White and mycorrhizal fungi and their application
A mycorrhizal fungus and mycelium technology, applied in the fields of application, fungi, and chemicals for biological control, etc., can solve problems such as difficult to meet cultivation needs, slow propagation speed of rhizome ramets, susceptibility to pathogenic bacteria, etc. To achieve the effect of protection and regeneration and sustainable utilization, the cultivation effect is remarkable, and the growth cycle is shortened
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Embodiment 1
[0038] Identification of strains
[0039] 1. Extraction of fungal DNA:
[0040] The fungi used for molecular identification were inoculated on PDA medium and cultured at 25°C in a dark room for 2 weeks. When the diameter of the fungal colony was 3 to 5 cm, the hyphae on the surface of the colony could extract DNA.
[0041] DNA extraction was carried out according to the instructions of the Fungal DNA Extraction Kit (E.Z.N.ATM Fungal DNA Kit, Omega Bio-Tek, Doraville, Georgia, USA). The specific steps are as follows:
[0042] 1) Scrape 50-100mg of mycelium into a sterilized mortar, add liquid nitrogen to freeze, immediately grind into powder, and scrape the ground hyphae into a sterilized 1.5mL Eppendorf tube.
[0043] 2) Add 800μL of Buffer FG1 buffer to the Eppendorf tube, vortex and mix well, then in a water bath at 65°C for 10 minutes, and invert and mix twice during the water bath.
[0044] 3). Then add 140μL Buffer FG2, vortex and mix well, and centrifuge at 13300r / min for 10min at ...
Embodiment 2
[0080] 1. First use PDA solid medium to activate the white and mycorrhizal fungus strains at a culture temperature of 26±2℃, cultivate in the dark for 7-15 days, then pick several small pieces from the edge of the formed colony and inoculate them into the liquid medium Carry out dark culture on a shaker, the rotating speed of the shaker is 100r / min~150r / min, the culture temperature is 26℃±2℃, and the culture is dark for 10-20 days. After the culture, the obtained mycorrhizal fungus mycelium can be used directly. It can also be used after crushing with a soymilk machine.
[0081] 2. The effect of liquid medium on mycorrhizal fungus mycelium
[0082] The liquid culture medium is composed of glucose, inorganic salts and natural extracts. The amount of glucose added is 15g / L-40g / L, and the inorganic salt is MgSO 4 ·7H 2 O and KH 2 PO 4 The natural extract is one of potato extract, wheat bran extract, and oat extract.
[0083] 1) For MgSO in liquid medium 4 ·7H 2 Experiment with the amou...
Embodiment 3
[0107] The inventor took 200 white and white seeds and divided them into two groups. In 1 group, white and white seeds and white and mycorrhizal fungal mycelium were used as materials according to the method in Example 2 to produce white and white seeds and white and mycorrhiza. After the symbiotic mixture of fungi, they were directly sown in the field. In the second group, the seeds were sown directly in the field. At the 5th week after sowing, the first group began to germinate. The seed germination in 5-12 weeks was measured as shown in Table 5. Show:
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