Trichoderma koningiopsis and application thereof in prevention and treatment of litchi anthracnose
A technology of Trichoderma pseudocorningi and microbial strains, applied in the direction of application, fungicides, fungi, etc., can solve the problems of pesticide residue environment, increase of drug resistance of pathogenic bacteria, even drug resistance, pollution, etc., and achieve wide adaptability and good Development and application prospects, the effect of little impact on the ecological environment
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0025] Embodiment 1: Isolation, purification and preservation of Trichoderma pseudokoningeni
[0026] (1) Preparation of PDA medium: first wash and peel the potatoes, then weigh 200g of potatoes, chop them into a pot, add 800mL of water to boil for 0.5h, filter with eight layers of gauze, then add 20g of glucose, add water Dilute to 1000mL, stir and mix with a glass rod, add 15g of agar, fully heat and dissolve, then dispense into 250mL Erlenmeyer flasks, sterilize with damp heat at 121°C for 20min, and store for later use.
[0027] (2) Trichoderma strain samples were isolated from the green mold layer on the litchi litchi leaves in the Litchi Base of the College of Horticulture, South China Agricultural University. The strains were isolated and purified with reference to the method of Fang Zhongda et al., and slightly modified: use inoculation Pick a little green mold layer on the PDA medium plate with a needle, place it in an incubator at 28°C and cultivate it. After the gre...
Embodiment 2
[0032] Embodiment 2: confrontation culture method measures the activity of Trichoderma pseudokoningeni
[0033] (1) The preparation of PDA medium is the same as in Example 1.
[0034] (2) Preparation of single colony and bacterial plate of Trichoderma pseudocornifolia: pick Trichoderma pseudocorniensis hyphae on a PDA medium plate with a sterilized toothpick, and culture at 28°C for 3-4 days to obtain a single colony; The edge of Trichoderma pseudoconingi colony is punched to obtain a round fungus disc.
[0035] (3) Cultivation of litchi anthracnose bacteria and preparation of bacteria plates: inoculate the litchi anthrax strains stored at -20°C on a PDA medium plate for activation, and punch them with a puncher with a diameter of 5 mm after the colonies cover the plate Take the edge of the colony to obtain a round disk.
[0036] (4) Activity measurement: on the PDA plate culture medium of 9cm, insert the Trichoderma pseudocornibacterium dish that step (2) prepares and the l...
Embodiment 3
[0038] Embodiment 3: growth rate method measures the activity of Trichoderma pseudokoningenii biological preparation
[0039] (1) The preparation of PDA medium is the same as Example 1; the preparation of PDB liquid medium is except adding agar, and other is identical with the formula of PDA solid medium, and after the medicament weighed is fully dissolved, be subpackaged in conical flasks (each Fill the bottle with 100mL culture solution), stopper, bandage, sterilize with damp heat at 121°C for 20min, cool and store for later use.
[0040] (2) Preparation of Trichoderma pseudocorningii aseptic fermentation filtrate (biological agent): take the Trichoderma pseudocorningii bacteria plate prepared in step (2) of Example 2 and insert into step (1) to prepare the PDB nutrient solution equipped with 100mL Place in a Erlenmeyer flask at 28°C with a shaker speed of 180rpm and shake in the dark for 5 days, then centrifuge at 5000rpm for 10min, absorb the supernatant, and filter out th...
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