Preparation method of Isaria javanicus conidium microcapsules
A technology of Corynebacterium javanica and conidia, which is applied in the field of pest biological control and achieves the effects of important popularization and application value, low cost of raw materials and easy operation.
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Embodiment 1
[0043] Example 1 Preparation of 10% (pure pollen / composite glue W / W) conidia microcapsules of Corynespora javanica
[0044] figure 1 Be the preparation flowchart of Corynespora Javanese conidia microcapsules, specifically comprise the following steps:
[0045] S1. Preparation of cystic core: Take 1 g of pure sporopollen of Corynespora javanica SP053 strain, add 10 mL of 0.05% Tween 80 solution, vortex and stir, prepare bacterial suspension, and set aside.
[0046] S2. Preparation of capsule wall: take 5 g of gelatin, add 35 mL of distilled water to soak and swell, and heat to dissolve into a solution; take 5 g of gum arabic, add 35 mL of distilled water and heat to about 80°C to dissolve into a solution; keep both solutions at 40°C for later use .
[0047] S3. Preparation of microcapsules: under the condition of 40°C water bath, mix the gelatin solution and the capsule core material, and stir gently evenly. After 5 minutes, add gum arabic solution with the same qua...
Embodiment 2
[0048] Example 2 Preparation of 5% (pure pollen / composite glue W / W) conidia microcapsules of Corynespora javanica
[0049] figure 1 Be the preparation flowchart of Corynespora Javanese conidia microcapsules, specifically comprise the following steps:
[0050] S1. Preparation of cystic core: Take 0.5 g of pure sporopollen of Corynespora javanica SP053 strain, add 5 mL of 0.05% Tween 80 solution, vortex and stir, prepare bacterial suspension, and set aside.
[0051] S2. Preparation of capsule wall: take 5 g of gelatin, add 35 mL of distilled water to soak and swell, and heat to dissolve into a solution; take 5 g of gum arabic, add 35 mL of distilled water and heat to about 80°C to dissolve into a solution; keep both solutions at 40°C for later use.
[0052] S3. Preparation of microcapsules: under the condition of 40°C water bath, mix the gelatin solution and the capsule core material, and stir gently evenly. After 5 minutes, add gum arabic solution equivalent to the g...
Embodiment 3
[0062] Example 3 Performance determination of conidia microcapsules
[0063] After sample preparation of the microcapsule dry powder prepared in Example 1 and Example 2, scanning electron microscope observation was carried out, and the results showed that the microcapsules were all spherical in shape, uniform in size, smooth in surface, and had little difference in diameter, with an average particle size of 20- 30 μm ( image 3 ).
[0064] Detection of conidia germination rate: Take 5-10 mg of conidia microcapsules prepared in Example 1 and Example 2, add 100 mL of 0.05% Tween 80 aqueous solution, vibrate to break the wall, and filter through three layers of gauze to obtain The conidia suspension was cultured at 25°C for a certain period of time, and the germination rate was checked. The result is as Figure 4 As shown, after the conidia microcapsules were stored for 180 days, the germination rate of conidia remained above 90%, while the germination rate of conventional c...
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