Acid-resistant bacterial cellulose high-yielding strain and method for preparing edible bacterial cellulose with same
A technology of bacterial cellulose and bacterial strains, which is applied in the field of bacterial cellulose high-yielding bacteria and edible bacterial cellulose prepared by the bacterial strain, can solve the problems of few research reports on the fermentation process of bacterial cellulose high-yielding bacteria, and achieve low cost and high yield. High efficiency and good quality effect
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Embodiment 1
[0021] Example 1: Screening, isolation and identification of Gluconacetobacter xylinum JX1a
[0022] Collect Hainan coconut milk, let it ferment naturally (that is, self-ferment under natural conditions) for 15 days, draw 1ml into a 10ml test tube, and then add 9ml sterile water to make 10 -1 Concentration of bacterial suspension, diluted sequentially, respectively from 10 -2 、10 -3 Draw 200 μl of the concentration gradient dilution solution and spread it evenly on the plate. Make three controls for each concentration gradient, and place it in a 30°C incubator to observe the cultivation situation. After 4 days of cultivation, pick the colony that grows well, distributes evenly, and produces a transparent circle. All single colonies were inoculated on solid slant medium, and incubated at 30°C for 24-48 hours. After a thick lawn grows on the slant, pick a ring of bacteria from the slant and inoculate it in 10ml of fermentation broth and incubate at a constant temperature of 30...
Embodiment 2
[0030] Embodiment 2: the preparation method of edible bacterial cellulose
[0031] Inoculate the slant seeds into a 10mL test tube (seed medium glucose 2%, yeast extract 0.5%, K 2 HPO 4 0.2%, MgSO 40.15%, ethanol 2%), cultured in a constant temperature incubator at 30°C for 24 hours, and after the fibrous membrane grew on the surface, it was transferred to 100mL seed medium according to the inoculum size of 10%, and incubated at 30°C The primary seed liquid was obtained by statically culturing in a constant temperature incubator for 3 days.
[0032] Fermented seed culture: the primary seed liquid is inoculated in the fermented seed culture medium by 10% inoculum size (glucose 80g / L, coconut milk 20g / L, glacial acetic acid 13g / L, soybean peptone 0.01g / L, magnesium sulfate heptahydrate 0.2g / L, pH2.5), cultured statically in a 30°C incubator for 3 days.
[0033] Shallow pan static fermentation: the fermented seed liquid is received in the fermentation medium according to the ...
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