Photosynthetic bacterium capsulated rhodobacter strain, microbial agent, preparation method and application thereof
A technology of rhodobacter capsularis and photosynthetic bacteria, which is applied in the field of bacterial agents and its preparation, and strains of rhodobacter capsularis of photosynthetic bacteria, which can solve the problems of difficulty and high cost in the control of rice bacterial blight, and achieve drug resistance , low cost, and simple cultivation process
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[0035] According to another aspect of the present invention, there is also provided a method for preparing a biocontrol agent of the above-mentioned photosynthetic bacteria Rhodobacter capsular strain, comprising the following steps: S1, activation: the preserved species of photosynthetic bacteria Rhodobacter capsular strain Cultivate according to the double-layer plate culture method until the red single colony appears; S2, seed culture: insert the red single colony cultivated in step S1 into a serum bottle, and carry out seed culture to logarithm with photosynthetic bacteria liquid medium Obtain the bacterial liquid in the growth phase; S3, production culture: inoculate the bacterial liquid in the step S2 with an inoculum amount of 3% to 6% of the total volume of the photosynthetic bacteria strain production medium, and cultivate to the logarithmic growth phase to obtain the photosynthetic bacteria capsulated rhodobacter strain of biocontrol agents.
[0036] In this embodime...
Embodiment 1
[0052]Use the inhibition zone method to measure the inhibition of photosynthetic bacteria strain Rhodobacter capsulata A12 to the pathogenic bacteria that cause rice bacterial blight. Get 0.1ml of pathogenic bacteria and spread it on the LB flat plate, put a sterilizing steel ring in the center, and place it on the steel plate. Add 0.05ml of photosynthetic bacteria liquid to the circle, incubate at 30°C for 7 days, and observe whether there is a zone of inhibition.
Embodiment 2
[0054] Under greenhouse conditions, the 5×10 6 cfu / mL biocontrol agent of photosynthetic bacteria Rhodobacter capsularis A12 strain. Soak the rice seeds germinated to white at 30°C for 1 hour, sow the treated rice seeds in pots, and keep the seedlings at 28°C during the identification period. Cultivate in a greenhouse under 10h / d light conditions, and record the plant height regularly. Three representative plants were selected to measure the plant height and wet weight respectively. After the rice enters the seedling stage, the rice seedlings are inoculated with Xanthomonas oryzae, and the disease index is investigated 7 days after the inoculation and the control effect is calculated.
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