Trichoderma koningiopsis Hk37 strain, biocontrol inoculant, and preparation method of biocontrol inoculant and application of Trichoderma koningiopsis Hk37 strain and biocontrol inoculant
A technology of Trichoderma pseudocorning and biocontrol agent, which can be applied to biochemical equipment and methods, microorganism-based methods, and botanical equipment and methods, etc., and can solve problems such as increased cost and hidden dangers in food safety.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0041] The present invention also provides a preparation method of the above-mentioned biocontrol agent, comprising the following steps:
[0042] The above-mentioned Hk37 bacterial strain is inoculated in PDA medium, and cultivated for 7-10 days to obtain the biocontrol agent.
[0043] Unless otherwise specified, the present invention has no special requirements on the source of each component of the PDA medium, and commercially available products well known to those skilled in the art can be used.
[0044] In the present invention, in 1 L, the PDA medium preferably includes: 200 g of potatoes, 20 g of glucose, 20 g of agar and the remainder of water; the water preferably includes distilled water; the pH of the PDA medium is preferably 7.0.
[0045] In the present invention, the culture time is 7-10 days, preferably 8-9 days, more preferably 8.5 days; the culture temperature is preferably 20-30°C, more preferably 25°C.
[0046] The present invention also provides the applicat...
Embodiment 1
[0051] Isolation and identification of strains
[0052] Where and how the strain was isolated:
[0053] Collect the swollen rapeseed root tissue of the rape clubroot disease-infected field in Zhijiang City, Hubei Province, soak it in 75% ethanol (volume concentration) for 2 to 3 minutes, wash it with sterile water for 5 to 6 times, remove the root epidermis, and then cut the root Inoculate into small pieces, inoculate on PDA medium, and incubate upside down in a constant temperature culture room at 20°C for 2 to 3 days. After the tissue is covered with hyphae, use an inoculation needle to pick out mycelia in a new PDA medium, and culture for 2 ~ 3 days, repeat the purification of mycelium tips 3 ~ 4 times, obtain a fungal strain and number it as Hk37; the preparation of the PDA medium is as follows: take 200g of potatoes, 20g of glucose, 20g of agar, add distilled water to 1000mL and mix evenly , adjust the pH to 7.0, and sterilize with high pressure steam at 121° C. for 20 m...
Embodiment 2
[0062] A biocontrol agent, the preparation method of which is:
[0063] The bacterial strain purified in Example 1 was inoculated into PDA medium (the preparation method of the medium was the same as Example 1) for activation, cultivated in a constant temperature culture room at 25°C for 8 days, and used sterile ddH 2 O the conidia are washed down, and the eluate is collected to be the spore suspension of the Hk37 strain. Adjust the concentration of conidia to about 10 7 spores / mL to obtain the biocontrol agent.
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com



