Preparation method and applications of fusarium oxysporum inoculant
A technology of Fusarium oxysporum and inoculum, applied in the field of biopharmaceuticals, can solve the problems of unsuitability for large-scale production, poor root-knot nematode effect, high economic cost, etc., and achieves the effects of low price, reduced dosage, and guaranteed activity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0021] The invention provides a preparation method of Fusarium oxysporum inoculum, the preparation method comprising the following steps:
[0022] (1) Strain cultivation: Purify the non-pathogenic Fusarium oxysporum inside the cucumber root system as the parent fungus, and sterilize the fungus at 121 °C for 20-30 minutes at 25-28 °C Cultivate 3-5 days in the plate culture medium after;
[0023] (2) Fermentation broth preparation: After the liquid medium is sterilized by high pressure and damp heat, add the Fusarium oxysporum cultured in step (1), and then culture it with stirring at a temperature range of 25-28°C for 7-10 days. Obtain the Fusarium oxysporum liquid after culturing as the fermentation liquid;
[0024] (3) Fermentation culture: put the solid medium into the fermentation bottle, and sterilize it at 121°C for 60-90 minutes, then add the fermentation broth generated in step (2), mix well, and Fermentation and cultivation for 7-10 days at a temperature range of 25-...
Embodiment 1
[0037]Embodiment 1: the mycelium of Fusarium oxysporum bacterial strain fus-1 is inoculated on plate medium, and medium formula is PDA medium, and this medium comprises potato 200g, glucose 20g and agar 17g, and configures with distilled water, set up to 1000 mL. After the medium was sterilized at 121°C for 20 minutes, Fusarium Fus-1 was inoculated and cultured at 25°C for 3 days to obtain activated strains.
[0038] The activated fus-1 strain was inoculated into 250 ml Erlenmeyer flasks, each containing 125 ml of PDA liquid medium, and cultured at 25°C for 7 days at a stirring speed of 170 r / min to obtain a large amount of mycelium and Sporulation. The formula of the liquid medium is 200g of potatoes and 20g of glucose, which are prepared with distilled water and adjusted to 1000 mL.
[0039] Put the above fermented liquid into the solid medium, mix well, ferment and cultivate at 25°C for 7 days, the solid medium is covered with white hyphae and spores. The solid medium co...
Embodiment 2
[0041] Embodiment 2: Inoculate the mycelium of Fusarium oxysporum strain fus-1 on the plate culture medium, the medium formula is PDA medium, and this medium comprises potato 200g, glucose 20g and agar 17g, and configures with distilled water, set up to 1000 mL. After the medium was sterilized at 121° C. for 30 minutes, Fusarium Fus-1 was inoculated and cultured at 28° C. for 5 days to obtain activated strains.
[0042] The activated fus-1 strain was inoculated into 250 ml Erlenmeyer flasks, each containing 125 ml of PDA liquid medium, and cultured at 28°C for 10 days at a stirring speed of 220 r / min to obtain a large amount of mycelium and branch Sporulation. The formula of the liquid medium is 200g of potatoes and 20g of glucose, which are prepared with distilled water and adjusted to 1000 mL.
[0043] The fermented liquid propagated by the liquid is added to the solid medium, fully mixed, fermented and cultivated at 28°C for 10 days, and the solid medium is covered with w...
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