Convenient observation method of orchid mycorrhiza microstructure
A microstructure and plant root technology, applied in the agricultural field, can solve the problems of complex and cumbersome, poor observation effect, long time-consuming, etc., and achieve the effect of convenient and fast operation, good observation effect and reliable results
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0025] Example 1 Isolation and identification of orchid mycorrhizal fungi:
[0026] 1. Separation of root materials: Take the potted Chunlan from Shanghai Academy of Agricultural Sciences and move it to a shaded greenhouse for later use.
[0027] 2. Separation and identification medium:
[0028] Use malt extract medium (MEA), the formula is: malt extract 20g, tryptone 1g, glucose 20g, agar 20g, distilled water to 1000ml, then autoclave at 121°C for 20 minutes, cool to 60 When the temperature is below 0.03 g streptomycin is added.
[0029] 3. Separation and morphological identification methods:
[0030] Isolation of mycorrhizal fungal strains: take several sections of roots of fresh and healthy orchid plants, rinse them under tap water until there is no sludge on the surface of the roots. Cut the roots into several small sections about 10cm long, wash them three times with sterile water, soak the filter paper in 75% alcohol for 60s, then immerse in 2% sodium hypochlorite for...
Embodiment 2
[0044] Example 2 Screening of suitable dyeing methods
[0045] Take out the orchid tissue culture seedlings, cut off the 3-6 cm long roots with a blade, rinse them with deionized water, blot the water and fix them in FAA fixative solution for more than 24 hours. Prepare a petri dish containing deionized water, make freehand slices of the fixed roots, the thickness of the slices is less than 1cm, pick thinner slices with uniform thickness and put them into the collection tube, immerse in 10% KOH solution, choose 10% KOH Different time gradients for dissociation of the dissociation solution, specifically 5min, 10min, 30min and 60min. Then place them in a 90°C water bath for 10 minutes, pour off the hydrolyzate, add 2% trypan blue staining solution, place them at room temperature and immerse them in different time gradients, specifically 6h, 12h and 24h, and put the experimental materials Put it into a glass slide, drip a drop of glycerin, cover with a cover glass at an angle of...
Embodiment 3
[0050] 1. Orchid tissue culture seedling materials: collect tissue culture seedlings of orchid "Red Beauty", the selected tissue culture seedlings are basically the same, with a fresh weight of about 0.6g and a plant height of about 8cm.
[0051] 2. Cultivation substrate: choose peat that is fully sterilized and dried: yellow sand mixed in a certain proportion as the cultivation substrate, the specific formula is peat: yellow sand 1:2, pour MMN liquid medium, 500mL / 1500g cultivation substrate, mix After uniformity, it is divided into 640mL cultivation flats, autoclaved and cooled to room temperature.
[0052] 3. Inoculation method: transplant 3 orchid seedlings per bottle under aseptic conditions, inoculate 6 bottles of orchid seedlings for each treatment as a repetition, and place them in the tissue culture room for aseptic culture. After one week of growth, check for contamination, and inoculate the strains to be tested in non-polluted tissue culture bottles, that is, place ...
PUM
Property | Measurement | Unit |
---|---|---|
Thickness | 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