Bacillus subtilis, edible fungus pre-picking treatment preparation and application of edible fungus pre-picking treatment preparation
A pre-harvest treatment technology for Bacillus subtilis, applied to improve the post-harvest storage quality of edible fungi, Bacillus subtilis, edible fungus pre-harvest treatment preparation field, can solve the pollution of Pseudomonas or Trichoderma, and the poor effect of preservatives , post-harvest quality deterioration and rapid deterioration, to achieve the effect of maintaining relative stability, reducing the level of membrane lipid peroxidation, and inhibiting fungal and bacterial diseases
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Embodiment 1
[0046] Example 1 strain screening
[0047] 1.1 Screening method:
[0048] (1) Preliminary screening: the above-mentioned soil samples or mushroom samples were gradiently diluted with sterile physiological saline to the soil bacterial suspension, and 10 -2 、10 -3 Dilution The dilution is spread on the beef extract peptone medium plate, cultured upside down at 37°C for 1-2 days, and the growth of the bacteria is observed every 12 hours. After the colony on the beef extract peptone plate grows, select the appropriate colony, use a sterilized toothpick to spot the selected colony on the primary screening medium plate, mark it, and place it at 37 ° C for 1-2 days.
[0049] (2) Re-screening: Use the plate confrontation method to judge whether the screened bacterial strains have inhibitory effect on the pathogenic fungus Trichoderma harzianum and white jade mushroom hyphae: pick the bacteria that are screened and place them in a dotted manner with the pathogenic fungus or white jad...
Embodiment 2
[0052] Identification of Example 2 bacterial strain B.subtilis NYB169
[0053] 2.1 Morphological identification results
[0054] Such as figure 1 As shown, the colonies grown by the strain B.subtilis NYB169 on the primary screening plate are about 3mm in diameter, roughly round, off-white, opaque, with a little wrinkle and rough edges. The strain showed blue-purple after staining, so it can be determined that the strain belongs to Gram-positive bacteria.
[0055] 2.2 Physiological and biochemical identification results
[0056] Physiological and biochemical experiments were carried out on B. subtilis NYB169, and the results are shown in Table 1. The strain can hydrolyze tyrosine and starch, and tyrosine crystals can be completely hydrolyzed to become transparent; methyl red (MR) test, peroxidation Hydrogenase test and indole test were both positive.
[0057] Table 1 Physiological and biochemical experiment results
[0058]
[0059] Note: "+" means positive, "-" means n...
Embodiment 3
[0067] The preparation of embodiment 3 edible fungi preharvest treatment preparation
[0068] 1. Cultivation and fermentation of strains
[0069] Fermentation medium: 0.06% potassium dihydrogen phosphate (KH 2 PO 4 ), 0.14% dipotassium hydrogen phosphate (K 2 HPO 4 ), 0.1% magnesium sulfate (MgSO 4 ), 0.06% yeast powder, 0.06% peptone, pH 7.0. Use water as solvent. The above-mentioned percentage content is a mass percentage.
[0070] Insert the strain B. subtilis NYB169 into the seed culture solution, cultivate overnight at 37°C and 150 r / min, and then inoculate the seed solution with the above-mentioned fermentation medium at an inoculation amount of 1% (v / v). In the Erlenmeyer flask, cultivate under the conditions of 37° C. and 150 r / min for 12 to 30 hours to obtain a fermentation broth. Separation of fermentation broth and bacteria by centrifugation or filtration.
[0071] 2. Preparation of preharvest preparations for edible fungi
[0072] After dissolving methyl ...
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