Aspergillus awamori and its microbe inocula and application thereof
A technology of Streptomyces pseudogreyishus and microbial agents, applied in the field of preventing and treating tomato seedling blight, can solve the problems of environmental pollution, economic loss of agricultural production, etc., increase stem diameter, reduce morbidity, prevent The effect of excellent control rate
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Embodiment 1
[0030] Preparation of bacteria.
[0031] Explanation of the materials involved: The tomato variety tested is Zheza 205; the Streptomyces pseudogriseolus strain nmg4 (Streptomyces pseudogriseolus), which is an antagonistic strain to Streptomyces pseudogriseolus, was isolated and preserved in our laboratory. Damping-off pathogenic strain Pythium ultima ( Phthium ultinum , ACCC36075, hereinafter referred to as 36075) was purchased from China Agricultural Microorganism Culture Collection Center.
[0032] Streptomyces pseudogriseolus nmg4 adopts Actinomyces No. 1 Gaoshi culture medium, and PDA medium is used for the cultivation of the pathogenic bacteria of Streptomyces pseudogiseolus.
[0033] Substrate material and co-cultivation substrate: conventional substrate raw materials are respectively fermented and decomposed rice wine distiller's grains and mushroom residues after cultivation of Flammulina velutipes; semi-fermented and decomposed distiller's grains and mushroom resi...
Embodiment 2
[0037] Seedling comparison test.
[0038] Tomato seeds were selected for the antagonistic substrate seedling cultivation experiment. Three treatments were set up in the experiment: conventional substrate inoculated with pathogenic bacteria, antagonistic bacteria co-cultivated substrate, and antagonistic bacteria co-cultured substrate inoculated with pathogenic bacteria. A 25-hole seedling tray was used, and the experiment was repeated 3 times. Before sowing, mix the co-cultivation antagonistic matrix and conventional matrix materials, perlite and vermiculite in a ratio of 8:1:1, and then add compound fertilizer (15-15-15) and 2% of The 10-fold diluted pathogenic bacteria culture solution was mixed evenly with the substrate in proportion. Seeds were germinated in an incubator at 28°C, and sown in plug trays in time after germination. The seedlings were tested regularly, and the incidence rate was recorded. After the test, 10 plants were randomly selected for each repetition ...
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