Method for promoting rapid propagation of arbuscular mycorrhizal fungal spores
A technology of arbuscular mycorrhizal fungi and spores, which is applied in the field of microbial cultivation, can solve the problems of being easily contaminated by miscellaneous bacteria, low spore content, and low quality of bacterial preparations, and achieves avoidance of miscellaneous bacteria pollution, high spore content, and high quality of bacterial preparations. Good results
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Embodiment 1
[0033] The method for promoting the rapid propagation of arbuscular mycorrhizal fungus spores in this embodiment is carried out in the following steps:
[0034] (1) Mix vermiculite, zeolite, pumice and peat into a substrate at a volume ratio of 3:3:3:1, dry heat sterilization at 160°C for 4 hours, and obtain arbuscular mycorrhizal fungus culture substrate, whose basic physical and chemical properties are as follows : Organic matter 14.0g / kg, total nitrogen 1.16g / kg, total potassium 1.11g / kg, total phosphorus 30mg / kg.
[0035] (2) Select corn, marigold and clover as host plants, select plump and uniform corn seeds, and adopt a concentration of 1% H 2 o 2 Disinfect for 10 minutes, then rinse with distilled water and soak for 4 hours in an incubator at 28°C to accelerate germination; the concentration of clover and marigold seeds is 1% H 2 o 2 After 10 minutes of disinfection, the seeds can be sown. Use a flower pot with a diameter of 21 cm and a height of 18 cm as a cultivat...
Embodiment 2
[0042]The difference between this embodiment and Example 1 is that in step (3), it is set to simultaneously add spermidine and arbuscular mycorrhizal fungi to treat, only inoculate arbuscular mycorrhizal fungi, only add spermidine to treat, and not add arbuscular mycorrhizal fungi. Mycorrhizal fungus and spermidine are handled, altogether 4 are handled; In step (4), spermidine is pressed 0.25mg / m 3 Spray evenly on the bacterial agent, other steps and parameters are the same as the first embodiment.
[0043] Determination of mycorrhizal infection rate: 1) After cleaning the root system, cut it into 1-2cm long pieces and put them in a beaker; 2) Add 10% KOH solution, treat at 90°C for 40min, pour off the liquid Finally, wash the root system with distilled water; 3) Add 2% lactic acid or 2% HCl, treat at 90°C for 20 minutes, and pour off the liquid; 4) Add 0.05% trypan blue dye solution, dye at 90°C for 30 minutes, cool for at least 30min; 5) Pour off the dye solution, add a dec...
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