Chaetomium globosum and application of chaetomium globosum in preparation of medicament for preventing and treating wheat sharp eyespot
A kind of technology of Chaetomium globulus, Chaetomium spores, applied in the field of microorganisms
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0020] The separation of embodiment 1 Chaetomium globosa strain
[0021] At the wheat grain filling stage, the uninfected plants in the wheat field were collected in Changge County, Henan Province, and put into paper bags. The samples were stored in a refrigerator at 4°C. Rinse the root of the sample, and then take 2-3cm of wheat root tissue, disinfect the surface with 75% absolute ethanol for 10-30s, sterilize with 1% NaClO for 1.5min, rinse with sterile water for 3 times, and blot dry with sterile filter paper After hydration, cut into small sections of about 0.5 cm, and place them on a potato dextrose agar medium (PDA, raw material composition: 300 g of peeled potatoes, 20 g of glucose, 20 g of agar and 1000 ml of distilled water) with sterile tweezers. After 5-7 days of under-cultivation, the edge mycelia were picked and grown on a new PDA plate. After 5-7 days under the same conditions, the mycelium pieces with uniform colonies were picked and cultured on a PDA slant, an...
Embodiment 2D
[0022] Example 2DNA Extraction
[0023] Pick the mycelium pieces onto the PDA medium, and after culturing at 20°C for 5-7 days, pick 5 edge mycelium pieces and place them evenly on a PDA plate covered with sterilized cellophane. After 3-5 days, scrape the mycelium with a sterilized small shovel, freeze it with liquid nitrogen, and store it in a refrigerator at -20°C. When extracting DNA, take out 20-25mg mycelium and put it into a pre-cooled 1.5ml EP tube; add a little liquid nitrogen and grind the mycelium to powder in the EP tube with a pre-cooled iron nail; add 500μL Extraction Buffer (50mM Tris- Cl (pH 8.0), 150mM NaCl, 100mM EDTA (8.0)), oscillated on a vortex shaker to suspend the precipitate and mix well; Mix upside down, place in a water bath at 37°C for 1-3h; then add 75 μL of 5M NaCl, mix upside down; add 65 μL of CTAB / NaCl (10% CTAB, 0.7M NaCl) solution, bathe in water at 65°C for 30 min; add etc. volume (700 μL) of Tris-phenol: chloroform: isoamyl alcohol (25:24:...
Embodiment 3
[0024] Example 3 identification
[0025] This test uses primers ITS1 (5'-TCC GTA GGT GAA CCT GCG G-3', as shown in SE ID NO.1) and ITS4 (5'-TCC TCC GCT TAT TGA TAT GC-3', as shown in SEQ ID NO. .2) to amplify the DNA fragments containing ITS1, 5.8S rDNA and ITS2 of the strain to be tested. The system refers to Daval et al. (2010). Amplification reaction conditions: PCR reaction program: 95°C for 3min; 95°C for 45s, 50°C for 30s, 72°C for 1min, 35 cycles; 72°C for 10min. After the PCR product was sequenced, the BLAST sequence alignment analysis was carried out in NCBI, and the sequence alignment result showed that the strain was Chaetomium globosa. The accession number of the ITS sequence on NCBI is OK287116, and the strain was deposited in the General Microbiology Center of the China Committee for the Collection of Microbial Cultures. The preservation date is August 4, 2020, and the preservation number is CGMCC No.19939. The preservation address is: No. 3, No. 1 Yard, Beich...
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