Pseudomonas aeruginosa and application thereof
A technology of Pseudomonas aeruginosa and pathogenic bacteria, applied in the field of agricultural microorganisms, to achieve the effect of reducing the disease index and obvious control effect
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Embodiment 1
[0033] The isolation and screening of embodiment 1 Pseudomonas aeruginosa HZ15
[0034] 1. Separation and screening
[0035] The larvae of a certain Lepidoptera insect were collected by the Plant Protection College of Yunnan Agricultural University in the "Yunnan Provincial Coffee Coffea Seedling Breeding Base" in Nanping Town, Simao District, Pu'er City, Yunnan Province. Adopt the following method steps to obtain bacterial strain:
[0036] 1. Rinse the body surface of the larvae with 75% alcohol for 3 times, each time for 2 minutes, and then rinse with sterile water for 3 times, then dissect to obtain a complete digestive tract of the larvae.
[0037] 2. Sterilization: All experimental equipment such as petri dishes, centrifuge tubes, test tubes, and pipette tips and sterile water are sterilized by high pressure at 0.1MPa, 121°C, and sterilized for 30 minutes.
[0038] 3. Grinding: Cut the digestive tract of the obtained larva into pieces, put it into a sterile centrifuge t...
Embodiment 2
[0056] The screening of the fermentation culture condition of embodiment 2 Pseudomonas aeruginosa
[0057] Inoculate the Pseudomonas aeruginosa HZ15 bacterial liquid on the YSP medium, and cultivate it under the conditions of temperature 36°C, pH value 7, rotation speed 220r / min, liquid volume 40mL, inoculum volume 2.5%, time 48h, light 12h , to obtain Pseudomonas aeruginosa HZ15 fermentation broth, for the optimization of the following fermentation conditions.
[0058] 1. Optimal culture medium
[0059] The strains were cultured in five mediums: YSP, NYBD, NA, LB and CM.
[0060] Peptone yeast sucrose medium (YSP), including the following components: peptone 1.00g, yeast extract powder 0.50g, sucrose 2.00g, distilled water 100mL;
[0061] Beef extract yeast glucose medium (NYBD), including the following components: beef extract 0.80g, yeast extract powder 0.50g, glucose 1.00g, distilled water 100mL;
[0062] Nutrient agar medium (NA), including the following components: be...
Embodiment 3
[0095] The inhibitory effect of embodiment 3 Pseudomonas aeruginosa HZ15 fermented liquid to Phytophthora tabacum pathogenic bacteria
[0096] Using the plate confrontation method, use a sterile puncher (5mm) to punch holes on the pathogen plate, insert the bacteria block into the center of the newly prepared OA plate, and then use a sterile inoculation loop to pick the antagonistic bacteria separately from the center of the OA plate Inoculate antagonistic bacteria 4 times at equal distances around 2.5 cm, set 3 replicates, measure the colony diameter on the treated plate after culturing at 28°C for 5 days, take the average value to calculate the bacteriostatic rate, and determine its inhibitory effect. The control group was not inoculated with antagonistic bacteria.
[0097]
[0098] like Figure 12 The results shown show that the colony diameter on the treated plate is about 2.01 cm, and the inhibition rate of Pseudomonas aeruginosa HZ15 on Phytophthora nicotianae is abo...
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