Strain of pseudomonas stutzeri and application thereof
A technology of Pseudomonas stutzeri and Gram-positive bacteria, applied in the field of Pseudomonas stutzeri, can solve the problems of long cycle of disease-resistant varieties, single resistance, pesticide residues, etc., and achieve good application prospects, growth The effect of fast speed and strong resistance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0022] 1. Isolation and purification of Pseudomonas stutzeri strain YT2003
[0023] Pseudomonas stutzeri bacterial strain YT2003 of the present invention adopts dilution plate method and plate streaking method to separate and obtain from soil, and separation method is:
[0024] (1) Separation of bacilli: the collection of soil samples, select plots planted with different types of crops in different regions of the country, and adopt the 5-point sampling method to collect the appropriate amount of soil around and in the center of the plot within a depth of 10-20 cm. Mix in equal amounts. Indicate the location, time and person of the collection. Weigh 1g of soil sample into 100mL sterile water, place it in a shaker at 30°C at 150rpm for 10min, then place it in a water bath at 60°C for 30min, take 100μL of 10-2, 10-3, 10-4 dilution to coat On the LB medium plate, each gradient was coated in three parallels, and after culturing at 30°C for 2 days, microbial colonies of different ...
Embodiment 2
[0036] Fermentation process of Pseudomonas stutzeri strain YT2003
[0037] LB liquid medium: formula: tryptone 10g, yeast extract 5g, sodium chloride 10g, distilled water 1000mL, pH adjusted to 7.0-7.2.
[0038] A large amount of fermentation medium formula (mass percentage content): 3.0% of soybean flour, 3.0% of corn flour, 0.2% of light calcium carbonate, 0.1% of sodium chloride, the rest is water, pH 7.3.
[0039] Mass fermentation process of Pseudomonas stutzeri strain YT2003:
[0040] ① Strain seed liquid culture: Pick a small amount of bacteria of Pseudomonas stutzeri strain YT2003 from the slant of the test tube, transfer it to LB liquid medium, shake and culture at 30°C for 3-5 days, and this is the seed liquid;
[0041] ②Massive solid fermentation: inoculate the seed solution in a large-scale fermentation medium at a ratio of 1:90. The inoculated raw materials are placed in a fermentation room (at 30° C. and a relative humidity above 85%) for fermentation and culti...
Embodiment 3
[0043] field efficacy test
[0044] This example provides related experiments on the control effect of the original powder of Pseudomonas stutzeri strain YT2003 on watermelon wilt.
[0045] 1) Test drug
[0046] Pseudomonas stutzeri strain YT2003 raw powder (prepared in Example 2); 70% thiophanate-methyl wettable powder (commercially available).
[0047] 2) Test crops and control objects:
[0048] The test crop is watermelon; the variety is Qilin 8424;
[0049] Control object: Fusarium wilt.
[0050] 3) Test site conditions, test design and arrangement
[0051] The test site is located in the watermelon field of Xinhu Village, Wanglao Township, Dongying City, Shandong Province. The soil is clay soil, and the occurrence of Fusarium wilt was heavy in previous years. The cultivation conditions in the experimental field were uniform.
[0052] In this test facility, the ratio of the original powder of Pseudomonas spp. YT2003 was 1:200, 1:400, 1:600; 70% thiophanate-methyl wet...
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