Application of Bacillus aryabhattai in preparation of acid soil conditioner
A technology of Bacillus aeruginosa, acid soil, applied in the field of microorganisms
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Embodiment 1
[0042] The acid-base tolerance of Bacillus Ascheri with the deposit number CCTCC AB 207736:
[0043] Alkali resistance test:
[0044] Inoculate the Bacillus abbeyii seed solution into LB medium with different initial pH according to the inoculation amount of 5%, culture at 30℃ and 200r / min, and take samples at regular intervals to measure OD 600 , The measurement is not ended until the late stabilization period. The initial pH gradient of the medium is set to 7, 8, 9, 10.
[0045] LB medium: 10g peptone, 5g yeast extract, 10g NaCl, 1000mL distilled water, pH7.0, autoclaved at 121°C for 20min.
[0046] Test results such as figure 1 with figure 2 The pH in the two groups of pH9 and pH10 has been in a downward trend from the beginning to 23h. It may be that Bacillus Ascheri produces some acidic substance to neutralize the alkali in the culture medium in order to make the environment suitable for spontaneous growth.
[0047] In the pH7 and pH8 groups, the pH kept rising, indicating that t...
Embodiment 2
[0054] Phosphorus-dissolving ability of Bacillus Ascheri with the deposit number CCTCC AB 207736:
[0055] The seed solution was inoculated into a liquid phosphorus-dissolving medium according to the inoculum amount of 5%, cultivated at 30℃, 200r / min, and then the available phosphorus (soluble phosphorus) content in the culture solution was determined by the molybdenum blue colorimetric method to determine the solubility The strength of phosphorus.
[0056] Phosphate dissolution medium (PKO medium): glucose 10.0g, (NH 4 ) 2 SO 4 0.5g, NaCl 0.3g, KCl 0.3g, MgSO 4 ·7H 2 O 0.3g, FeSO 4 ·7H 2 O 0.03g, MnSO 4 ·7H 2 O 0.3g, poorly soluble phosphorus source, 1000mL of water, pH 7.0, high pressure steam sterilization at 115°C for 30 minutes; poorly soluble phosphorus source and dosage: tricalcium phosphate 0.5%, phosphate rock powder 0.5%, egg yolk lecithin 0.2% (phosphoric acid 0.5% of tricalcium means that 0.5 g of tricalcium phosphate is added to 100 mL of medium, and the rest are the ...
Embodiment 3
[0063] The inhibitory effect of Bacillus asheri with the deposit number CCTCC AB 207736 on plant pathogens:
[0064] The inhibition zone method was used to determine the inhibitory ability of Bacillus asheri on pathogens. Dilute the activated Bacillus argentii seed solution appropriately and spread it on a PDA plate, and spread sterile water as a control test group. Punch holes on the PDA plate covered with pathogenic fungi, pick the bacterial clumps and inoculate them upside down on the PDA plate coated with Bacillus Ascheri, contact the plate with fungi, and place the plate at 30°C for 7 days. Subsequently, the diameter of the fungal colony was measured and the inhibition rate was calculated to analyze the antibacterial effect.
[0065] The plant pathogens selected in this experiment include banana fusarium wilt pathogen, potato scab pathogen, verticillium fusarium, Fusarium oxysporum (2 strains), Fusarium solani (2 strains), Fusarium, Cladosporium, Ash Botrytis, Myrothecium sp...
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