A strain of albicans and its application
A technology of white sac rake tooth fungus and mycelium, applied in the direction of application, fungi, chemicals for biological control, etc., to achieve the effect of promoting root growth of crops, increasing yield, and promoting flowering
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Embodiment 1
[0026] Example 1: Isolation and identification of bacterial strains
[0027] 1. Isolation and screening of strains:
[0028] (1) Isolation of strains
[0029] Take fresh Daxinganling wild blueberry root samples and rinse them with running water, dry them with filter paper, cut them into appropriate sizes, wash them with sterile water for 3 times, and put them in 10% H 2 o 2 Sterilize in medium for 10 minutes, rinse 3 times with sterile water, soak in 6% sodium hypochlorite solution for 2 minutes, then rinse 3 to 5 times with sterile water, put it on a sterile filter paper, and blot the surface moisture. Use sterile scissors to cut into root segments of about 1 cm, and inoculate them on the PDA medium after high-temperature and high-pressure sterilization at 121° C. for 30 minutes. After being placed in an incubator at 23°C for 3-10 days, hyphae can be seen growing from the cut edge of the sample, which is repeatedly separated and purified on the plate until each plate conta...
Embodiment 2
[0044] Embodiment 2: the preparation of plant inducer
[0045] The specific preparation method is as follows:
[0046] 1. Fermentation culture:
[0047]The bacterial classification of Irpex lacteus PR2 isolated and preserved in Example 1 preserved on the slant of the test tube at 4°C was placed on the PDA medium, cultivated at 25°C for one week, and the agar was dug into pieces and inoculated in 50mL PDA medium. The 250mL Erlenmeyer flask of culture medium was cultivated at 25°C for 3 days on a rotary shaker at 180r / min as seeds, and inoculated into a 500mL Erlenmeyer flask containing 150mL fermentation medium with 10% of the amount, cultivated for 5 days under the same conditions, and terminated Ferment to obtain seed liquid.
[0048] PDA medium formula: potato 200g, glucose 20g, agar 20g, water 1000ml.
[0049] Fermentation medium formula: 1.0L of potato extract, 1.0g of yeast extract, 3.0g of peptone, 15.0g of glucose, and 17.0g of agar.
[0050] Preparation of potato e...
Embodiment 3
[0053] Embodiment 3: the application of plant inducer in potato growth promotion and production increase
[0054] 1. Test method:
[0055] The potato sowing date is April 18-19, 2015, the sowing density is 3300-3500 plants / mu, the ridge spacing is 55cm, and the plant spacing is 35cm. During the implementation process, the farming operations during the potato growing season are the same as field planting.
[0056] Treatment 1: conventional treatment, that is, when sowing, no endophyte extract (that is, the plant inducer prepared in Example 2) was added to spray the ditch; during the expansion period, amino acid water-soluble fertilizer was drip-irrigated with water.
[0057] Treatment 2: when sowing, endophyte extract (i.e. the plant inducer prepared in Example 2) 10ml / mu spray ditch; in the expansion stage, amino acid water-soluble fertilizer, drip irrigation with water.
[0058] Process 3: when sowing, endophyte extract (i.e. the plant inducer prepared in Example 2) 10ml / mu...
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