is 1×10 6 cells / liter medium; culture temperature 26°C; stirring speed 140 rpm; pH was not adjusted during the fermentation process. The yield of erythritol was determined to be 0.41 g / g pre-fermented okara.
Embodiment 2
[0028] 1. After the bean dregs are dried and dehydrated, the moisture content is controlled at 30% by adding distilled water. According to the inoculum size is 1×10 5 cells / 100g dry bean dregs A. elegans The spores are mixed well, fermented at 26°C for 3 days, sterilized at 115°C for 30 minutes after pre-fermentation, and dried at 60°C.
[0029] 2. The amount of pre-fermented dried bean dregs was 30.0 g / L, and sodium chloride was used as an osmotic pressure regulator at a concentration of 40 g / L; the inoculation amount was 1×10 8 cells / liter of medium Y. lipolytica Cell concentration; culture temperature 30°C; stirring speed 200 rpm; pH was always controlled at 3.0 during the fermentation process. The yield of erythritol was determined to be 0.30 g / g pre-fermented okara.
Embodiment 3
[0031] 1. After the bean dregs are dried and dehydrated, the moisture content is controlled at 30% by adding distilled water. According to the inoculum size is 1×10 5 Cells per 100 grams of dried bean dregs A. elegans The spores are mixed well, fermented at 26°C for 3 days, sterilized at 115°C for 30 minutes after pre-fermentation, and dried at 60°C.
[0032] 2. The amount of pre-fermented dried bean dregs was 30.0 g / L, and sodium chloride was used as an osmotic pressure regulator at a concentration of 40 g / L; the inoculation amount was 1×108 cells per liter of medium Y. lipolytica Cell concentration; culture temperature 30°C; stirring speed 200 rpm; pH was adjusted to 3.0 48 hours before fermentation, and adjusted to pH 5.0 after 48 hours. The yield of erythritol was determined to be 0.39 g / g pre-fermented okara.
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