Non-immetsed type liquid fermentation process of lingin catabolic enzymes from Phanerochaete chrysosporium
A technology of lignin-degrading enzymes and Phanerochaete, which is applied in the field of applied microorganisms, can solve the problems that are not conducive to the large-scale production of lignin-degrading enzymes, reduce the feasibility of fermentation, increase the activity of proteases, etc., and achieve fermentation conditions that are easy to control , Reduce fermentation cost, easy to harvest
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Embodiment 1
[0009] Prepare a carbon-limited (carbon-to-nitrogen ratio 3.8:1) medium containing 5 g / L of glucose, 4.1 g / L of ammonium tartrate, 2.0 g / L of potassium dihydrogen phosphate, 0.5 g / L of magnesium sulfate, and 0.1 g of calcium chloride / L, vitamin B1 1mg / L, and appropriate amount of trace elements. A 0.5cm polyurethane foam block was used as the immobilized culture carrier. After boiling, washing and drying the carrier, put it into a 250ml Erlenmeyer flask (containing 100ml culture medium). The amount of the carrier was 3.0g / 250ml Erlenmeyer flask. The height of the liquid level was 5 times, and the medium and the carrier were sterilized at 113°C for 30 minutes. Aseptically inoculate Phanerochaete chrysosporium BKM-F-1767 spores grown on 30°C potato dextrose agar plate (200g / L potato juice, 20g / L glucose and 20g / L agar) into the culture medium, inoculum size 1×10 5 Spores / ml. The Erlenmeyer flask was placed on a rotary shaker, and the fermentation was carried out in an air en...
Embodiment 2
[0011] Prepare a nitrogen-limited (carbon-to-nitrogen ratio 152.7:1) medium containing 10 g / L of glucose, 0.2 g / L of ammonium tartrate, 2.0 g / L of potassium dihydrogen phosphate, 0.5 g / L of magnesium sulfate, and 0.1 g of calcium chloride / L, vitamin B1 1mg / L, and appropriate amount of trace elements. A 0.5cm polyurethane foam block was used as the immobilized culture carrier, and the carrier was boiled, washed and dried and then put into a 250ml Erlenmeyer flask (containing 100ml culture medium). The amount of the carrier was 2.2g / 250ml Erlenmeyer flask. The height of the liquid level was 3 times, and the medium and the carrier were sterilized together at 113° C. for 30 minutes. Aseptically inoculate Phanerochaete chrysosporium BKM-F-1767 spores grown on 30°C potato dextrose agar plate (200g / L potato juice, 20g / L glucose and 20g / L agar) into the culture medium, inoculum size 1×10 5 Spores / ml. The Erlenmeyer flask was placed on a rotary shaker, and the fermentation was carr...
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