Method for preparing deep-sea bacterial polysaccharides in low cost
A deep-sea bacteria, low-cost technology, applied in microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problems of high fermentation cost, affecting the development and application of polysaccharides, etc., to achieve lower fermentation costs, good environmental benefits and social benefits. Benefit, the effect of reducing fermentation cost
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Embodiment 1
[0038] A preparation method of deep-sea bacterial polysaccharide, the steps are as follows:
[0039] (1) The deep-sea bacteria (Zunongwangia profunda) SM-A87 strain was inoculated in the liquid seed medium, and shaken at 20°C for 3 days to obtain the seed culture solution;
[0040] The components of the liquid seed culture medium are as follows, all in parts by weight:
[0041] 0.8 parts of peptone, 0.75 parts of yeast powder, 100 parts of artificial seawater, pH 8.0;
[0042] (2) Inoculate the seed culture solution prepared in step (1) on the fermentation medium at a volume percentage of 5%, and culture it for 20 hours at 20°C and the dissolved oxygen saturation is higher than 30%, and then adjust the fermentation temperature to Continue culturing at 12°C for 8 days, and add whey concentrate during the period of continuing culturing to obtain a fermented liquid;
[0043] The components of the fermentation medium are as follows, whey is parts by volume, and the unit is in mi...
Embodiment 2
[0056] A preparation method of deep-sea bacterial polysaccharide, the steps are as follows:
[0057] (1) The deep-sea bacteria (Zunongwangia profunda) SM-A87 strain was inoculated in the liquid seed medium, and shaken at 15°C for 3 days to obtain the seed culture solution;
[0058] The components of the liquid seed culture medium are as follows, all in parts by weight:
[0059] 1.0 parts of peptone, 0.5 parts of yeast powder, 100 parts of artificial seawater, pH 7.5;
[0060] (2) Inoculate the seed culture solution prepared in step (1) on the fermentation medium at a volume percentage of 3%, and culture it for 30 hours at 15°C and the dissolved oxygen saturation is higher than 30%, and then adjust the fermentation temperature to Continue culturing at 8°C for 10 days, and add whey concentrate during the period of continuing culturing to obtain a fermented liquid;
[0061] The components of the fermentation medium are as follows, whey is parts by volume, and the unit is in mil...
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