Preparation method of laver extract and application of laver extract in aquaculture
A technology of extract and seaweed, applied in the field of preparation of seaweed extract, to achieve the effects of reducing usage, facilitating large-scale preparation, and improving immunity and survival rate
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Embodiment 1
[0023] Take 100g of crushed seaweed, add 30 times of water, add 1.5g cellulase, 1g pectinase, adjust pH to 5.5, 50°C, react for 2h, add 1.5g trypsin, adjust pH to 8.0, 37°C, 1h; then add 1.5 g alkaline protease, pH 8.0, 50°C, 3h; heat to 95°C to inactivate the enzyme for 15min, centrifuge at 6000rpm for 30min, concentrate the retentate under reduced pressure at 50°C, desalt by nanofiltration, and freeze-dry to obtain laver extract P1.
Embodiment 2
[0024] Embodiment 2, the preparation (P2) of laver extract
[0025] Take 100g of crushed laver, add 40 times of water, add 3.0g cellulase, 3.0g pectinase, adjust pH to 5.0, 55°C, react for 3h, add 3.0g trypsin, adjust pH to 9.0, 40°C, 3h; then Add 3.0 g of alkaline protease, pH 9.0, 55°C, 4h; heat to 90°C to inactivate the enzyme for 20 minutes, centrifuge at 7000rpm for 20 minutes, concentrate the retentate under reduced pressure at 55°C, desalt by nanofiltration, and freeze-dry to obtain laver extract P2.
Embodiment 3
[0026] Embodiment 3, the preparation (P3) of laver extract
[0027] Take 100g of crushed seaweed, add 20 times of water, add 1.0g cellulase, 1.0g pectinase, adjust pH to 5.5, 50°C, react for 2h, add 1.0g trypsin, adjust pH to 9.0, 35°C, 2h; then add 1.5g alkaline protease, pH 7.8, 45°C, 2h; heat to 100°C to inactivate the enzyme for 10min, centrifuge at 7500rpm for 30min, concentrate the retentate under reduced pressure at 50°C, desalt by nanofiltration, and freeze-dry to obtain laver extract P3.
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