Aspergillus Niger Producing Hydrolase and Its Application in Preparation of Lentinus edodes Enzymolyzate
A technology for enzymatic hydrolysate of Lentinus edodes and Aspergillus niger, applied in the directions of hydrolase, application, food preparation, etc., can solve the problems of difficult practical application and high cost, achieve high nutritional value and health care efficacy, low production cost and delicious taste. Effect
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Embodiment 1
[0024] Example 1: Enrichment, isolation, screening and mutation breeding of enzyme-producing microorganisms
[0025] Commercially available fresh shiitake mushrooms were chopped, weighed 25g into a 250mL Erlenmeyer flask, added 5g of freshly collected vegetable field soil, stirred evenly with a small amount of water, placed in an incubator at 30°C for 5 days to enrich enzyme-producing microorganisms.
[0026] Dilute the above-mentioned enrichment material covered with mold with sterile water, spread it on the plate medium, and cultivate it in a biochemical incubator at 30° C. for 3 days until a large number of colonies are formed. Pick the spores of mold colonies with different colors and shapes and inoculate them on the slant medium. The slant culture is based on constant temperature cultivation at 30°C for 3 days to obtain spore-filled slant strains.
[0027] Use an inoculation loop to pick the spores of the slant strains of the above strains, put them into 50mL enzyme-produ...
Embodiment 2
[0033] Embodiment 2: be used to prepare the hydrolase fermentation of shiitake mushroom hydrolyzate
[0034] Using Aspergillus niger MJ as the enzyme-producing strain, after optimizing the medium composition and fermentation conditions, the prepared crude enzyme solution hydrolyzed Lentinus edodes, and the comprehensive content of amino acids, 5′-nucleotides and polysaccharides in the hydrolyzate increased to a certain extent. The hydrolysis rate of shiitake mushrooms reaches 36.8%, which is 43.2% higher than that before optimization. The preferred preparation method is as follows:
[0035] (1) The Aspergillus niger MJ strain preserved on the slant of the test tube was inoculated on the slant medium, and the slant was cultured in a biochemical incubator at 30°C for 2 days. The slant medium is prepared according to the following composition and method: wash and peel the potatoes, cut them into small pieces, weigh 200g, add 1000mL of tap water and boil for 30min, filter the potato...
Embodiment 3
[0040] Embodiment 3: the preparation of mushroom hydrolyzate
[0041] Remove the stalks of commercially available fresh shiitake mushrooms, wash them, dry them in an oven at 85°C for 24 hours, and grind them fully with a pulverizer. Put 50 mL of the enzyme solution prepared in Example 2 into a 250 mL Erlenmeyer flask, add 10 g of shiitake mushroom powder, seal the Erlenmeyer flask with plastic wrap, and biotransform in a water bath shaking box at 30°C and 200 r / min for 12 hours. The enzymatic solution was filtered with 4 layers of gauze to remove unenzymolyzed residues, the filtrate was concentrated under reduced pressure, dried in a vacuum and then pulverized to obtain 3.68 g of enzymatic hydrolyzate of shiitake mushrooms, with a calculated hydrolysis yield of 36.8%.
[0042] Use the ninhydrin colorimetric method to measure the amino nitrogen content of the shiitake mushroom enzymolyzate prepared by the above method, determine the 5'-nucleotide content by the periodic acid ox...
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