Preparation and application of a strain of Aspergillus tubingensis and its metabolites for disease prevention and growth promotion
A technology of Aspergillus tabin and microorganisms is applied in the field of preparation of Aspergillus tabin and its metabolites, and can solve the problems of decreased control effect, destruction of biodiversity, excessive chemical pesticide residues and the like
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Embodiment 1
[0081] Embodiment 1, isolation and identification of Aspergillus tubingensis QF05
[0082] 1.1 Strain isolation
[0083] The strain was isolated from soil samples in special habitats of Qinghai-Tibet Plateau, Qinghai Province, China. Bacterial strains were separated by the dilution plate method, and the specific operation method was as follows: Weigh 10 g of the soil sample and put it into 90 ml of sterile water to vibrate evenly to obtain 10 -1 Concentration of bacterial solution, use a 1ml sterile pipette to draw 1ml 10 -1 Concentration of bacterial solution in a tube of 9ml sterile water, shake well that is 10 -2 Concentration of bacterial solution, the same method, sequentially diluted to 10 -4 . the above 10 -2 、10 -3 and 10 -4 Spread the soil bacteria solution on the PDA plate respectively, dry it and place it upside down in a 25°C incubator for 3-5 days. After the isolated fungal single colony is purified, transfer it to a PDA slant for culture. After it grows we...
Embodiment 2
[0094] Embodiment 2, Aspergillus tubingensis (Aspergillus tubingensis) QF05 is to the competitive inhibitory effect of testing pathogenic bacteria
[0095] Pick the Aspergillus tubingensis (Aspergillus tubingensis) QF05 bacterium cake with a diameter of 7mm grown on the flat plate and the bacteria cake of the pathogenic bacteria for testing, and inoculate them symmetrically on the PDA medium respectively at a position 2cm from the center, and the control does not inoculate Aspergillus tubingensis (Aspergillus tubingensis) tubingensis) QF05 bacterium cake, only inoculate the test pathogen bacterium cake, each treatment was repeated three times, and cultured at 25°C for 4 days to observe the growth of the pathogen. The tested pathogens include: Botrytis cinerea, Fusarium moniliforme, Colletotrichum capsici, Fusarium oxysporum f.sp.cucumerinum, Rhizoctonia cereali), Alternaria tenuissima, Fusarium oxysporum f. sp. conglutinans, Monilinia fructicola.
[0096] The results showed t...
Embodiment 3
[0100] Embodiment 3, Aspergillus tubingensis (Aspergillus tubingensis) QF05 aseptic fermentation filtrate is to the inhibitory effect of testing pathogenic bacteria
[0101] 1. Preparation of Aspergillus tubingensis QF05 sterile fermentation filtrate
[0102] Pick up the Aspergillus tubingensis QF05 grown on the plate with the inoculation loop and inoculate it into a 500mL Erlenmeyer flask containing 100mL of liquid fermentation medium, culture it on a shaker at 150rpm at 25°C for 4 days, collect the fermentation broth, and use a 0.22μm micropore Filtering the fermentation liquid with a filter membrane to remove Aspergillus tubingensis QF05 cells in the culture to obtain Aspergillus tubingensis QF05 sterile fermentation filtrate.
[0103] Among them, the liquid fermentation medium is maltose 20g, glycerin 20ml, beef extract 30g, peptone 30g, distilled water to 1000mL, sterilized at 121°C for 20min to obtain the liquid fermentation medium.
[0104] 2. Antibacterial effect
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