High-conversion-rate xylitol strain and preparation method thereof
A high conversion rate, xylitol technology, applied in the biological field, can solve the problems of high cost of culture medium and increased production cost, and achieve the effects of simple and easy method, environmental protection and high conversion rate
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Embodiment 1
[0033] The screening of embodiment 1 bacterial strain
[0034] In the fermentation section of the xylose workshop, chromatographic detection found that the content of xylitol in the fermented liquid in a fermentation tank was more than 3 times higher than the usual detection, and samples were taken immediately for separation and cultivation. The xylose medium formula: xylose 10% by mass, heptahydrate 0.02 mass % of magnesium sulfate, 0.05 mass % of yeast extract, (NH 4 )H 2 PO 4 0.05% by mass, KH 2 PO 4 0.02% by mass, pH 5.8, if making a plate culture medium, add 2% by mass of agar (sterilized by an automatic pressure steam sterilizer at 120° C. for 20 minutes).
[0035] The fermenter is sampled, inoculated into xylose medium at a ratio of 5% by mass, cultivated in a 180rpm shaking incubator at 30°C for 12 hours, taking the culture solution and marking it on the xylose medium plate, and cultivating in a biochemical incubator at 30°C for 3- On the 4th day, high-quality c...
Embodiment 2
[0037] Embodiment 2 Fermentation experiment
[0038] Strain test tube culture: take out the preferred yeast slant from the refrigerator at 2-4°C, pick a single colony and inoculate it in a test tube containing 5ml of seed medium (5% wort medium, sterilized at 120°C for 15 minutes), Incubate in a biochemical incubator at 30°C for 24h (shake the test tube for 2-3 minutes every 4-8h).
[0039] Seed bottle culture: according to 10% inoculum, transfer the test tube seed solution to a 150ml Erlenmeyer flask containing 45ml seed medium (5% wort medium, sterilized at 120°C for 20 minutes) and cultivate for 12h (the culture condition is 30 °C, 180rpm).
[0040] 1000ml seed bottle cultivation: by 10% inoculum size, transfer the test tube seed solution to 450ml seed culture medium (components are 3 mass % of xylose, 1 mass % of glucose, 0.7 mass % of corn steep liquor powder, magnesium sulfate heptahydrate 0.02% by mass, adjust the pH value to 5.8, defoamer 0.005% by mass, sterilize at...
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