A kind of fertilizer making agent and its preparation method and application
A technology of composting and edible fungi, which is applied in the preparation of organic fertilizers, biochemical equipment and methods, applications, etc., can solve the problems of crop growth impact, environmental problems, and damage to the balance of soil flora, so as to achieve excellent fertilizer efficiency and improve fertilizer efficiency. Effect
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Embodiment 1
[0033] 1) Inoculate Cytophaga fermentans ATCC 19072, Cellulomonas flavigena ATCC 482, Butyrivibrio fibrisolvens ATCC 19171, Clostridium papyrosolvens ATCC 35413 in the cellulose-containing medium at a cell number ratio of 3:4:5:15, seal: seal: static culture , the culture temperature is 30°C, the culture pH is 3, and the culture is 5 days;
[0034] The cellulose-containing culture solution contains 2-7‰CaCO3, 3-7‰NaCl, 5-10‰cellulose, urea 1-4‰, peptone 1-3‰, yeast powder 0.5- 1.5‰, with water as solvent;
[0035] 2) Inoculate Bacillus megaterium ACCC 01742, Candida tropicalis ACCC 20199, and Phaneroderma chrysosporium ACCC30530 in PDA medium at a cell number ratio of 5:15:8, and culture them statically at a temperature of 35°C. Time 3d, in the described PDA culture medium, comprise 20% potato extract liquid by mass percentage, also comprise sucrose 20g / kg;
[0036] 3) Mix the cultures obtained in step 1) and step 2) uniformly at a volume ratio of 1:1, centrifuge, remove the...
Embodiment 2
[0040] 1) Inoculate Cytophaga fermentans ATCC 19072, Cellulomonas flavigena ATCC 482, Butyrivibrio fibrisolvens ATCC 19171, Clostridium papyrosolvens ATCC 35413 in the cellulose-containing medium at a cell number ratio of 17:25:10:28, seal and culture, culture temperature The temperature is 50°C, the culture pH is 10, and the culture time is 5 days;
[0041] The cellulose-containing culture solution contains 2-7‰CaCO3, 3-7‰NaCl, 5-10‰cellulose, urea 1-4‰, peptone 1-3‰, yeast powder 0.5- 1.5‰, with water as solvent;
[0042] 2) Mix and inoculate Bacillus megaterium ACCC 01742, Candida tropicalis ACCC 20199, and Phaneroderma chrysogenum ACCC30530 in PDA medium at a cell number ratio of 14:20:20, and culture them statically at a temperature of 35°C. Time 3d, in the described PDA culture medium, comprise 20% potato extract liquid by mass percentage, also comprise sucrose 20g / kg;
[0043] 3) Mix the cultures obtained in step 1) and step 2) uniformly at a volume ratio of 1:1, centri...
Embodiment 3
[0047] 1) Inoculate Cytophaga fermentans ATCC 19072, Cellulomonas flavigena ATCC 482, Butyrivibrio fibrisolvens ATCC 19171, Clostridium papyrosolvens ATCC 35413 in the cellulose-containing medium at a cell number ratio of 8.5:10:8.5:23. 40°C, culture pH 7, culture time 5 days;
[0048] The cellulose-containing culture solution contains 2-7‰CaCO3, 3-7‰NaCl, 5-10‰cellulose, urea 1-4‰, peptone 1-3‰, yeast powder 0.5- 1.5‰, with water as solvent;
[0049] 2) Inoculate Bacillus megaterium ACCC 01742, Candida tropicalis ACCC 20199, and Phaneroderma chrysosporium ACCC30530 in PDA medium at a cell number ratio of 13:19:18, and culture them statically at a temperature of 35°C. Time 3d, in the described PDA culture medium, comprise 20% potato extract liquid by mass percentage, also comprise sucrose 20g / kg;
[0050] 3) Mix the cultures obtained in step 1) and step 2) uniformly at a volume ratio of 1:1, centrifuge, remove the precipitate, and take the supernatant to obtain the fertilize...
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