Method for preparing theabrownin and low-molecular-weight tea polysaccharides by fermenting green tea as raw material
A low-molecular-weight, tea polysaccharide technology, which is applied in the deep processing of tea and in the field of food biology, can solve the problems of unfavorable organism absorption and functional activity, limit the application of tea polysaccharides, and unstable solution system, etc., and achieve green energy saving, low price, and No harmful solvent residue effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0016] (1) Use a food grinder to pulverize 500 kg of fried green tea harvested in mid-June, and spray water containing activated Aspergillus niger and Trametes trichotillobacter into the green tea scraps. 5%, that is, 25 kilograms, the number of live bacteria of Aspergillus niger in each liter of bacteria liquid is 8.3×10 7 , the number of live bacteria of Trametes trichotillotype was 7×10 6 First, stir the bacterial liquid and green tea scraps evenly, and ferment for 110 hours at a room temperature of 25°C.
[0017] (2) Add water 70 times its mass to the fermented material in step (1), and heat to 95°C for leaching for 40 minutes. The extract is filtered through gauze and microfiltration membrane to obtain the filtrate.
[0018] (3) The filtrate in step (2) is concentrated to 1 / 2 of the original volume by thermal evaporation, then add 6 times the volume concentration of 70% food grade alcohol aqueous solution to the concentrated solution, mix well, let stand, centrifuge, Co...
Embodiment 2
[0023] (1) Grind 1000 kg of baked green tea harvested in early September with a food grinder, and spray water containing activated Aspergillus niger and Trametes trichotillobacter into the green tea scraps. 20%, namely 200 kilograms, the number of live bacteria of Aspergillus niger in every liter of bacteria liquid is 4.6×10 7 , the viable count of Trametes trichotillotype was 4.3×10 6 First, stir the bacterial liquid and green tea scraps evenly, and ferment at 30°C for 72 hours.
[0024] (2) Add 38 times the mass of water to the fermented material in step (1), heat it to 80°C and extract for 120 minutes, and filter the extract through gauze and microfiltration membrane to obtain the filtrate.
[0025] (3) The filtrate in step (2) is concentrated to 1 / 5 of the original volume by vacuum decompression, then add 4 times the volume concentration of 85% food grade alcohol aqueous solution to the concentrated solution, mix well, let stand, and centrifuge , and the supernatant and ...
Embodiment 3
[0030] (1) Use a food grinder to crush 100 kg of steamed green tea harvested in mid-April, and spray water containing activated Aspergillus niger and Trametes trichotillobacter into the green tea scraps. 35%, or 35 kilograms. The number of live bacteria of Aspergillus niger per liter of bacterial liquid was 1.2×10 7 , the viable count of Trametes trichotillotype was 2.1×10 6 First, stir the bacterial liquid and green tea scraps evenly, and ferment for 120 hours at a room temperature of 38°C.
[0031] (2) Add 8 times the mass of water to the fermented material in step (1), heat to 68°C and extract for 220 minutes, and filter the extract through gauze and microfiltration membrane to obtain the filtrate.
[0032] (3) The filtrate in step (2) is concentrated to 1 / 9 of the original volume by thermal evaporation, and then 2.5 times the volume concentration of 95% food-grade alcohol aqueous solution is added to the concentrated solution, fully mixed, left to stand, centrifuged, Co...
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