Special culture medium for isolating endophytic trichoderma fungi as well as preparation method and application thereof
A culture medium and a technology for growing Trichoderma, applied in the field of microorganisms, can solve the problems of difficulty in counting and picking colonies, dispersion of Trichoderma mycelium, and few isolated species, and achieve the effects of obvious colony characteristics, easy separation and low price.
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Embodiment 1
[0024] This example provides a special medium for isolating endophytic Trichoderma fungus, and its components include potato, glucose, agar powder, chloramphenicol, streptomycin sulfate, Bengal red, pentachloronitrobenzene and water. The preparation method of this special medium is briefly described as follows:
[0025] 1) Prepare PDA medium
[0026] PDA medium: potato (peeled) 200g, glucose 20g, agar 12g, add sterilized water (or distilled water) to 1000mL, natural pH value.
[0027] The specific preparation process of PDA medium: Peel 200g of potatoes and cut them into small pieces, put them into 1000mL of water and boil until the potatoes become soft and not rotten, then filter with 8 layers of gauze, and pour the filtrate back into the pot Add agar and glucose, stir evenly and replenish water to 1000mL, and finally divide into 150mL Erlenmeyer flasks for later use.
[0028] 2) Add bacteria inhibitors
[0029] Add an appropriate amount of miscellaneous bacteria inhibitor...
Embodiment 2
[0032] This example provides a conventional method for isolating and cultivating endophytic Trichoderma using the special culture medium for isolating endophytic Trichoderma described in Example 1.
[0033] Firstly, the tissue samples such as plants, leaves and rhizomes of different crops (vegetation) collected were rinsed with tap water, then soaked in 75% ethanol for 5 minutes, then transferred to 2% sodium hypochlorite for 5 minutes, and finally rinsed with sterile water 3 to 5 times, thoroughly disinfect the surface. Afterwards, put an appropriate amount of sterilized plant or tissue samples into a high-speed crusher to crush them into pulp, use the flat plate smear method, take the juice (or add 30mL sterilized water after appropriate dilution) and evenly apply it on the special-purpose powder described in this embodiment. On the medium plate, use 0.2mL of medium per plate of 25mL, repeat 3 times for each treatment, and then place it in a mold incubator at 25°C for 3-5 da...
Embodiment 3
[0035]This example provides a comparison of the effects of using different culture media to isolate endophytic Trichoderma. In this example, three commonly used culture media were selected as controls (medium number 1-3), see Table 1 for details. According to relevant documents and preliminary experiments, utilize the conventional medium No. 1 of separating endophytic fungus, Martin's medium No. 2 and the selective medium 3 of Trichoderma in the separation soil and the medium 4 of the present invention's development, adopt tissue disinfection and smear method for the isolation of endophytic Trichoderma.
[0036] Table 1 The results of the determination of the effect of different culture media on the separation of endophytic Trichoderma fungus
[0037]
[0038] The results (table 1) of the effect measurement of different culture media for separating endophytic Trichoderma fungus show that medium 4 has a significant inhibitory effect on two kinds of miscellaneous bacteria, b...
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