A kind of composite bacterial flora for degrading lignin wastewater and its preparation method
A technology of compound flora and lignin, applied in microorganism-based methods, biochemical equipment and methods, chemical instruments and methods, etc., can solve the problems of difficult biodegradation and low efficiency of biochemical treatment of pulp and paper wastewater.
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Embodiment 1
[0022]Pick Agrobacteriumsp., Bacillussp., Enterobacter.Cloacae., Gordoniasp., Pseudomonasputida. Bacteria (Pseudomonasstutzeri.) (isolated from the sludge at the outlet of the paper mill) six species of bacteria 1 ring: transfer them to 20mL nutrient solution (the composition is 1.5g / L beef extract, 1.0g / L L glucose, 5.5g / L tryptone, 3.0g / L yeast powder, pH 6.5, and the rest are water), each type of bacteria was cultured at 27°C for 2 days, and the cultured six kinds of bacteria Inoculate the container containing 300mL of proliferation medium at a volume ratio of 1:9 (bacteria and proliferation medium), culture at 27°C for 2 days, and finally centrifuge at 6000rpm for 15min to obtain the above six species The cells in the logarithmic growth phase of the bacteria were washed with normal saline, dried and refrigerated for later use. Among them, six different bacteria adopt different proliferation medium, the nutrient medium of Agrobacterium, rod-shaped bacteria and Enterobacter...
Embodiment 2
[0028] Pick six rings of bacteria respectively: Agrobacteriumsp., Bacillussp., Enterobacter.Cloacae., Gordoniasp., Pseudomonasputida. ), Pseudomonasstutzeri (Pseudomonasstutzeri.) (separated from the sludge at the outlet of the paper mill) were transferred to a nutrient solution containing 30mL (the composition of which was 2.0g / L beef extract, 1.5g / L glucose, 6.5g / L tryptone, 3.5g / L yeast powder, pH 7.5, and the rest are water), each type of bacteria was cultured at 30°C for 2 days, and the cultured six kinds of bacteria Inoculate them into containers containing 500mL of proliferation medium at a volume ratio of 1:10 (bacteria and nutrient solution), culture them at 35°C for 1 day, and finally centrifuge at 7000rpm for 10min to obtain the above six species The cells in the logarithmic growth phase of the bacteria were washed with normal saline, dried and refrigerated for later use. Among them, six different bacteria adopt different proliferation medium, and the nutrient med...
Embodiment 3
[0034]Pick six rings of bacteria respectively: Agrobacteriumsp., Bacillussp., Enterobacter.Cloacae., Gordoniasp., Pseudomonasputida. ), Pseudomonasstutzeri (Pseudomonasstutzeri.) (separated from the sludge at the outlet of the paper mill) were transferred to 25 mL of nutrient solution (the composition of which was 1.7 g / L beef extract, 2.0 g / L L glucose, 6.0g / L tryptone, 4.0g / L yeast powder, pH 7.0, the rest is water), each kind of bacteria was cultured at 30°C for 2 days, and then the cultured six kinds of bacteria Inoculate them into containers containing 400mL of proliferation medium at a volume ratio of 1:12 (bacteria and nutrient solution), culture them at 35°C for 2 days, and finally centrifuge at 7000rpm for 10min to obtain the above six species The cells in the logarithmic growth phase of the bacteria were washed with normal saline, dried and refrigerated for later use. Among them, six different bacteria adopt different proliferation media, among which the nutrient me...
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