Method for preparing edible fungus circulating cultivation stuff by utilizing waste bacteria bran
A technology of discarded fungi and edible fungi, applied in the field of edible fungus cultivation materials, can solve the problems of inability to utilize nutrients, inability to eliminate harmful metabolites polluting microorganisms, and affecting cultivation effects, so as to improve the secondary utilization rate and increase the degree of enzymatic hydrolysis , considerable economic benefits
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0018] First remove the plastic bag film outside the discarded bacteria bag, and crush the bacteria group into pieces, then put it into the steam flash tank, and feed steam to make the steam pressure rise to 0.1Mpa. After maintaining for 30 minutes, Then the pressure is raised to 1.0Mpa, and immediately exhausted and decompressed to normal pressure, the bacteria block is taken out and dried, and further crushed into fine pieces; by weight, add 5 1 part of microbial enzyme inoculated with Trichoderma and 60 parts of water were mixed well, and kept at 30°C for 6 hours for microbial enzymolysis; 20 parts of wheat bran and 0.05 part of potassium dihydrogen phosphate were added to the bacterial block after microbial enzymatic hydrolysis , 0.01 part of magnesium sulfate, 0.5 part of calcium sulfate, 0.001 part of zinc sulfate and 50 parts of water, mix well, and finally dry or sun-dry the compounded bacteria block until the water content is less than 12%, which can be used as edible ...
Embodiment 2
[0020] First remove the plastic bag film outside the discarded bacteria bag, and crush the bacteria group into pieces, then put it into the steam flash tank, and feed steam to make the steam pressure rise to 0.3Mpa. After maintaining for 10 minutes, Then the pressure is raised to 0.6Mpa, and immediately exhausted and decompressed to normal pressure, the bacteria block is taken out and dried, and further crushed into fine pieces; by weight, add 8 1 part of microbial enzyme inoculated with Trichoderma and 80 parts of water were mixed well, and incubated at 32°C for 8 hours for microbial enzymolysis; 15 parts of rice bran and 0.2 part of potassium dihydrogen phosphate were added to the bacterial block after microbial enzymolysis, Mix 0.05 parts of magnesium sulfate, 1 part of calcium sulfate, 0.002 parts of zinc sulfate and 50 parts of water, mix well, and finally dry or sun-dry the compounded bacteria blocks until the moisture content is less than 12%, then they can be used as ed...
Embodiment 3
[0022] First remove the plastic bag film outside the discarded bacteria bag, and crush the bacteria group into pieces, then put it into the steam flash tank, and feed steam to make the steam pressure rise to 0.2Mpa. After maintaining for 15 minutes, Then the pressure is raised to 0.4Mpa, and immediately exhausted and decompressed to normal pressure, the bacteria block is taken out and dried, and further crushed into fine pieces; by weight, add 10 Mix 100 parts of microbial enzyme inoculated with Aspergillus oryzae and 100 parts of water, and incubate at 35°C for 10 hours for microbial enzymolysis; add 5 parts of wheat bran and 0.1 part of potassium dihydrogen phosphate to the bacterial block after microbial enzymolysis , 0.02 parts of magnesium sulfate, 1 part of calcium sulfate, 0.004 parts of zinc sulfate and 40 parts of water are compounded, mixed well, and finally the compounded bacteria block is dried or dried until the water content is less than 12%, which can be used as ...
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