Bjerkandera adusta G14 and application thereof
A technology of tobacco tube bacteria and plant pathogenic bacteria, applied in the field of environmental microorganisms, can solve problems such as single function of strains, and achieve the effects of promoting growth, strong phosphorus-dissolving ability, and high development and utilization value
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Embodiment 1
[0028] Embodiment 1: pipe bacteria ( Bjerkandera adusta , G14) isolation, identification and preservation
[0029] 1.1 Medium and its preparation
[0030] PD medium: peel 200g of fresh potatoes, boil 1.1L of distilled water for 30min, filter through 4 layers of gauze to obtain potato liquid, add 0.05g of chloramphenicol to the potato liquid, and distilled water to dissolve to 1L;
[0031] PDB medium: add 20g / L glucose to PD medium;
[0032] PDA medium: add 20g / L agar powder to PDB medium;
[0033] Carbon source screening medium: on the basis of PD medium, 20g / L carbon source (glucose, maltose, sucrose, soluble starch, fructose) is added, and the pH is naturally added;
[0034] Nitrogen source screening medium: based on PDB medium, 1g / L nitrogen source (ammonium nitrate, ammonium chloride, ammonium sulfate, urea, peptone), natural pH;
[0035] Metal ion screening medium: on the basis of PDB medium, add 0.5mmol / L metal source (CuS , MnS , CaC , MgS , ZnS and FeC ...
Embodiment 2
[0045] Embodiment 2: pipe bacteria ( Bjerkandera adusta , G14) Determination of antibacterial properties
[0046] The plate confrontation method was used to determine the antibacterial activity of the strain against six kinds of plant pathogenic bacteria tested. First, all endophytic fungal strains and pathogenic bacteria are activated, and then in the ultra-clean workbench, punch holes on the fresh mycelium of the endophytic fungal strains and pathogenic bacteria edges activated in the PDA plate with a hole puncher with a diameter of 6mm, and respectively punch The bacterial cake obtained from the hole was inoculated on a PDA plate with a diameter of 90 mm. The inoculation point was on both sides of the medium, on the same diameter 20 mm from the edge of the plate, and three replicates were set up as the experimental group, and the pathogenic bacteria were only inoculated on the right side of the plate as the control group. , and set up 3 repetitions, and then place the exp...
Embodiment 3
[0047] Embodiment 3: pipe bacteria ( Bjerkandera adusta , G14) Determination of pro-proliferative properties
[0048] Endophyte Phosphorus Solubilization Screening:
[0049] The isolated and purified blueberry endophytic fungi were activated and cultured, and the activated endophytic fungi were picked (d=0.6cm) and inoculated on PKO inorganic phosphorus medium and Montina organic phosphorus medium respectively, and the inoculation After placing the last disposable culture dish in a constant temperature incubator at 28 °C for 72 hours, observe whether the transparent phosphorus-dissolving circle appears or not to determine whether the strain has phosphorus-dissolving effect, and measure and calculate the diameter of the phosphorus-dissolving circle D of the strain. Value and the ratio of the colony diameter d value, preliminarily judge whether the strain has phosphorus-solubilizing ability. The experiment shows that the D / d value of G14 in Montina medium is up to 1.7, which ...
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