Alcaligenes faecalis, method for preparation of desulfurization deodorant from the same and application
A technology of Alcaligenes faecalis and deodorant, which is applied in the field of Alcaligenes faecalis and its application in environmental deodorization, and can solve the problems of difficulty in obtaining high-density bacteria, increasing the cost of deodorization reaction, and long metabolic time of strains, etc. no secondary pollution, solve the problem of odor, and quickly deodorize
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Embodiment 1
[0035] Example 1 Isolation and identification of Alcaligenes faecalis M50-B1 strain
[0036] 1. Isolation of strains
[0037]The source of isolation comes from the sawdust on the surface of the compost biofilter. The sample was inserted into 100ml heterotrophic sulfur oxidizing bacteria screening medium according to the inoculation amount of 5% (V / V), and placed in a constant temperature shaker for cultivation. The temperature was controlled at 30°C, 120r / min, regularly (7 days) transferred to fresh medium to continue enrichment. After 21 days of acclimatization, the sulfur oxidation efficiency of the samples after 3 consecutive passages was measured, and it was obtained that the metabolic efficiency reached more than 90%. The obtained enriched culture solution was serially diluted and spread onto a solid plate of heterotrophic sulfur oxidizing bacteria culture medium, cultured at 30°C for 7 days, and single colonies were picked and streaked for separation and purification t...
Embodiment 2
[0047] Embodiment 2 Preparation and use of liquid desulfurization and deodorant
[0048] (1) Under aseptic conditions, pick 1-2 rings of Alcaligenes faecalis M50-B1 strain stored in a glycerol tube at -80°C, and streak on a fresh heterotrophic sulfur-oxidizing bacteria solid medium plate. Lines were cultured at 28°C for 3 days.
[0049] (2) Pick one ring of the culture from (1) and place it in 150 ml of heterotrophic sulfur-oxidizing liquid bacterial culture medium at 28°C for shaking culture on a shaker, and culture for 26 hours to obtain a seed liquid. Add 5L of water to a 7L small fermenter, and add 15g of beef extract, 45g of peptone, 15g of yeast extract, Na 2 HPO 4 12H 2 O 10g, NaCl 15g, 1mol / L hydrochloric acid to adjust the pH to 7.0, sterilize at 121°C for 20min. When the temperature of the culture medium drops to 28°C, inoculate the seed liquid in the fermenter at a volume ratio of 2%, at a temperature of 28°C, with an air flow of 5 L / min, and a stirring speed of...
Embodiment 3
[0052] Embodiment 3 Preparation and use of solid desulfurization deodorant
[0053] (1) Strain activation: Under sterile conditions, pick 1-2 rings of Alcaligenes faecalis M50-B1 strain stored in a glycerol tube at -80°C, and culture them on fresh heterotrophic sulfur oxidizing bacteria solid Streak on the basal plate and incubate at 30°C for 2 days.
[0054] (2) Pick one ring of the culture from (1) and culture it on a shaker at 30° C. in 50-150 mL of heterotrophic sulfur-oxidizing liquid bacterial culture medium, and culture it for 25 hours to obtain a seed liquid.
[0055] (3) Inoculate the above-mentioned seed liquid into a fermenter containing freshly sterilized heterotrophic sulfur-oxidizing liquid bacterial culture medium at a volume ratio of 5%, and ferment and cultivate at 28°C with a tank pressure of 0.05Mpa and an air flow of 80L / min 1. The stirring speed is 150r / min, add 40mL foam enemy as a defoamer, take a sample every two hours, measure the absorbance at 600nm ...
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