Culture medium capable of efficiently screening xanthine oxidase producing bacteria
A technology of xanthine oxidase and culture medium, which is applied in the field of culture medium for efficiently screening xanthine oxidase-producing bacteria
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example 1
[0039] 10 grams of peptone, 5 grams of yeast powder, 10 grams of sodium chloride, 1000 ml of water, adjust the pH to 7.00 ± 0.05 with 0.1 mol / liter hydrochloric acid or sodium hydroxide solution, add 0.2 grams of hypoxanthine, add 20 grams of agar, Sterilize at 120 degrees for 15 minutes. When the temperature drops below 45 degrees, add phenol (solution) to a final concentration of 0.1 g / L, mix well, and pour it into a flat plate (about 45 mm in diameter). The number of repetitions is 3.
[0040] After the plate is solidified, take 0.1 ml of the sample (soil dilution) and spread it on the plate, cultivate it at 30 degrees for 4 days, and see that colonies grow on the plate, pick the colonies and induce and detect the enzyme activity on the double screening medium. The number of colonies and the positive rate were counted, and the results are shown in Table 1.
example 2
[0042] 10 grams of peptone, 5 grams of yeast powder, 10 grams of sodium chloride, 1000 ml of water, adjust the pH to 7.00 ± 0.05 with 0.1 mol / L hydrochloric acid or sodium hydroxide solution, add 2 grams of hypoxanthine, add 20 grams of agar, Sterilize at 120 degrees for 15 minutes. When the temperature drops below 45 degrees, add phenol (solution) to a final concentration of 1 g / L, mix well, and pour it into a flat plate (about 45 mm in diameter). The number of repetitions is 3.
[0043] After the plate is solidified, take 0.1 ml of the sample (soil dilution) and spread it on the plate, cultivate it at 30 degrees for 4 days, and see that colonies grow on the plate, pick the colonies and induce and detect the enzyme activity on the double screening medium. The number of colonies and the positive rate were counted, and the results are shown in Table 1.
example 3
[0045] 10 grams of peptone, 5 grams of yeast powder, 10 grams of sodium chloride, 1000 ml of water, adjust the pH to 7.00 ± 0.05 with 0.1 mol / L hydrochloric acid or sodium hydroxide solution, add 5 grams of hypoxanthine, add 20 grams of agar, Sterilize at 120 degrees for 15 minutes. When the temperature drops below 45 degrees, add phenol (solution) to a final concentration of 2 g / L, mix well, and pour it into a flat plate (about 45 mm in diameter). The number of repetitions is 3.
[0046] After the plate is solidified, take 0.1 ml of the sample (soil dilution) and spread it on the plate, cultivate it at 30 degrees for 4 days, and see that colonies grow on the plate, pick the colonies and induce and detect the enzyme activity on the double screening medium. The number of colonies and the positive rate were counted, and the results are shown in Table 1.
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