A kind of high-efficiency erosion bacterium Serratia liquefaction nlx-15 of silicate rock and its application
A technology of Serratia and silicate, applied in the field of microorganisms, to achieve the effects of accelerated erosion into soil, strong erosion ability, and good application and development prospects
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Embodiment 1
[0021] The acquisition and identification of embodiment 1 bacterial strain:
[0022] Collect the colonies in the biological crust on the bare rock surface of silicate rock (Jiangxi Lushan rock mining area), and use the dilution plate method to screen the medium (5.0g sucrose, 2.0gNa 2 HPO 4 , 0.5gAlSO 4 ·7H 2 O, 0.005g FeCl 3 , 0.1 g CaCO 3 , 1.0 Silicate rock slag (cleaned Lushan rock mining area rock, polished to rock powder, 200 mesh sieve, main chemical composition: 73.8% SiO 2 , 13.4% Al 2 o 3 , 9.9%K 2 (2), 18g agar powder, 1000mL distilled water) were cultivated for about 48 hours, single colonies were picked, streaked and purified repeatedly, and the resulting bacterial strains were respectively inoculated on the slant of beef extract peptone solid medium, stored in a refrigerator at 4°C to obtain pure bacterial strains. The main biological characteristics of the strain: cultured at 28°C on beef extract peptone solid medium, the thalline is straight rod-shaped,...
Embodiment 2
[0024] The silicate rock dissolution ability of embodiment 2 bacterial strains:
[0025] Use an inoculation loop to inoculate a small amount of pure Serratia liquefaction strain NLX-15 into a 250mL Erlenmeyer flask filled with 50mL screening medium (the medium is the same as above, without adding agar powder), culture at 28°C and shake at 180r / min for 72h, and obtain Activate the bacteria.
[0026] Take 2.0mL of bacterial suspension cultured for 24h (6.0×10 6 cfu mL -1 ) into 100mL potassium-deficient medium (10g sucrose, 2.0g NaHPO 4 , 0.5g AlSO 4 ·7H 2 O, 0.1g NaCl, 0.5g yeast extract, 1000mL deionized water, adjust the pH to 7.2-7.4. ) and 0.2g of silicate rock powder in a 250mL Erlenmeyer flask, another 1mL of high-temperature inactivated bacterial suspension at 121°C was inserted into the culture medium as a control, and three parallel samples were made for each treatment method. Culture at 28°C with shaking at 180rpm. Take 5.0mL of the fermentation broth cultured ...
Embodiment 3
[0035] The influence of embodiment 3 bacterial strains on plant growth
[0036] After the bacterial strain is activated (the method is the same as in Example 2), according to 100mL·kg -1 Mix in the spraying matrix (woodland soil, add humic acid organic fertilizer 25%, silicate rock powder (200 mesh sieve) 4%, spraying wood fiber 0.3%, water retaining agent 0.3%, greening spraying adhesive 0.03% ), and the control was mixed with the same volume of culture medium in the spraying substrate, and carried out a pot test (pot diameter 17cm, depth 15cm). Place them in a greenhouse at 25°C. After the seeds germinate, keep the three best seedlings in each pot, and measure the height and biomass of the plants after 3 months. , and each experiment was done in 3 parallel treatments.
[0037] Plant height is one of the most basic indicators in the investigation of plant morphology, which refers to the distance from the root neck to the top of the plant. It can be seen from Table 2 that t...
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