Aspergillus aculeatus strain and application thereof
A technology of Aspergillus aculeatus and Aspergillus aculeatus, which is applied in application, fungicides, fungi and other directions, can solve problems such as pesticide residues, and achieve the effect of promoting growth
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Embodiment 1
[0026] Example 1: Isolation, purification and identification of strains
[0027] 1. Soil collection: In this experiment, the soil for growing grapes in Ninghe, Tianjin, China was collected. The collected soil samples were stored at 4°C for use in screening soil fungi.
[0028] 2. Separation and purification of soil fungi: (1) Add 5g of soil to 1% saline to form soil dilutions of 1:102, 1:103, 1:104, 1:105, and 1:106, and shake them enough Draw 100 μL of each of the above-mentioned soil dilutions with different sparseness and apply them on the PDA solid medium containing ampicillin, and then place the PDA solid medium at 28°C for 2 to 3 days. (2) After culturing, select typical fungal colonies on the PDA solid medium and continue pure culture to obtain Aspergillus aculeatus Chinese Common Microorganism Collection Management Center (CGMCC) No. 17191.
[0029] 3. Strain identification: (1) Extract fungal DNA by CTAB method. The genomic DNA of strain TJ was extracted using the fungal g...
Embodiment 2
[0030] Example 2: Experiment to promote the growth of cucumber plants
[0031] 1. Fermentation of strains
[0032] Medium: PDB medium (200g potato, 20g glucose, 1000mL water, natural pH)
[0033] Strain culture: Put a little fungus in the solid PDA medium into the liquid medium formula (200g potato, 20g glucose, 16g agar powder, 1000ml distilled water, sterilized at 121°C for 20min), put it in the shaker box and shake it for cultivation time 7-10d.
[0034] 2. Cucumber seedling irrigation
[0035] Take 20mL and 10mL of the shaken bacteria and pour them into a 500mL Erlenmeyer flask respectively, add distilled water to 400mL and 500mL, and dilute it to a constant volume of 20 times and 50 times of the same bacterial liquid with different concentrations, Distilled water was used as a control. Pour the diluted liquid evenly into the soil around the roots of the plants in the seedling tray, and pour 10 mL of each seedling plant.
[0036] 3. Determination of Cucumber Growth Index
[0037] Me...
Embodiment 3
[0044] Example 3: Experiment of inducing cucumber resistance to Fusarium wilt
[0045] 1. Fermentation of strains
[0046] Medium: PDB medium (200g potato, 20g glucose, 1000mL water, natural pH)
[0047] Strain culture: Put a little fungus in the solid PDA medium into the liquid medium formula (200g potato, 20g glucose, 16g agar powder, 1000ml distilled water, sterilized at 121°C for 20min), put it in the shaker box and shake it for cultivation time 7-10d.
[0048] 2. Cucumber seedling irrigation
[0049] Take 20mL and 10mL of the shaken bacteria and pour them into 500mL Erlenmeyer flasks, add distilled water to 400mL and 500mL, and dilute them to 20 times and 50 times of the same bacteria with different concentrations. The diluted liquid and the volume mixture of cucumber Fusarium wilt solution 2:1, 3:1, the cucumber seedlings in each pot are irrigated with 5mL roots, and 5ml of cucumber fusarium wilt solution is set to irrigate the roots. Observe the phenomenon in the clear water (C...
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