Preparation method of dextran
A technology of dextran and preparation steps, which is applied in the field of preparation of dextran, can solve problems such as direct use, complicated operation, and inability to control molecular weight, and achieve the effects of quality assurance, simple operation, and simplified preparation process
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example 1
[0023] First, add 10g sucrose, 0.2g peptone, 0.2g disodium hydrogen phosphate, 0.03g potassium dihydrogen phosphate, 0.5g yeast extract, and 200mL deionized water to a 500mL petri dish in sequence, and mix them to make medium No. Leuconostoc membranosa; then weigh 0.1 g of Leuconostoc enterococcus enterica and inoculate it into the No. 1 medium above, and culture it with a shaker for 96 hours at 20°C, then centrifuge the culture solution at 5000 r / min for 30 minutes, Discard the supernatant to obtain Leuconostoc enterococcus cells for later use; then weigh 20g of peeled potatoes, cut them into pieces, put them into a beaker, add 400mL of deionized water to the beaker, heat to boiling, and keep warm for 20min , and then filter to get the filtrate, add 2g sucrose and 3g agar successively in the filtrate, mix and make No. 2 medium, cultivate Penicillium chrysogenum; then take 0.1g Penicillium chrysogenum and inoculate it in the above-mentioned No. 2 medium, At 25°C, after shaking...
example 2
[0026] First, add 15g sucrose, 0.3g peptone, 0.3g disodium hydrogen phosphate, 0.04g potassium dihydrogen phosphate, 0.6g yeast extract, and 250mL deionized water to a 500mL petri dish in sequence, and mix them to make medium No. Leuconostoc membranosa; then weighed 0.2g of Leuconostoc mesenteroides and inoculated it into the No. 1 medium above, at 23°C, cultured on a shaking table for 110h, then centrifuged the culture solution at 6000r / min for 35min, Discard the supernatant to obtain Leuconostoc enterococcus cells for later use; then weigh 25g of peeled potatoes, cut them into pieces, put them into a beaker, add 450mL of deionized water to the beaker, heat to boiling, and keep warm for 25min , then filter to get the filtrate, add 2.5g sucrose and 4g agar successively to the filtrate, mix and make No. 2 medium, cultivate Penicillium chrysogenum; then weigh 0.2g Penicillium chrysogenum and inoculate it into the above-mentioned No. 2 medium , at 28°C, after shaking with a shake...
example 3
[0029] First, add 20g sucrose, 0.4g peptone, 0.4g disodium hydrogen phosphate, 0.05g potassium dihydrogen phosphate, 0.7g yeast extract, and 300mL deionized water to a 500mL culture dish in sequence, and mix them to make medium No. Leuconostoc membranosa; then weighed 0.3g of Leuconostoc enterococcus enterica and inoculated it into the No. 1 medium above, at 25°C, cultured on a shaking table for 120h, then centrifuged the culture solution at 7000r / min for 40min, Discard the supernatant to obtain Leuconostoc enterococcus cells and set aside; then weigh 30g of peeled potatoes, cut them into pieces and put them into a beaker, add 500mL of deionized water to the beaker, heat to boiling, and keep warm for 30min , and then filter to get the filtrate, add 3g sucrose and 5g agar successively in the filtrate, mix and make No. 2 medium, cultivate Penicillium chrysogenum; then take 0.3g Penicillium chrysogenum and inoculate it in the above-mentioned No. 2 medium, At 30°C, after shaking w...
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