Method for extracting and purifying lignin peroxidase by using reverse micelles
A technology of peroxidase and reverse micelles, which is applied in the field of extraction and purification of enzymes, can solve the problems of inactivation of enzyme protein variability, hinder the progress of reverse micelles extraction and purification of enzymes, reduce the effectiveness of enzyme catalysis, and achieve the degree of purification High, short extraction time and easy operation
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Embodiment 1
[0026] A method for reverse micellar extraction and purification of lignin peroxidase of the present invention, specifically comprising the following steps:
[0027] (1) Preparation of reverse micelle solution: the reverse micelle solution of this example includes biosurfactant, isooctane and n-hexanol, wherein the surfactant is rhamnolipid; After cultivation, it was dissolved in a mixture of isooctane and n-hexanol with a volume ratio of 1:1, and prepared into a 40mL reverse micellar solution with a concentration of 2.75mmol / L (rhamnolipid-n-hexanol-isooctane solution ).
[0028] (2) Pre-extraction process: put 100mL of conventional liquid fermentation medium after autoclaving in a 500mL Erlenmeyer flask, and inoculate 4×10 8 Put the spores of Phanerochaete chrysosporium BKM-F-1767 (not limited to this strain, other Phanerochaete chrysosporium strains are acceptable) into the liquid fermentation medium, and place on a shaking table at a temperature of 37°C and a speed of 150...
Embodiment 2
[0035] A method for reverse micellar extraction and purification of lignin peroxidase of the present invention, specifically comprising the following steps:
[0036] (1) Preparation of reverse micelle solution: the reverse micelle solution of this example includes biosurfactant, isooctane and n-hexanol, wherein the surfactant is rhamnolipid; After cultivation, it was dissolved in a mixture of isooctane and n-hexanol with a volume ratio of 1:1.2, and prepared into a 40mL reverse micellar solution with a concentration of 3.0mmol / L (rhamnolipid-n-hexanol-isooctane solution ).
[0037] (2) Pre-extraction process: put 100mL of conventional liquid fermentation medium after autoclaving in a 500mL Erlenmeyer flask, and inoculate 5×10 8 Put the spores of Phanerochaete chrysosporium BKM-F-1767 (not limited to this strain, other Phanerochaete chrysosporium strains are acceptable) into the liquid fermentation medium, and place on a shaker at 38°C and 180r / min. Cultivate for 8 days, use ...
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