Burkholderiaspp.and application thereof in preventing and treating main pathogenic bacteria of panax notoginseng root rot
A Burkholderia and Panax notoginseng technology, applied to Burkholderia strains and its application in the prevention and treatment of the main pathogenic bacteria of Panax notoginseng root rot, can solve the problems of different genotypes, unsatisfactory effects, allergic reactions, etc., and achieve Enhance colonization, promote the formation of biofilm, and promote the effect of strain growth
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Embodiment 1
[0016] The isolation of embodiment 1 Burkholderia (Burkholderia) B36
[0017] A kind of Burkholderia (Burkholderiaspp.) B36 was isolated from the healthy rhizosphere soil of Panax notoginseng by plate separation method, and its morphology was identified. Shaped, yellow colonies, smooth and raised surface, irregular edges.
[0018] The preservation information of the Burkholderia spp. B36 is as follows: the preservation number is CGMCCNo.21179; the preservation unit is the General Microbiology Center of the China Committee for the Collection of Microorganisms; the preservation address is No. 1, Beichen West Road, Chaoyang District, Beijing 3 No., zip code: 100101; date of deposit is November 16, 2020.
Embodiment 2
[0019] Example 2 Burkholderia (Burkholderia) B36 to the main pathogenic bacteria rust rot and eggplant rot of Panax notoginseng root rot Inhibition of Fusarium
[0020] Fusarium solani and Cylindrocarpondestructans tested in this example were provided by the Plant Pathology Laboratory of Plant Protection College of Yunnan Agricultural University.
[0021] The specific method is as follows:
[0022] The inhibitory activity of Burkholderia B36 on the mycelial growth of the tested root rot fungus was determined by plate confrontation culture method. On the ultra-clean workbench, the Fusarium solani rot and the rust rot fungus grown on the PDA medium are used to make a bacterium cake with a 5mm puncher, and then the bacterium cake is transferred to the center of the PDA medium plate, Then use a sterile toothpick to inoculate the isolated and purified Burkholderia 2.5cm away from the pathogenic bacteria, set up 4 repetitions, take the plate with only pathogenic bacteria cakes ...
Embodiment 3
[0029] Example 3 Detection of Burkholderia B36 Degradability of Saponin Autotoxic Substances
[0030] Specific steps are as follows:
[0031] (1) Use an inoculation loop to pick a single purified Burkholderia B36 strain, inoculate it into 50 mL of NA liquid medium, place it on a shaker at 28°C and 150 r / min for overnight culture; then, take 100 μL of the bacterial liquid and add Into 200mL liquid medium with crude saponins of notoginseng as the sole carbon source (crude notoginseng saponins 1g / L), the treatment without adding bacterial solution was used as a blank control, and placed on a shaker for shaking culture (28°C, 150r / min ), each treatment was repeated three times, and samples were taken for measurement at 48h, 96h and 144h of culture.
[0032] Among them, the formula of NA medium is glucose 10g, peptone 5g, beef extract 3g, yeast extract 1g, agar powder 17g, water 1000mL.
[0033] (2) Take 100mL liquid (including the blank control) from each bottle of shaking cul...
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