Fungal hypha growth test method in gramineous plant stalks
A technology for the growth of gramineous plants and hyphae, which is applied in the direction of biochemical equipment and methods, and the determination/inspection of microorganisms, and can solve the problems of lack of testing methods
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0019] Embodiment 1: Simulated botrytis cinerea causes botrytis cinerea on wheat stalks:
[0020] (1) Take a glass tube with a diameter of 20mm, and open a vent hole every 4mm on the side wall of the glass tube, and control the diameter of the vent hole at 0.2mm;
[0021] (2) Seal the bottom of the glass tube with a filter screen, the filter hole diameter of which is 0.25 mm;
[0022] (3) Pour the glass beads with a diameter of 0.4mm into the glass tube;
[0023] (4) Botrytis cinerea is inoculated on the filter screen at the bottom of the glass tube, then the bottom of the glass tube is put into a petri dish, and the culture solution is poured into the petri dish;
[0024] (5) Put the glass tube together with the culture dish into the culture room for 20 days;
[0025] (6) Observing and recording the growth of Botrytis cinerea mycelium in the glass tube to obtain the growth pattern of Botrytis cinerea mycelium in the wheat stalk.
Embodiment 2
[0026] Embodiment 2: Simulating the fungus to cause the fungus on the bentgrass stalks:
[0027] (1) Take a glass tube with a diameter of 10mm, and open a vent hole every 3mm on the side wall of the glass tube, and control the diameter of the vent hole at 0.1mm;
[0028] (2) Seal the bottom of the glass tube with a filter screen, the filter hole diameter of which is 0.2mm;
[0029] (3) Pour the glass beads with a diameter of 0.4mm into the glass tube;
[0030] (4) Inoculate the mycelia of Mycelia syringae on the filter screen at the bottom of the glass tube, then put the bottom of the glass tube into a petri dish, and pour culture solution into the petri dish;
[0031] (5) Put the glass tube together with the culture dish into the culture room for 14 days;
[0032] (6) Observing and recording the growth of Mycelia mycelia in the glass tube to obtain the growth pattern of Mycelia mycelia in the bentgrass stalk.
Embodiment 3
[0033] Embodiment 3: Simulate the syringa fungus and cause the syringa disease in Echinacea:
[0034] (1) Get a glass tube with a diameter of 50mm, and open a vent hole every 5mm on the side wall of the glass tube, and control the diameter of the vent hole at 0.2mm;
[0035] (2) Seal the bottom of the glass tube with a filter screen, the filter hole diameter of which is 0.3 mm;
[0036] (3) Pour the glass beads with a diameter of 0.5 mm into the glass tube;
[0037] (4) Inoculate the mycelium of the fungus Mycelia syringae on the filter screen at the bottom of the glass tube, then put the bottom of the glass tube into a petri dish, and pour the nutrient solution into the petri dish;
[0038] (5) Put the glass tube together with the culture dish into the culture room for 30 days;
[0039] (6) Observing and recording the growth of Mycelia mycelia in the glass tube, and obtaining the growth pattern of Mycelia mycelia in Elymus stalks.
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