Application of Bacillus velezensis YM-11-C for preventing and curing colletotrichum gloeosporioides Penz.
A technology for bacillus and anthracnose, applied in the application, bacteria, fungicides and other directions, can solve the problems of high cost and drug resistance of pathogenic bacteria, and achieve the effect of good effect, reduction of secondary pollution, good effect and prospect
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Embodiment 1
[0038] The isolation, screening and identification of embodiment 1 Veles bacillus YM-11-C
[0039] 1.1 Isolation of bacteria
[0040] Take a healthy mango epidermis, and in an ultra-clean workbench, first sterilize it with 75% alcohol for 10 seconds, then sterilize it with 2% NaClO for 1 minute, and finally rinse it with sterile water for 3 times, cut it into tissue pieces of about 3×3mm, After drying. Place 3-4 tissue pieces on the PDA medium and culture them in a 25°C incubator for 3-5 days. When colonies grow out of the tissue blocks, bacteria with different colony forms are picked to be purified and cultured on PDA medium and labeled.
[0041] 1.2 Primary screening of bacteria
[0042] Preliminary screening: Using the plate confrontation method, use a strain of Mango anthracis as an indicator bacterium to screen the bacterial strains isolated and purified in 1.1 on a PDA plate, and save the antagonistic strains for future use.
[0043] Re-screening: Screen the bacteria...
Embodiment 2
[0049] The influence of embodiment 2 Veles bacillus YM-11-C fermented liquid on mango anthracnose mycelium
[0050] The mango anthracnose fungus Colletotrichum fructicola was activated on a PDA plate and cultured at a constant temperature of 25°C for 5-7d. Use a sterilized puncher with a diameter of 5 mm to punch holes in the cultured anthrax bacteria, and place them in the center of a new PDA plate. With the center of the petri dish as the origin, place sterilized 5mm circular filter paper pieces at a distance of 2.5cm from the center, pipette 10 μL of bacterial solution with a pipette gun, and drop it on the filter paper pieces. Three replicates were set up for each treatment, and the treatment with water added was used as a control, and the culture was incubated at a constant temperature of 27°C. When the control colony is full of the plate, the diameter of the pathogenic bacteria colony is measured by the cross method, and the average value and the bacteriostatic rate are...
Embodiment 3
[0051] Embodiment 3 The impact of the volatile gas of Bacillus Velez YM-11-C on the hyphae of the mango anthracis fungus
[0052] Using the buckle method, put a sterile filter paper sheet with a diameter of 5mm in the center of the NA plate, and add 50μL of YM-11-C fermentation broth dropwise; use a puncher with a diameter of 5mm to cultivate the mango anthracnose bacteria for 5-7 days (Colletotrichum fructicola) bacterium cake was taken from the edge of the colony, and the bacterium cake was inoculated in the center of the PDA plate. The PDA plate inoculated with the mango anthracnose bacteria is buckled with the NA plate inoculated with the bacterial fermentation broth, and sealed. The NA plate not inoculated with bacterial fermentation broth was used as the control, and three replicates were set up for each treatment, and cultured at a constant temperature of 27°C. When the control colony is full of the plate, the diameter of the pathogenic bacteria colony is measured by t...
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