A strain of Aspergillus niger with high yield of pectinase and its application
A technology of Aspergillus niger and pectinase, applied in the field of bioengineering, can solve the problems of late start, low enzyme activity, and restrictions on wide application
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Embodiment 1
[0035] Example 1 Aspergillus niger LD-092 fermentation enzyme production and the extraction method of pectinase produced
[0036] The fermentative enzyme production method of Aspergillus niger LD-092 mainly comprises the following steps:
[0037] Slant culture: Pick a ring of Aspergillus niger LD-092 and inoculate it on a solid slant medium, and culture at a constant temperature of 30°C for 36 hours to obtain first-class seeds;
[0038] Shake flask culture: Take a ring of the first-class seeds and insert them into the seed medium, and cultivate them for 48 hours at a constant temperature of 30°C and a shaker speed of 200r / min to obtain the second-class seed liquid;
[0039] Seed tank cultivation: put the secondary seed solution into the seed tank culture medium at a ratio of 15% (v / v) of the inoculation amount, and cultivate for 45 hours at a constant temperature of 30°C and a rotational speed of 200r / min;
[0040] Fermentation tank culture: The seed liquid in the seed tank i...
Embodiment 2
[0051] Embodiment 2 Aspergillus niger LD-092 fermentation performance verification
[0052] Carry out 50L fermenter verification experiment according to the fermentative enzyme production method of embodiment 1 Aspergillus niger LD-092, fermentation cycle 155h, its 7 batches of fermentative enzyme production situation, the pectinase average enzyme activity in the fermented liquid is 82882U / mL, table 1 shows that the strain not only produces high-yield pectinase, but also has remarkable stability in its fermentation performance and the enzymatic activity of pectinase produced by it.
[0053] Table 1 Enzyme production by fermentation of 7 batches of high pectinase-producing strains
[0054]
Embodiment 3
[0055] Embodiment 3 pectinase activity assay method
[0056] (1) Preparation of enzyme liquid: the fermentation liquid was centrifuged at 6000 r / min for 15 min, and the supernatant was collected to be the crude enzyme liquid.
[0057] (2) Determination method: 3,5-dinitrosalicylic acid method (DNS method) is adopted. Take 0.5ml of appropriately diluted crude enzyme solution in a 25mL colorimetric tube, add 2.0ml of 0.4% pectin solution (pH4.0) as a substrate solution, react in a water bath at 45°C for 30min, add DNS solution and boil for 5min, cool down, and constant volume To 25ml, measure the absorbance at 520nm.
[0058] (3) Definition of enzyme activity: under certain conditions, the amount of enzyme needed to decompose pectin to generate 1 μmol galacturonic acid per minute is an enzyme activity unit (U).
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