A kind of tea branch cutting seedling raising stick and seedling raising method
A technology of cutting seedlings and tea branches, which is applied in the field of tea tree breeding, can solve the problems of low survival rate of tea seedlings, inability to ensure effective and timely supply of tea seedlings, and long seedling growth time, so as to avoid fermentation effect, avoid rapid transformation loss, and prevent fermentation fast effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0034] The preparation of embodiment 1 seedling raising stick of the present invention
[0035] Include the following steps:
[0036]Step 1) inactivation of bacteria sticks: choose edible mushroom sticks with a length of 20 cm and a volume of 3.0 L, and inject 400 mL of H2O with a mass ratio of 3.0% from both ends of the unbroken edible mushroom sticks. 2 O 2 The solution was sterilized by high pressure at 120°C for 1-2 hours. After the sterilization was completed, the bacteria sticks were taken out and cooled to 20-25°C at room temperature. Then, 100 mL of alcohol solution with a mass ratio of 15.0% was injected from both ends of the bacteria sticks, and dried at room temperature for 24 hours;
[0037] Step 2) Preparation of fermentation broth: first add 1000g starch to 10kg of pure water, stir evenly, then add bacterial, fungal, and actinomycete microbial fermentation inoculants successively to the starch solution, stir evenly, and seal the solution. Fermentation can take ...
Embodiment 2
[0040] The preparation of embodiment 2 seedling raising stick of the present invention
[0041] Step 1) bacterial stick inactivation: choose the edible fungus fungus bar of length 20cm, volume 3.4L, inject 500mL mass ratio 3.0% H from both ends into the edible fungus fungus bar without broken bag from both ends. 2 O 2 The solution was sterilized by high pressure at 120°C for 1-2 hours. After the sterilization was completed, the bacteria sticks were taken out and cooled to 20-25°C at room temperature. Then, 150 mL of alcohol solution with a mass ratio of 15.0% was injected from both ends of the bacteria sticks, and dried at room temperature for 24 hours;
[0042] Step 2) Preparation of fermentation broth: first add 1000g starch to 10kg of pure water, stir evenly, then add bacterial, fungal, and actinomycete microbial fermentation inoculants successively to the starch solution, stir evenly, and seal the solution. Fermentation can take 3 to 5 days. Among them, 30g of bacterial-...
Embodiment 3
[0045] The preparation of embodiment 3 seedling raising stick of the present invention
[0046] Step 1) bacteria stick inactivation: choose the edible fungus fungus bar of length 20cm, volume 3.6L, inject the edible fungus fungus bar of unbroken bag from both ends into 600mL mass ratio 3.0% H. 2 O 2 The solution was sterilized by high pressure at 120 °C for 1-2 hours. After the sterilization was completed, the bacteria sticks were taken out and cooled to 20-25 °C at room temperature. Then, 200 mL of alcohol solution with a mass ratio of 15.0% was injected from both ends of the bacteria sticks, and dried at room temperature for 24 hours;
[0047] Step 2) Preparation of fermentation broth: first add 1000g starch to 10kg of pure water, stir evenly, then add bacterial, fungal, and actinomycete microbial fermentation inoculants successively to the starch solution, stir evenly, and seal the solution. Fermentation can take 3 to 5 days. Among them, 30 g of bacterial-type fermentatio...
PUM
Property | Measurement | Unit |
---|---|---|
length | 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