Preparation method of biological pigment by double-strain fermentation with wastewater rich in amino acids as base material
A biopigment and amino acid technology, applied in the direction of microorganism-based methods, biochemical equipment and methods, fermentation, etc., can solve the problems of low yield and high fermentation cost, and achieve high yield, high-efficiency expression intensity, and strong ecological acceptability.
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Embodiment 1
[0032] (1) Preparation of seed medium
[0033] Neurospora crassa (Neurospora crassa ATCC10815) and black fungus (Auricularia auricula) were inoculated on PDA plates from the slant preservation tubes and cultured at 28°C for 10 days, and the colony morphology was shown in the figure ( figure 1 ). During the 10-day cultivation process, the seed medium was prepared;
[0034] Seed medium: 200 ml of milk factory waste water (after filtering to remove impurities, the total content of main components amino acid and protein 0.6%, oil 0.02%), add glucose 6g, peptone 4g, CaCl 2 0.07g, vitamin B 0.1g, vitamin C 0.1g, adjust pH 7.0-8.0. The culture medium was sterilized at 115°C for 30 min under high temperature and high pressure.
[0035] (2) Preparation of primary seed solution
[0036] On the PDA plate, 8 pieces of 0.5mm × 0.5mm bacterium blocks were picked, respectively inoculated in the seed culture medium of 200mL, and 26 ℃, 150rpm shake flask cultured for 3 days, as the first-...
Embodiment 2
[0046] (1) Preparation of seed medium
[0047] Neurospora crassa (Neurospora crassa ATCC10815) and black fungus (Auricularia auricula) were inoculated on PDA plates from slant preservation tubes and cultured at 28°C for 10 days. During the 10-day cultivation process, the seed medium was prepared;
[0048] Seed medium: 2000 ml of waste water rich in amino acids, milk factory waste water (after filtering to remove impurities, the total content of amino acids and protein in the main components is 0.6%, and oil 0.02%), add glucose 60g, peptone 30g, CaCl 2 0.6g, vitamin B 0.5g, vitamin C 0.5g, adjust the pH to 7.0-8.0. The medium was sterilized at 115°C for 30 min under high temperature and high pressure.
[0049] (2) Preparation of primary seed solution
[0050] Pick 20 pieces of 0.5mm×0.5mm bacterial pieces on the PDA plate, inoculate them in 2000mL seed culture medium respectively, and cultivate them at 26°C and 150rpm for 4 days as the primary seed solution.
[0051] (3) P...
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