Bacillus mycoides and application thereof for promoting growth of liquidambar formosana
A technology of Bacillus mycoides and sweetgum, applied to Bacillus mycoides and its application field in promoting and promoting the growth of Chinese sweetgum, can solve the problem of no reports of Chinese sweetgum organophosphate-resolving bacteria, and types of organophosphate-resolving bacteria. And the number of different problems, to achieve the effect of excellent strain resources, promote growth and development, good degradation effect
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Embodiment 1
[0021] Example 1: Determination of Phosphorus Solubilization Capacity of FXY-WH10 Plate.
[0022] Egg yolk medium: beef extract 3.0g, peptone 10.0g, sodium chloride 5.0g, distilled water 1000mL, agar 15.0~18.0g, pH 7.0, sterilized, when the temperature drops to about 50℃, add 3~4mL to every 50mL Fresh egg yolk liquid (mix the egg yolk and sterile saline in equal volume), mix well, and pour the plate.
[0023] The FXY-WH10 strain that was activated twice was spot-attached to the yolk plate with a sterilized toothpick, and after incubating at 30°C for 3 days, the diameter of the phosphate zone and the colony diameter was measured, and the ratio of the phosphate zone to the colony diameter was calculated ( figure 1 ).
[0024] From figure 1 It can be seen that after the FXY-WH10 strain is cultured on a yolk plate, it can produce an obvious opaque phosphate ring. After measurement and calculation, the diameter of the phosphate ring is 30.15mm, the diameter of the colony is 14.08mm, and ...
Embodiment 2
[0025] Example 2: Determination of FXY-WH10 Liquid Phosphorus Solubilization Ability.
[0026] Monkina medium: glucose 10.0g, ammonium sulfate 0.5g, sodium chloride 0.3g, potassium chloride 0.3g, magnesium sulfate heptahydrate 0.3g, ferrous sulfate heptahydrate 0.03g, manganese sulfate tetrahydrate 0.03g, eggs Phospholipid 0.4g, calcium carbonate 5.0g, distilled water 1000mL, pH 7.0
[0027] Inoculate the activated FXY-WH10 strain twice into NA medium (beef extract 3.0g, peptone 10.0g, sodium chloride 5.0g, distilled water 1000mL, agar 18.0g, pH 7.2~7.4). After incubating at 30°C for 2 days, nothing Rinse the cells with bacteria water to make a bacterial suspension. Take 1 mL of the bacterial suspension in a 100 mL Erlenmeyer flask containing 50 mL of Monkina medium, and use the Monkina medium containing 1 mL of sterile bacterial suspension as a control (CK). Three replicates of each treatment, 30°C, 200r / min shaking culture for 72h, the fermentation broth was centrifuged at 4°C, ...
Embodiment 3
[0029] Example 3: FXY-WH10 greenhouse pot experiment.
[0030] After activating FXY-WH10 for 2~3 times, use an inoculating loop to pick a small amount of bacteria and inoculate it in a 100mL Erlenmeyer flask containing 50mL NB medium (3g beef extract, 10g peptone, 5g sodium chloride, 1000mL distilled water, pH 7.2~7.4) , 30℃, 200r / min shaking culture for 48h. The fermentation broth (4℃, 6000r / min) was centrifuged for 5 minutes, and the bacteria were rinsed with sterile saline for 3 times, and then the bacteria suspension (10 8 cfu / mL) made into bacteria. Chinese Liquidambar formosana (seedling age 60 days) was inoculated, and the same amount of sterile saline was used as the control, and the inoculation amount was 5 mL / plant. 8 replicates for each treatment, placed in a greenhouse for unified management, light is 12h / day, and watered in time.
[0031] The effect of FXY-WH10 strain inoculation for 90 days on the growth of annual Chinese Liquidambar seedlings (see Table 1). From T...
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