Aspergillus fumigatus strain and application thereof
A technology of Aspergillus fumigatus and strains, applied in the field of microorganisms, can solve the problems of not being easy to use effectively, occupying land resources, heavy metal pollution, etc., and achieve the effects of improving the ability to absorb phosphorus, increasing the phosphorus absorption coefficient, and relieving pressure
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Embodiment 1
[0034] Example 1: Isolation and screening of functional strains
[0035] 1) Collection of samples
[0036] (1) The samples were collected from coal gangue hills and nearby soil in a coal production area in Guizhou. Select the soil at the root of the plant that grows well, first shovel off the surface soil, dig 10-20cm along the root of the plant, and use the "root shaking method" to collect the soil in a sterile ziplock bag.
[0037] (2) The ice box is sealed and taken back to the laboratory. After removing the plant residues, crush them through a 20-mesh sieve.
[0038] (3) Store the samples in a refrigerator at 4°C for refrigerated storage.
[0039] 2) Screening of functional strains
[0040] (1) Accurately weigh 1 g of the sample into a sterilized 250 mL Erlenmeyer flask, and add 99 mL of sterile water.
[0041] (2) Shake for 30 minutes in a constant temperature shaker at 170r / min and around 28°C.
[0042] (3) After shaking for 30 minutes, take the supernatant and dilu...
Embodiment 2
[0049] Embodiment 2: the drawing of the growth curve of functional bacterial strain
[0050] 1) Preparation of fungal spore suspension: use an inoculation needle to pick the mycelia of the fungus to be tested on the PDA slant medium, activate at 30°C for 36-72 hours, take out after a large number of fungal spores grow, and use 5mL sterile distilled water on the ultra-clean workbench Rinse the slope, make a suspension of fungal spores, dilute to 100mL, shake well and set aside.
[0051] 2) Inoculation and cultivation: Pour 100mL LB liquid medium into a 250mL Erlenmeyer flask, prepare a total of 30 bottles, put them into an autoclave for sterilization at 121°C for 30min, and inoculate the prepared fungal spore suspension at 5% Add the amount into the sterilized LB liquid medium, 170r·min -1 , 30 ℃ shaker cultivation. Mark the bacteria number and culture time on the Erlenmeyer flask.
[0052] 3) Determination: Take out 3 bottles every 24 hours, dry the blank filter paper at 10...
Embodiment 3
[0054]Embodiment 3: the identification of functional bacterial strain
[0055] In the present invention, the fungus GZT-Asp01 entrusts China Center for Type Culture Collection to identify it.
[0056] 1) Colony appearance
[0057] The primary hyphae of the fungus GZT-Asp01 are white, hairy, protruding in the middle of the colony, and spread radially. After 5 days, smoke green spores began to appear in the middle of the colony. After about 9 days, the mycelium can cover the entire plate, and the culture can be seen from the back of the plate. The basal matrix turns yellowish brown, such as figure 2 shown.
[0058] 2) Microscopic morphology of fungi
[0059] The GZT-Asp01 fungus was stained with safranin, and the microscopic morphology of the fungus was observed under an optical microscope after staining. It can be observed with an optical microscope that the hyphae of the GZT-Asp01 fungus are transparent, and the top of the conidiophores swells into an apical capsule, whic...
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