Culture method for improving adsorption capacity of zygosaccharomyces rouxii heavy metal cadmium
The invention relates to a technology for the adsorption capacity of Ruchella yeast, which is applied in the cultivation field of improving the adsorption capacity of the heavy metal cadmium of Russellii, and can solve the problems such as the pollution of the treated liquid.
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Embodiment 1
[0018] Step 1. Add 10g of yeast extract, 18g of peptone, 20g of glucose and 5% sodium chloride to 1000mL of distilled water; slowly heat up until it is completely dissolved to obtain a liquid medium, then use 0.1mol / L of hydrochloric acid and hydrogen Adjust the pH of the medium with sodium oxide solution to 6.0, and sterilize at 115°C for 20 minutes.
[0019] Step two: inoculate the liquid seeds of the activated yeast Lu's yeast into the medium obtained in step one. The culture conditions of the controlled shake flask were: constant temperature 28°C, shaker rotation speed 180rpm, liquid volume 100ml / 500ml, inoculation volume 4%, culture for 24h.
[0020] In step three, the fermentation broth obtained in step two was centrifuged at 4000 rpm for 20 minutes to collect the bacteria, the surface medium was washed, and then freeze-dried to prepare a powder.
Embodiment 2
[0022] Step 1. Add 10g of yeast extract, 22g of peptone, 20g of glucose and 10% potassium chloride into 1000mL of distilled water successively; slowly warm up until it is completely dissolved to obtain liquid culture medium, and then use 0.1mol / L hydrochloric acid and hydrogen Adjust the pH of the medium with sodium oxide solution to 6.2, and sterilize at 115°C for 20 minutes.
[0023] Step two: inoculate the liquid seeds of the activated yeast Lu's yeast into the medium obtained in step one. The culture conditions of the fermenter were: constant temperature 28°C, rotation speed 300 rpm, liquid loading coefficient 0.6, inoculation amount 10%, ventilation rate 1 vvm, and culture for 48 hours.
[0024] In step three, the fermentation broth obtained in step two is centrifuged at 5000 rpm for 10 minutes to collect the bacteria, the surface medium is washed, and freeze-dried to prepare a powder.
Embodiment 3
[0026] Step 1. Add 10g of yeast extract, 20g of peptone and 200g of glucose to 1000mL of distilled water successively; slowly increase the temperature until it is completely dissolved to obtain a liquid medium, then adjust the medium with 0.1mol / L hydrochloric acid and sodium hydroxide solution pH to 6.0, sterilize at 115℃ for 20min.
[0027] Step two: inoculate the liquid seeds of the activated yeast Lu's yeast into the medium obtained in step one. The culture conditions of the controlled shake flask were: constant temperature of 30°C, shaker speed of 160rpm, liquid volume of 100ml / 500ml, inoculation volume of 4%, and culture for 42 hours.
[0028] In step three, the fermentation broth obtained in step two was centrifuged at 6000 rpm for 10 minutes to collect the bacteria, the surface medium was washed, and freeze-dried to prepare a powder.
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