Penicillium sp. strain and application thereof
A technology of Penicillium and strains, applied in the application, fungicides, fungi and other directions, can solve the problems of unformed products such as anthracnose.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0064] Strain acquisition:
[0065] The bacterial strain of the present invention is obtained by separation, purification and culture according to the conventional method of air microorganism separation, and the medium used for separation is tiger red medium, which is identified as Penicillium sp. by fungal ITS and named YAnti45-1. figure 1 The blast gene comparison results of YAnti45-1 Penicillium strain on Genbank, figure 2 It is the NJ phylogenetic tree of the YAnti45-1 Penicillium strain. It can be seen from the figure that the YAnti45-1 strain belongs to the Penicillium genus, and there are obvious differences between the YAnti45-1 Penicillium strain and other strains.
[0066] Morphology: On the CMD medium, the conidia area presents protrusions of different sizes, and the aerial hyphae are not luxuriant. On the PDA medium, the aerial mycelium is luxuriant, and the sporulation area spreads all over the entire plate, dark green to gray green, and produces yellow pigment ...
Embodiment 2
[0072] 1. Cultivate the YAnti45-1 strain on a PDA plate, and take it out for later use when spores grow on the plate;
[0073] 2. Collect the spores on the plate under sterile conditions, insert the spores into the PDA liquid medium containing glass beads, and culture at 27°C 120rpm / min;
[0074] 3. Cultivate for 2 days, and wait until the medium is covered with tiny mycelium balls, this is the Penicillium seed solution;
[0075] 4. Aseptically insert the grown penicillium seed liquid into the pre-sterilized liquid fermentation medium (10 grams of cold-pressed bean cake powder, 10 grams of fructose), and the amount of insertion is 1% of the liquid fermentation medium loading % calculation, cultured at 26°C for 4 days, dissolved oxygen was 71% (rotating speed was 158rpm / min) in 0 to 36 hours, and cultivated after 36 hours at 60% dissolved oxygen (rotating speed was 133rpm / min);
[0076] 5. The antagonism ability of the YAnti45-1 strain culture to anthrax bacteria was measured by...
Embodiment 3
[0078] 1. Cultivate the YAnti45-1 strain on a PDA plate, and take it out for later use when spores grow on the plate;
[0079] 2. Collect the spores on the plate under sterile conditions, insert the spores into the PDA liquid culture containing glass beads, and cultivate at 30°C and 130rpm / min;
[0080] 3. Cultivate for 2 days, and wait until the medium is covered with tiny mycelium balls, this is the Penicillium seed solution;
[0081] 4. Aseptically insert the long-growing penicillium seed liquid into the pre-sterilized liquid fermentation medium (wherein 20 grams of cold-pressed bean cake powder, 20 grams of fructose), the amount of insertion is 2% of the liquid volume of the new medium % calculation, cultured at 28°C for 6 days, 0 to 36 hours dissolved oxygen was 75% (rotating speed was 168rpm / min), and after 36 hours dissolved oxygen was 70% (rotating speed was 156rpm / min) for cultivation;
[0082] 5. The antagonism ability of YAnti45-1 strain culture to anthrax bacteria...
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