Pseudomonas fluorescens and application thereof in promoting growth of poplar
A technology of Pseudomonas fluorescens and poplar, applied in the field of biological fertilizers and microbial fertilizers, can solve the problems of screening and application research that have not been reported, and achieve the effects of excellent strain resources, strong dissolution effect, and promotion of growth and development
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Embodiment 1
[0018] Example 1: JW-JS1 Phosphorus Solubilization Ability Test:
[0019] Phosphate Solubilizing Medium A: Glucose 10g, Ca 3 (PO 4 ) 3 5g, MgCl 2 5g, KCL 0.2g, MgSO 4 ·7H 2 O 0.25g, (NH 4 ) 2 SO 4 0.1g, distilled water 1000mL, pH 7.0.
[0020] Phospholytic medium B: with Ca 10 (PO 4 ) 6 (OH) 2 Instead of Ca in phosphate-dissolving medium A 3 (PO 4 ) 3 , the other components and contents are the same.
[0021] Inoculate the activated JW-JS1 strain into NB medium (3g of beef extract, 10g of peptone, 5g of sodium chloride, 1000mL of distilled water, pH 7.2-7.4), shake culture at 30°C for 18-24h to make seed liquid, and take 0.5ml of seed solution were inoculated in 100mL Erlenmeyer flasks containing 50mL of phosphate-dissolving medium A and 50mL of phosphate-dissolving medium B, and the same volume of blank seed solution was used as the control (CK), and each treatment was repeated 3 times, 30 °C, 180r / min shaking culture for 72h, the fermentation broth was centr...
Embodiment 2
[0023] Example 2: JW-JS1 optimal phosphorus solution test:
[0024] Using NBRIP (International Institute of Botany Phosphate Growth Medium, formulated with Phosphorus Solubilizing Medium A) as the basic medium, change the C source, N source, different C / N and environmental conditions. The results show that the optimum conditions for phosphorus solubilization are as follows: in a 100mL Erlenmeyer flask, glucose is used as carbon source, ammonium sulfate is used as nitrogen source, C / N is 80 / 1-100 / 1, liquid volume is 20-30mL, initial pH value is 7.0 ~7.2, inoculum size 3%~4%, temperature 28℃~30℃.
Embodiment 3
[0025] Embodiment 3: JW-JS1 greenhouse pot test:
[0026] After activating JW-JS1, use an inoculation loop to pick a small amount of bacteria and inoculate it into a 100mL Erlenmeyer flask containing 50mL of NB medium (3g of beef extract, 10g of peptone, 5g of sodium chloride, 1000mL of distilled water, pH 7.2-7.4), 29 Cultivate with shaking at 180r / min for 72h. Centrifuge the fermentation broth (4°C, 6000r / min) for 5min, rinse the bacteria with sterile normal saline for 2 to 3 times, then adjust the bacterial suspension with sterile normal saline (7~8×10 8 cfu / mL) to make bacterial agent. NL-895 cutting seedlings and black poplar seedlings (60 days old) were inoculated respectively, and the same amount of sterile saline was used as the control, and the inoculation volume was 15 mL / plant for cutting seedlings and 5 mL / plant for seedlings. 6 replicates per treatment were placed in the greenhouse for unified management, the light was 12h / day, and watering was timely.
[0027]...
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