Production method of glucose oxidase for feeding
The technology of a glucose oxidase and production method, which is applied in the field of feed processing, can solve problems such as difficult control of fermentation conditions, and achieve the effects of easy control of fermentation conditions, high activity, and less contamination of miscellaneous bacteria
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Embodiment 1
[0031] The production method of glucose oxidase for feed is as follows:
[0032] The first step, strain activation: take out the slant of Penicillium specificum with high glucose oxidase production, streak and inoculate it on a PDA (potato dextrose agar medium, the same below) solid culture plate with a diameter of 10 cm, and cultivate it at 28°C for 72 hours , then spread and inoculate on a PDA solid culture plate with a diameter of 20 cm, and culture at 28°C for 48 hours to obtain activated Penicillium specificum.
[0033] Preparation of potato agar medium: 200g of peeled potatoes, cut into small pieces, add boiled juice for 30min, filter with gauze, add 15g of agar to the filtrate, continue heating and stirring until the agar dissolves, then add 20g of glucose, add distilled water to 1000mL, 115 Sterilize at ℃ for 20 minutes, spread the plates for later use;
[0034] The second step, primary seed culture: After the primary liquid seed medium is sterilized at 115°C for 20 m...
Embodiment 2
[0038] The production method of glucose oxidase for feed is as follows:
[0039] The first step, strain activation: take out the slant of the preserved high-yield Penicillium specificum of glucose oxidase, streak and inoculate it on a PDA solid culture plate, cultivate it at 32°C for 96 hours, and then spread and inoculate it on a PDA solid with a diameter of 20cm Culture plates were cultured at 32°C for 96 hours.
[0040] The preparation of the potato agar medium: cut 200 g of peeled potatoes into small pieces, add boiled juice for 30 min, filter through 8 layers of gauze, add 15 g of agar to the filtrate, continue heating and stirring until the agar is dissolved, then add 20 g of glucose, and add distilled water to 1000 mL , sterilized at 115°C for 20 minutes, spread on plates for later use;
[0041]The second step, primary seed culture: After the primary liquid seed medium is sterilized at 115°C for 20 minutes, transfer the activated Penicillium inoculum to the primary see...
Embodiment 3
[0049] The first step, strain activation: take out the slant of the preserved Penicillium specificum with high glucose oxidase production, streak and inoculate it on a PDA solid culture plate with a diameter of 10 cm, cultivate it at 30°C for 72 hours, and then spread and inoculate it on a PDA solid culture plate with a diameter of 10 cm. A 20cm PDA solid culture plate was cultured at 30°C for 72h.
[0050] The preparation of the potato agar medium: cut 200 g of peeled potatoes into small pieces, add boiled juice for 30 min, filter through 8 layers of gauze, add 15 g of agar to the filtrate, continue heating and stirring until the agar is dissolved, then add 20 g of glucose, and add distilled water to 1000 mL , sterilized at 115°C for 20 minutes, spread on plates for later use;
[0051] The second step, primary seed culture: After the primary liquid seed medium is sterilized at 115°C for 20 minutes, transfer the activated Penicillium inoculum to the primary seed medium, and th...
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