Aspergillus awamori, and microbial inoculant and application thereof
A technology of microbial agent, Aspergillus awamori, which is applied in the field of agricultural microorganisms, can solve the problems of small species and quantity, and achieve the effect of remarkable control effect and less resistance to pesticides
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0030] The isolation and screening of embodiment 1 bacterial classification:
[0031] (1-1) Preparation of PDA medium 、
[0032] The PDA medium: potato 200g, glucose 20g, agar 15-20g, H 2 O 1000ml, pH natural. Wash and peel the potatoes first, then weigh 200g of potatoes and cut them into small pieces, add water to boil (boil for 20-30 minutes), filter with eight layers of gauze, heat, then add agar according to the actual experiment needs, continue to heat and mix well , after the agar is dissolved, add glucose, stir evenly, and then make up water to 1000ml after cooling down a bit, divide into test tubes or Erlenmeyer flasks, stopper, bandage, sterilize at 121°C for about 20 minutes, take out the test tubes and put them on an inclined plane or put them on a flat plate , and store for later use after cooling and solidification.
[0033] The PDA plates and PDA slopes used in the experiment were prepared by conventional operation methods.
[0034] (1-2) Preparation of soi...
Embodiment 2
[0047] Example 2 Screening of cucumber fusarium wilt antagonistic fungi:
[0048] (2-1) Solid medium: prepare PDA medium: same as (1-1) in Example 1.
[0049] (2-2) Activation of Cucumber Fusarium Wilt Pathogenic Bacteria
[0050]Fusarium oxysporum, the pathogenic bacterium of cucumber wilt preserved at low temperature, was inserted into PDA slant medium for activation culture, cultured in an incubator at 28°C for 4 days, and set aside.
[0051] (2-3) Plate antagonism test
[0052] Inoculate the cultured and activated cucumber wilt pathogenic bacteria into the center of the PDA plate, and inoculate the isolated fungi around the plate at the same time, inoculate 4 isolated fungi on each plate, and place them in a fungal incubator at 28°C for cultivation after inoculation. After 48 hours, observe the experimental results every 24 hours, mainly to investigate the presence and size of the inhibition zone. According to the size of the inhibition zone, efficient antagonistic mi...
Embodiment 3
[0053] The preparation of embodiment 3 microbial bacterial agents:
[0054] (3-1) Activation culture of strain 2-17: Inoculate the slant preservation of the isolated Aspergillus awamori (Aspergillus awamori) 2-17 strain on the PDA slant, place it in an incubator at 28°C for 4 days, and then inoculate PDA as the inoculum After inoculation, place the PDA plate in an incubator at 28°C for 4-7 days until spores are formed on the mycelium.
[0055] (3-2) Preparation of solid medium: use bran as raw material, adjust moisture content to 40%-50%, autoclave at 121°C for 20min,
[0056] The bran after cooling was used as a solid medium for Aspergillus awamori (Aspergillus awamori) 2-17.
[0057] (3-3) Preparation of solid microbial agent: Wash the spores and mycelia of Aspergillus awamori 2-17 on the PDA plate with sterile water and inoculate them on the solid medium as an inoculum, and inoculate them at 28°C Cultivate for 7 days to carry out sufficient fermentation and spore produc...
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