Candida drusei LSA and application thereof in ammonia-nitrogen degradation
A Candida and ammonia nitrogen degradation technology, applied in the field of microorganisms, can solve the problems of high operating costs, ammonia nitrogen, ammonia gas emissions, secondary pollution, etc., and achieve the effects of improving the environment in the house, improving safety, and increasing utilization
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Embodiment 1
[0027] Example 1. Isolation, purification and identification of Candida krusei LSA
[0028] 1. Isolation and purification of Candida krusei LSA
[0029] 1. Enrichment of ammonia nitrogen degrading bacteria
[0030] Take 20 g of chicken manure samples, inoculate them in a conical flask filled with 100 ml of sterilized distilled water (add sterilized glass beads to the bottle), shake at 30°C and 150 r / min for 30 minutes to fully break up the bacteria micelles, and let stand for 20 minutes. Take 5ml of the supernatant, inoculate it into a conical flask containing 100ml of enrichment medium, culture it with shaking at 30°C and 150r / min for 2 days, take 1ml of the culture medium and inoculate it again into a new enrichment medium, and repeat continuously Enriched for 10 generations.
[0031] 2. Screening, isolation and purification of ammonia nitrogen degrading bacteria
[0032] Draw 1ml of the enriched culture solution, and after 10 -1 After serial dilution, 200 μl was spread ...
Embodiment 2
[0043] Example 2, research on the function of Candida krusei LSA to degrade ammonia nitrogen
[0044] 1. Research on the degradation characteristics of Candida krusei LSA to high concentration ammonia nitrogen
[0045] 1. Preparation of Medium A
[0046] Medium A: Glucose was used as the sole carbon source, and the carbon source and (NH 4 ) 2 S0 4 The concentration of ammonia nitrogen is 1200mg / L, C / N is 10, and pH is 7.0.
[0047] 2. Pick a single clone of Candida krusei LSA, inoculate it in 100mL YPD liquid medium, and culture it with shaking at 30°C and 150r / min for 24-36h (to make the cell concentration in the culture system reach 8.0-9.0×10 8 cfu / mL), centrifuged at 4000rpm for 10min, collected the bacteria, and washed 3 times with sterile saline.
[0048] 3. Take the bacterial cells obtained in step 2 and resuspend them with sterile physiological saline to obtain a bacterial concentration of 8.0×10 8 cfu / mL bacterial suspension.
[0049] 4. Inoculate 0.1mL of the ...
Embodiment 3
[0074] Example 3, the influence of Candida krusei LSA on the amount of feces ammonia emission
[0075] 1. Pick a single clone of Candida krusei LSA, inoculate it in 100mL YPD liquid medium, and cultivate it with shaking at 30°C and 150r / min for 24-36h (to make the cell concentration in the culture system reach 8.0-9.0×10 8 cfu / mL), centrifuged at 4000rpm for 10min, collected the bacteria, and washed 3 times with sterile saline.
[0076] 2. Take the bacterial cells obtained in step 1 and resuspend them with sterile physiological saline to obtain a bacterial concentration of 8.0×10 8 cfu / mL bacterial suspension.
[0077]3. Take a large beaker (1L), put a small beaker in the large beaker (the small beaker is equipped with 20ml of absorption liquid; the absorption liquid is 0.01mol / L sulfuric acid solution), put 100g of fresh chicken manure in the large beaker The sample and 10ml of the bacterial suspension obtained in step 2 (using an equal volume of sterile normal saline as th...
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