A kind of amphoteric glycolipid biosurfactant and preparation method thereof
A biosurface and amphoteric glycolipid technology, applied in biochemical equipment and methods, methods based on microorganisms, microorganisms, etc., can solve the problem of overall effect decline, achieve low cost, scientific, reasonable and effective synthesis methods, and good compatibility Effect
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Embodiment 1
[0057] The preparation method of amphoteric glycolipid biosurfactant molecule is
[0058] 1. Bacteria: Amphoteric glycolipid biosurfactants need to be cultivated in sequence with three bacteria, Pseudomonas aeruginosa (ATCC 15442), Candida albicans (ATCC 10231), and Neurospora crassa (ATCC 18889).
[0059] 2. Medium: NaNO 3 : 0.4%, FeCl 2 : 0.002%, NaH 2 PO 4 : 0.25%, K 2 HPO 4 : 0.25%, MgSO 4 ·7H 2 O: 0.005%, KCl: 0.05%, Choline chloride: 0.05%, fatty amine: 0.5%, corn syrup: 0.05%, soybean oil 5%: 3.0%, glucose: 0.1%, yeast extract powder: 0.001%, initial pH 6 -7.
[0060] 3. Seed shake flask culture
[0061] The slant strains were cultured for 48 hours, and the three above-mentioned single-bacteria slants were respectively transferred to 1L Erlenmeyer flasks, in which 200mL of LB or YPD medium was filled in the Erlenmeyer flasks, and Pseudomonas and Candida were cultured at about 35°C. Candida was cultured at about 25°C, and Neurospora was cultured at about 30°C f...
Embodiment 2
[0085] Preparation method of amphoteric glycolipid biosurfactant molecule
[0086] 1. Bacteria: Amphoteric glycolipid biosurfactants need to be cultivated in sequence with three bacteria, Pseudomonas aeruginosa (ATCC 15442), Candida albicans (ATCC 10231), and Neurospora crassa (ATCC 18889).
[0087] 2. Medium: NaNO 3 : 1.4%, FeCl 2 : 0.005%, NaH 2 PO 4: 0.4%, K 2 HPO 4 : 0.4%, MgSO 4 ·7H 2 O: 0.01%, KCl: 0.09%, Choline chloride: 0.05%, fatty amine: 0.5%, corn syrup: 0.1%, soybean oil: 4.0%, glucose: 0.3%; yeast infusion powder: 0.004%, initial pH 6-7 .
[0088] 3. Seed shake flask culture
[0089] The slant strains were cultured for 36h-48h, and the three above-mentioned single-bacteria slants were transferred to 1L conical flasks respectively. The conical flasks were filled with 200mL of LB or YPD medium, and Pseudomonas was cultured at about 35°C. Candida candida was cultured at about 25°C, and Neurospora was cultured at about 30°C for 30 hours.
[0090] 4. Produc...
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