Method for extracting xylitol and D-galactitol from xylose mother solution
A technology for preservation of xylose and strains, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problems of reducing corporate profits, high viscosity, complex components, etc.
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Embodiment 1
[0011] Inoculate the engineered strain BSxyl into 10ml LB and cultivate overnight to be the primary seed, transfer 5ml of the primary seed to 50ml fermentation medium (12% xylose mother liquor, 1.0% yeast powder, 0.5% peptone, pH6.5) and culture at 200rpm Obtain secondary seeds overnight, inoculate all 50 ml of secondary seeds into 450 ml of the same fermentation medium, culture at 200 rpm for 48 hours, and take samples to detect the content and purity of xylose. Calculated by combining xylose and D-galactose, after 48 hours of purification, the metabolism of L-arabinose and glucose is incomplete, and the total purity of xylose and galactose in the fermentation broth reaches 70.6%.
Embodiment 2
[0013] Inoculate the engineered strain BSxyl into 10ml LB and cultivate overnight to be the primary seed, transfer 5ml of the primary seed to 50ml fermentation medium (12% xylose mother liquor, 1.0% yeast powder, 0.5% peptone, pH6.5) and culture at 200rpm Obtain secondary seeds overnight, inoculate all 50 ml of secondary seeds into 450 ml of the same fermentation medium, culture at 200 rpm for 60 hours, and take samples to detect the content and purity of xylose. Calculated by combining xylose and D-galactose, after 60 hours of purification, both L-arabinose and glucose are completely metabolized, and the total purity of xylose and galactose in the fermentation broth reaches 88.8%.
Embodiment 3
[0015] Inoculate the engineered strain BSxyl into 10ml LB and cultivate overnight to be the primary seed, transfer 5ml of the primary seed to 50ml fermentation medium (12% xylose mother liquor, 1.0% yeast powder, 0.5% peptone, pH6.5) and culture at 200rpm Obtain secondary seeds overnight, inoculate all 50 ml of secondary seeds into 450 ml of the same fermentation medium, culture at 200 rpm for 72 hours, and take samples to detect the content and purity of xylose. Calculated by combining xylose and D-galactose, after 72 hours of purification, both L-arabinose and glucose were completely metabolized, and the total purity of xylose and galactose in the fermentation broth reached 89.2%.
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