Ustilago-maydis haploid strain UM02 and application thereof
A maize black powder fungus, UM02 technology, applied in the determination/inspection of fungi and microorganisms, microorganisms and other directions, can solve the problem of poor test accuracy, consistency and repeatability, uncertain results of artificial inoculation, and rot of corn plants. and other problems, to achieve the effect of strong pathogenicity, easy harvesting and transportation, and high success rate of inoculation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0038] Example 1 Isolation, screening and identification of haploid strains of Ustilago zeae of the present invention
[0039] Proceed as follows:
[0040] (1) Collect the teliospores and prepare the teliospore suspension: Naturally air-dried smut spore galls were collected in Hainan in December 2016, and a small amount of teliospores were directly picked from the smut spore galls and placed in a sterile In a 2ml centrifuge tube, add 1ml of 1% by weight sodium hypochlorite solution, mix by inversion for 2min, centrifuge at 12000rpm for 1min, remove the supernatant, add sterile water to wash the precipitate 3 times, and finally dilute the precipitate with sterile water. The teliospore suspension is obtained with a final concentration of 10 3 Spores / ml.
[0041] (2) Winter spore culture: Take 200 μl of the teliospore suspension obtained in step (1) and spread it on the PDA medium and culture it at 25° C. for 2 days, and then small colonies visible to the naked eye can be observed.
[0...
Embodiment 2
[0051] Example 2 Classification and identification of haploid strain UM02 of the present invention
[0052] (1) The morphological characteristics of the strain: The spores of this strain are short rod-shaped, without septa, and 15-25 μm in length.
[0053] (2) The culture characteristics of the strain: On the PDA plate medium, the colony is milky white, with wrinkles on the surface, and moist, similar to yeast colonies, but when picked, it is more viscous than bacterial and yeast colonies.
[0054] (3) Molecular identification of the haploid strain UM02 of the present invention:
[0055] Using the genomic DNA of the UM02 strain as a template, the fungal genome ITS segment was amplified by PCR using the fungal universal primers ITS1 and ITS4. The primer sequence is:
[0056] ITS1: 5’-TCCGTAGGTGAACCTGCGG-3’;
[0057] ITS4: 5’-TCCTCCGCTTATTGATATGC-3’.
[0058] The PCR reaction system (25μL), in which: ITS1 (10μmol / L) 0.5μL, ITS4 (10μmol / L) 0.5μL, Es Taq MasterMix (Kangwei Century) 12.5μL, te...
Embodiment 3
[0060] Example 3 Preparation of mother liquor for inoculation of haploid strain UM02 of the present invention
[0061] Proceed as follows:
[0062] (1) Strain activation: inoculate the low-temperature preserved UM02 strain on a PDA plate medium (the preparation method is: 200g potatoes are peeled and cut into small pieces, boiled in 800ml distilled water for 20 minutes, and filtered with 4 layers of gauze. Add 20g glucose and 20g agar, boil and dilute to 1000ml, sterilize at 121°C for 20min), culture at 25°C in the dark for 1 day to obtain activated strains.
[0063] (2) Bacterial cell preparation: Use an inoculating needle to pick an appropriate amount of the UM02 activated strain obtained in step (1) and evenly spread it on a PDA plate medium, culture at 25° C. and dark conditions for 3 days to obtain UM02 cell.
[0064] (3) Preparation of inoculation mother solution: Use sterile glass slides to scrape all the bacteria obtained in step (2) from the PDA plate medium and use 1L of the...
PUM
Property | Measurement | Unit |
---|---|---|
length | aaaaa | aaaaa |
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