Culture method of sinapine degradation bacteria capable of producing polyphenol oxidase
A technology of polyphenol oxidase and cultivation method, which is applied in the field of cultivation of polyphenol oxidase produced by sinapine-degrading bacteria, can solve the problems of bitter taste, affecting animal health, affecting the palatability of feed, etc., and achieve the secretion of polyphenol oxidase Improvement, simple and controllable culture conditions, good recovery and enzyme production effects
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Embodiment 1
[0022] The recovery medium consists of: bovine brain: 200.0g; bovine heart extract: 250.0g; soybean peptone: 13.0g; starch: 1.0g; NaCl: 5.0g; agar: 20.0g; distilled water: 1000ml. After mixing evenly, adjust the pH of the medium to 7. Sinapine-degrading bacteria were revived and cultured in the recovery medium at 27°C for 96 hours, and the culture solution was taken at 12, 24, 36, 48, 56, 72, 84, and 96 hours after the culture, and the mustard seed in the culture solution was determined. The concentration of alkali-degrading bacteria.
[0023] A single colony was picked from the brain-heart infusion agar recovery medium cultured for 96 hours and inoculated in the enzyme-producing medium, and cultured with shaking in a shaking incubator at 27°C for 6 days. The composition of the enzyme production medium is: NaNO 3 : 3.0g; K 2 HPO 4 : 1.0g; MgSO 4 ·7H 2 O: 0.5g; KCl: 0.5g; FeSO 4 : 0.01g; Tryptone: 13g; Sucrose: 1g; Sinapine: 0.4g; CuSO 4 : 0.5g; water: 1000mL. Take 30m...
Embodiment 2
[0025] Resuscitation medium composition: bovine brain: 250.0g; bovine heart extract juice: 200.0g; soybean peptone 15.0g; glucose 2.0g; NaCl: 4.0g; agar: 20.0g; 7.5. The sinapine-degrading bacteria were revived and cultured at 25° C. for 96 hours in the revival medium. The culture solution was taken at 12, 24, 36, 48, 56, 72, 84, and 96 hours after cultivation, respectively, and the concentration of sinapine-degrading bacteria in the culture solution was measured.
[0026] A single colony was picked from the brain-heart infusion agar recovery medium cultured for 96 hours and inoculated in the enzyme-producing medium, and cultured with shaking in a shaking incubator at 27°C for 6 days. The composition of the enzyme production medium is: NaNO 3 : 3.0g; K 2 HPO 4 : 1.0g; MgSO 4 ·7H 2 O: 0.5g; KCl: 0.5g; FeSO 4 : 0.01g; Tryptone: 13g; Sucrose: 1g; Sinapine: 0.6g; CuSO 4 : 0.5g; water: 1000mL. Take 30ml of the culture medium on the 2nd, 4th, and 6th day of culture, centrif...
Embodiment 3
[0028] The sinapine-degrading bacteria were revived and cultured at 27° C. for 96 hours in the resuscitation medium. Recovery medium composition: bovine brain: 200.0g; bovine heart extract juice: 250.0g; tryptone: 13.0g; sucrose: 1.0g; NaCl: 5.0g; agar: 20.0g; 7.2. The culture solution was taken at 12, 24, 36, 48, 56, 72, 84, and 96 hours after cultivation, respectively, and the concentration of sinapine-degrading bacteria in the culture solution was measured.
[0029] A single colony was picked from the brain-heart infusion agar recovery medium cultured for 96 hours and inoculated in the enzyme-producing medium, and cultured with shaking in a shaking incubator at 27°C for 6 days. The composition of the enzyme production medium is: NaNO 3 : 3.0g; K 2 HPO 4 : 1.0g; MgSO 4 ·7H 2 O: 0.5g; KCl: 0.5g; FeSO 4 : 0.01g; Tryptone: 13g; Sucrose: 1g; Sinapine: 0.8g; CuSO 4: 1g; Water: 1000mL. Take 30ml of the culture medium on the 2nd, 4th, and 6th day of culture, centrifuge at ...
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