Aureobasidium aureum MR-57 and application thereof
A technology of MR-57 and spores, applied in the field of MR-57 and its application field, can solve the problem of limited strain resources
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Embodiment 1
[0038] Screening, Identification and Preservation of Example 1 Bacterial Strain MR-57
[0039] 1. Screening
[0040] (1) The soil to be tested is 1-year-old rhizosphere soil, air-dried and passed through a 20-mesh sieve; weigh 10g of the sample in a 250mL Erlenmeyer flask containing 90mL of sterile saline and glass beads; take 1mL of the supernatant after fully shaking for 20min solution, add 9mL sterile saline to obtain a 10-fold dilution, and serially dilute to 10 -3 、10 -4 、10 -5 Standby; draw 200 μL dilutions of different gradient solutions and spread them on the plate containing PDA medium, and each treatment has 3 replicates; culture in the dark at 25°C for 7 days to select single colonies with different phenotypes and pass them for 3 times, and streak on The PDA medium was purified and cultured, and pure colonies were isolated and stored at 4°C.
[0041] (2) The bacterial strains obtained in the previous step were screened by plate confrontation culture method, and ...
Embodiment 2
[0055] The broad-spectrum antibacterial test of embodiment 2 bacterial strain MR-57
[0056] Rhizoctonia solani, Phytophthora cactorum, Botrytis cinerea, Fusarium oxysporum, Fusarium equiseti, Alternaria tenuissima, Alternaria liriodendra 9 pathogenic bacteria, Cylindrocarpon destructans, Mycocentrospora acerina, and Mycocentrospora acerina were used as target bacteria, and the antimicrobial spectrum test was carried out on the strain MR-57 by plate confrontation method. details as follows:
[0057] By confronting the culture method in the petri dish, get the test pathogenic bacteria bacterium cake (Rhizoctonia solani, Phytophthora cactorum, Botrytis cinerea, Fusarium oxysporum, Fusarium oxysporum, Fusarium equiseti, Alternaria tenuissima, Alternaria liriodendra, Cylindrocarpondestructans, Mycocentrospora acerina) and inoculate to the center of a plate containing PDA medium with a diameter of 90mm, At the same time, two bacterium cakes of strain MR-57 with a diameter of 8 mm...
Embodiment 3
[0063] Example 3 Bacterial strain MR-57 fermented liquid inhibits the growth of Fusarium equisetum mycelia
[0064] (1) Activation of test pathogenic bacteria and preparation of bacterial strain MR-57 fermentation broth
[0065] After placing Fusarium equiseti at room temperature for 30 minutes, pick the mycelia of Fusarium equiseti under aseptic conditions and inoculate them in the center of the plate containing PDA medium, and culture them upside down at 25°C. The filaments were subcultured to the 4th generation for later use.
[0066] Pick a single colony of strain MR-57 and put it into a 250mL Erlenmeyer flask containing 100mL of PDB culture solution, culture it with shaking at 25°C and 170r / min for 7 days, then filter it through 3 layers of gauze, and filter the obtained filtrate through a 0.22μm filter membrane to obtain Strain MR-57 sterile fermentation broth.
[0067](2) The bacterial strain MR-57 sterile fermented liquid is mixed with the PDA medium according to the...
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