A Strain of Pseudomonas stutzeri and Its Application
A technology of Pseudomonas stutzeri and Bacillus, applied in the direction of application, bacteria, and fungicides, can solve the problems of long cycle of disease-resistant varieties, single resistance, and pesticide residues, and achieve good application prospects, fast growth, and high yield. The effect of large amount of spores
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Embodiment 1
[0022] 1. Isolation and purification of Pseudomonas stutzeri strain YT2003
[0023] The Pseudomonas stutzeri strain YT2003 of the present invention is obtained from the soil by the dilution plate method and the plate streaking method. The separation method is as follows:
[0024] (1) Separation of bacilli: soil samples are collected, and plots of different types of crops are selected in different regions of the country, and the 5-point sampling method is adopted to collect appropriate amounts of soil around the plot and the central depth within the range of 10-20cm, etc. Mix well. Indicate the location, time and person of collection. Weigh 1g soil sample in 100mL sterile water, place it in a shaker at 30℃, shake at 150rpm for 10min, then incubate it in a water bath at 60℃ for 30min, take 100μL of 10-2, 10-3, 10-4 dilution for coating On the LB medium plate, each gradient was coated in three parallels. After culturing at 30°C for 2 days, the microbial colonies of different forms o...
Embodiment 2
[0036] Fermentation process of Pseudomonas stutzeri strain YT2003
[0037] LB liquid medium: The formula is: tryptone 10g, yeast extract 5g, sodium chloride 10g, distilled water 1000mL, pH adjusted to 7.0-7.2.
[0038] Mass fermentation medium formula (mass percentage): soy flour 3.0%, corn flour 3.0%, light calcium carbonate 0.2%, sodium chloride 0.1%, the rest is water, pH 7.3.
[0039] Mass fermentation process of Pseudomonas stutzeri strain YT2003:
[0040] ①Bacterial seed liquid culture: pick a small amount of bacteria from the slope of the test tube from the Pseudomonas stutzeri strain YT2003, transfer to LB liquid medium, shake culture at 30℃ for 3-5 days, this is the seed liquid;
[0041] ② Mass solid fermentation: Inoculate a large amount of fermentation medium with the seed liquid inoculation ratio of 1:90. Place the inoculated raw materials in a fermentation room (30°C and relative humidity above 85%) for fermentation and culture for 3-5 days. After drying, the original Pseu...
Embodiment 3
[0043] Field efficacy test
[0044] This example provides related experiments on the control effect of Pseudomonas stutzeri strain YT2003 on watermelon fusarium wilt.
[0045] 1) Test medicine
[0046] Pseudomonas stutzeri strain YT2003 original powder (prepared in Example 2); 70% thiophanate methyl wettable powder (commercially available).
[0047] 2) Test crops and control objects:
[0048] The test crop was watermelon; the variety was Qilin 8424;
[0049] Control object: Fusarium wilt.
[0050] 3) Test site conditions, test design and arrangement
[0051] The test site was set up in the watermelon field in Xinhu Village, Wanglao Township, Dongying City, Shandong Province. The soil was clay soil, and fusarium wilt was severe in previous years. The cultivation conditions of the experimental sites are uniform.
[0052] The ratio of Pseudomonas spp. YT2003 original powder in this test facility is 1:200, 1:400, 1:600; 70% thiophanate-methyl WP 1:600; clean water is used as a control for a to...
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