A soil micro-ecological environment restoration method for eliminating continuous cropping obstacles
A technology for environmental remediation and continuous cropping obstacles, applied in the field of soil remediation, can solve the problems of unbalanced microbial population ratio, uneven distribution of soil nutrients, and ineffective decomposition of fertilizers, etc., to achieve the effect of preventing diseases and eliminating continuous cropping obstacles
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Embodiment 1
[0054] The preparation method of Pichia aumeri granule is as follows:
[0055] a), seed liquid preparation
[0056] On a sterile operating table, inoculate the Pichia aumerii strain into the seed medium, and cultivate the bacteria in a shaker at 28°C and 180rpm / min until the concentration of the bacteria reaches 10 8 CFU / mL, to obtain the seed solution;
[0057] b), fermentation culture
[0058] Add 5mL of the above seed liquid into the fermentation medium, cultivate in a shaker at 28°C and 180rpm / min, detect the number of bacteria in the fermentation bacteria, and wait until the number of bacteria reaches 10 10 Stop fermentation when CFU / mL, obtain Pichia aumeri yeast liquid;
[0059] c) air-drying the above-mentioned Pichia aumeri yeast liquid at 25° C. for 48 hours to obtain solid particles of Pichia aumeri yeast.
[0060] The pH of the described seed medium is 7.0, containing the following materials in parts by weight: 2 g of ammonium chloride, 5 g of sodium acetate, 0.1...
Embodiment 2
[0063] The preparation method of Hansenula anomaly granules is as follows:
[0064] a), seed liquid preparation
[0065] On a sterile operating table, inoculate the strain of Hansenula anomalies into the seed medium, and cultivate the bacteria in a shaker at 28°C and 180rpm / min until the concentration of the bacteria reaches 10 8 CFU / mL, to obtain the seed solution;
[0066] b), fermentation culture
[0067] Add 5mL of the above seed liquid into the fermentation medium, cultivate in a shaker at 28°C and 180rpm / min, detect the number of bacteria in the fermentation bacteria, and wait until the number of bacteria reaches 10 10 When the CFU / mL was reached, the fermentation was stopped, and the abnormal Hansenula yeast liquid was obtained;
[0068] c) Air-dry the above-mentioned Hansenula anomalies bacterial liquid at 25° C. for 48 hours to obtain solid particles of Hansenula anomalies.
[0069] The pH of the described seed medium is 7.0, containing the following materials in ...
Embodiment 3
[0072] The preparation method of the yeast granule of S. forticulata is as follows:
[0073] a), seed solution preparation
[0074] On a sterile operating table, inoculate the yeast strain of S. fumigatus in the seed medium, and cultivate the bacteria in a shaker at 28°C and 180rpm / min until the concentration of the bacteria reaches 10 8 CFU / mL, to obtain the seed solution;
[0075] b), fermentation culture
[0076] Add 5mL of the above seed liquid into the fermentation medium, cultivate in a shaker at 28°C and 180rpm / min, detect the number of bacteria in the fermentation bacteria, and wait until the number of bacteria reaches 10 10 When the CFU / mL is reached, the fermentation is stopped to obtain the yeast liquid of S. fumigatus;
[0077] c) air-drying the above yeast liquid of S. forticulata at 25° C. for 48 hours to obtain solid particles of S. forticulata.
[0078] The pH of the described seed medium is 7.0, containing the following materials in parts by weight: 2 g of...
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