Application of 1% isothiazolinone.2% methylene bisthiocyanate missible oil in prevention and treatment of bacterial fruit blotch, and 1% isothiazolinone.2% methylene bisthiocyanate missible oil
A technology of dithiocyanomethane and isothiazolinone, applied in application, biocide, disinfectant, etc., can solve problems such as infection and economic loss, and achieve the effects of promoting root growth, reducing pollution, and increasing germination rate
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Embodiment 1
[0030] 1. Indoor Toxicity Assay
[0031] Indoor toxicity was determined by the zone of inhibition method. A single colony of Pseudomonas spp. was inoculated in liquid KB medium, cultured at 28°C, 200rpm / min for 24h, OD 600 ≈0.3 (10 8 cfu / mL). When the temperature of the medium drops to about 50°C, add the bacterial solution into the medium (the ratio of the bacterial solution to the medium is 1:40) to make a plate. A 7mm diameter sterile filter paper disc was placed in the plate. Take 10uL of different concentrations of test agents and drop them into the filter paper. Sterile water was used as control, and each treatment was repeated 3 times. After culturing at constant temperature for 48 hours at 28°C, measure the diameter of the inhibition zone with a cross (see figure 1 ).
[0032] 2. Result Analysis
[0033] 2.1. Indoor virulence
[0034] The results of the toxicity test are shown in Table 1. It can be seen from Table 1 that among the 5 kinds of medicaments teste...
Embodiment 2
[0043] 1. Seed treatment
[0044] Adjust the Aac-5 bacterial solution to 10 8 cfu / mL, mixed at the ratio of 1g of melon seeds and 2mL of bacterial solution, soaked for 1h, and dried the seeds in an ultra-clean workbench. See Table 4 for the test agents, treatment concentrations and time. After the agent treatment, the seeds were rinsed with water for 3 times. The seeds were placed on the water agar plate, and the sterilized filter paper was soaked in water and covered the seeds. 50 seeds per dish, repeated 3 times. Accelerate the germination at 28°C, investigate the germination rate of the seeds after 16 hours, and measure the root length after 48 hours, so as to judge the effect of the chemical treatment on the germination of the seeds. The remaining seeds of the same treatment were sown in sterilized soil, and each treatment was repeated 3 times, with 15 seedlings per repetition. Clear water was used as a control. On the 5th day after emergence, the number of cotyledon ...
Embodiment 3
[0063] 1. Spray concentration detection
[0064] 72% agricultural streptomycin sulfate, 30% copper succinate and 1% isothiazolinone·2% dithiocyanomethane emulsifiable concentrate were used for the test agent, and 5 concentrations were set: 1200 times liquid, 1000 times liquid, 800 times liquid, 500 times liquid and 200 times liquid. Spray on melon seedlings and watermelon seedlings, repeat 4 times for each concentration, 15 seedlings for each repetition, control with clean water, and investigate the phytotoxicity after 7 days.
[0065] 2. Results and Analysis
[0066] 2.1 Analysis of test results
[0067] After spraying watermelon and melon seedlings with 72% agricultural streptomycin sulfate, copper succinate, and 1% isothiazolinone·2% dithiocyanomethane emulsifiable concentrate, the plants showed different drug resistance. Not the same. After spraying the leaves of watermelon and muskmelon with 3 kinds of agents at 1000 times of liquid, the plants all grew healthy and gr...
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