A strong phosphorus-soluble Bacillus subtilis and its carbon-based microbial compound fertilizer and its application
A technology of Bacillus subtilis and compound fertilizer, which is applied in strong phosphorus-soluble Bacillus subtilis and its carbon-based microbial compound fertilizer and its application field, can solve the problems of not being able to fully realize the value of fallen leaves, and achieve stable spore-producing ability and stable spore-producing Strong ability, effect of reducing nitrate content
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Embodiment 1
[0029] Example 1 Isolation and Identification of Bacillus subtilis CNBG-PGPR-1
[0030] (1) Sample dilution and coating
[0031] Take 0.5g soil sample (collected from the farmland around Nanjing, Jiangsu) and suspend and shake in 4.5mL sterile saline, which is 10 -1 Gradient (ten-fold dilution), take 0.5mL from the dilution and suspend and shake in 4.5mL sterile saline, which is 10 -2 Gradient (100-fold dilution), and so on, until diluted to 10 -6 gradient. Draw 100 μL from the dilutions of the 6 dilution gradients, spread them on the Nutrient Agar (NA) solid medium plate, prepare 2 copies in parallel, invert them, and culture them in a constant temperature incubator at 30°C for 24-36 hours, observe from time to time .
[0032] (2) Strain isolation and purification
[0033] Take out all the plates with colonies grown under the same sample, select a dilution plate with obvious single colonies and a moderate number, pick the colonies with different shapes on the plate to a ...
Embodiment 2
[0056] The generation of embodiment 2 Bacillus subtilis spores in NA medium
[0057] (1) Culture medium preparation
[0058] Liquid medium a: NB liquid medium: peptone 10g, beef extract powder 3g, sodium chloride 5g, agar 15g, distilled water 1L.
[0059] Liquid medium b: LB liquid medium: tryptone 10g, yeast extract powder 5g, sodium chloride 10g, agar 15g, distilled water 1L.
[0060] (2) Spore generation and expansion culture
[0061] Pick a single colony from the plate into a prepared centrifuge tube filled with 5mL of liquid medium a or b, culture at 30°C with shaking at 200rpm. Sampling started at 19h, the smear was dried naturally, fixed by flame heating, 5% malachite green staining solution was added dropwise, heated, and steamed 3-4 times within 30 seconds, do not boil, after cooling, rinse with tap water for 30 Seconds, add 0.5% sand yellow counterstaining solution, after 3 seconds, wash with water, air-dry, count under microscope, see results Figure 4 . Bacter...
Embodiment 3
[0063] Inorganic phosphorus dissolving ability of embodiment 3 bacillus subtilis CNBG-PGPR-1
[0064] (1) Preparation of culture medium
[0065] The composition of inorganic phosphorus liquid medium is glucose 10g, tricalcium phosphate 5g, calcium carbonate 0.1g, magnesium sulfate 0.5g, ammonium sulfate 0.5g, calcium sulfate 0.1g, ferric chloride 0.005g, water 1L.
[0066] (2) Inorganic phosphorus solubility
[0067] Take out the bacterial preservation tube of the strain CNBG-PGPR-1 frozen in the -80°C refrigerator, thaw it on ice until it becomes fluid, shake and mix well, pick up an appropriate amount of bacterial liquid with an inoculation loop, and line the three zones on the NA solid plate. Culture at 30°C for 24±2 hours, pick a single colony and purify it for 1-2 times and make identification and confirmation. After confirmation, pick a single colony and activate it in NA liquid medium, centrifuge to remove the NA medium, and weigh the bacteria sludge Suspend in an equ...
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