Novel microbial strain for pholiota and artificial cultivation method and application of novel microbial strain
A technology of artificial cultivation and parasol, applied in the directions of botanical equipment and methods, microorganism-based methods, biochemical equipment and methods, etc., can solve problems such as unfavorable taxonomy and development of the genus Cymbidium, and achieve a significant inhibition rate and a strong inhibition rate. , nutrient-rich effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0072] Embodiment 1: New strain identification
[0073] On March 22, 2014, Hu Huiping, Liu Yuanchao and others conducted large-scale fungal resource collection and investigation in Chebaling National Nature Reserve, Guangdong. figure 1 as shown, figure 2 and image 3 Its microstructure diagram, and the original strain obtained from tissue isolation, named Pholiota sp. HMGIM-W140054, was preserved in the China Center for Type Culture Collection (CCTCC for short, address For: Wuhan, China), the deposit number is CCTCC NO: M 2019414.
[0074] Since there was no species of the genus Phytophthora consistent with its description in terms of macroscopic and microscopic morphology, in order to further confirm its classification, its DNA was extracted and its multi-segment genes were sequenced, including the fungal ribosomal intergenic region ITS, ribosomal large subunit The base LSU, encoding the second largest subunit rpb2 of RNA polymerase II, etc. are multigene fragments used i...
Embodiment 2
[0088] Embodiment 2 artificial cultivation
[0089] One, culture medium (by weight percentage):
[0090] 1. Tissue separation medium (comprehensive PDA):
[0091] Potato 20%, glucose 2%, agar 2%, potassium dihydrogen phosphate 0.3%, magnesium sulfate 0.15%, vitamin B1 trace, and the rest is water.
[0092] 2. Purified mother seed medium (Red Bengal medium):
[0093] 0.5% peptone, 1% glucose, 0.1% potassium dihydrogen phosphate, magnesium sulfate (MgSO4 7H 2 O) 0.05%, agar 2%, 1 / 3000 Bengal red solution 10%, chloramphenicol 0.01%, and the rest is water.
[0094] 3. Production medium of mother species (enriched with comprehensive PDA):
[0095] Potato 20%, glucose 2%, peptone 1%, agar 2%, potassium dihydrogen phosphate 0.3%, magnesium sulfate 0.15%, vitamin B1 trace, and the rest is water.
[0096] 4. Production medium:
[0097] 98-99% sorghum, 1-2% calcium carbonate.
[0098] 5. Cultivation material:
[0099] 31% cottonseed hulls, 58% wood chips, 10% bran, 1% CaCO 3 ;T...
Embodiment 3
[0125] Embodiment 3 fermented liquid antibacterial activity assay
[0126] 1. Method
[0127] 1. Preparation:
[0128] Culture medium for bacteria: nutrient agar / broth medium;
[0129] Nutrient agar / broth medium: beef extract 3g, peptone 10g, sodium chloride 5g, agar 15g, add water to 1000ml to adjust pH to 7.4 (no agar in nutrient broth).
[0130] The preparation of test sample ethyl acetate extract: use rice culture medium (prescription is rice+water), insert bacterial strain of the present invention and cultivate for 45 days, add ethyl acetate, ultrasonic extraction 2 times, 40min / time, merge extract , recover the solvent in a rotary evaporator, and transfer it to a collection bottle when the extract is about 1-2 mL by rotary evaporation, and place the ethyl acetate extract in a vacuum desiccator. Sterilize with a sterile syringe and a membrane filter for use.
[0131] Positive control preparation: ampicillin cryopreservation solution, diluted with sterile water to a re...
PUM
Property | Measurement | Unit |
---|---|---|
diameter | 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