Aspergillus niger with dual-function of phosphorus-dissolving and bio-control as well as microorganism preparation and application
A microbial preparation, dual-function technology, applied in the field of Aspergillus niger and microbial preparations, can solve problems such as uncommon, and achieve the effect of strong dephosphorization ability
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Embodiment 1
[0024] Example 1: Preliminary Screening of Phosphorus Solubilizing Microorganisms
[0025] Collect the soil with mild wheat head blight, weigh 10g, put it in a triangular flask filled with 100mL of sterile water, shake it at 28°C and 180rpm for 20min, and let it stand for 10min to obtain a soil suspension. Dilute the suspension to a suitable concentration and spread it on the primary screening medium plate of phosphate-solubilizing bacteria, culture it upside down at 28°C, observe every 2 days, pick out the colonies with phosphorus-dissolving circles, and re-inoculate on the phosphate-solubilizing bacteria by streaking method. Bacteria primary screening medium plate for purification, repeated 2 to 3 times, purified to a single colony. Inoculate the strains with phosphorus-dissolving effect after purification on the primary screening medium plate of phosphate-solubilizing bacteria, and culture them upside down at 28°C for 7 days, and measure the diameters of phosphorus-dissolvi...
Embodiment 2
[0029] Embodiment 2: shake flask re-screening of phosphorus-solubilizing microorganisms
[0030] Test strains: 5 strains of phosphate-solubilizing bacteria obtained from preliminary screening.
[0031] Prepare re-screening medium for phosphate-solubilizing bacteria, pack in 250mL Erlenmeyer flasks, 50mL per bottle, and sterilize for later use. After activating the 5 strains of phosphate-solubilizing bacteria obtained from the preliminary screening, use a slant to make a uniform 5mL bacterial suspension, inoculate 1mL bacterial suspension into each triangular flask, inoculate 3 triangular flasks, and make 3 non-inoculated controls at the same time, Place them on a shaker (130r / min) at 28°C for 7 days and then set them aside for later use. Add phosphorus-free activated carbon to the fermentation broth for decolorization and centrifugation for 15min (8000r / min), and keep the supernatant. Take 10mL of the supernatant into a 50mL volumetric flask, dilute to 30mL with water, add 2...
Embodiment 3
[0037]Embodiment 3: the identification of phosphate solubilizing bacteria HY30
[0038] Colony morphology: It grows fast on PDA medium. After 24 hours, colonies appear, and after 72 hours, spores are abundant; the colonies are black and velvety, with a slightly raised center, and the opposite side of the colonies is slightly yellow. Under the microscope, the flora is dark brown with well-developed hyphae. The conidia head is like a "chrysanthemum" with two layers of spore stalks. The conidia are spherical and black or dark brown. figure 1 and figure 2 These are the morphology of HY30 on the PDA plate and under the microscope.
[0039] Molecular biology identification of HY30 strain: The 18SrDNA of HY30 was detected by molecular biology method
[0040] Sequences were blasted against the GenBank database. Combining the results of colony morphology and 18SrDNA comparison, the applicant determined that the HY30 strain was Aspergillus niger. The strain was deposited in the Chi...
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