Aspergillus niger and cultivation method and application thereof
A cultivation method, the technology of Aspergillus niger, applied in the field of microorganisms, can solve the problems of low conversion rate, low enzyme activity, difficult purification, etc., and achieve the effect of improving quality, reducing difficulty and cost, and reducing production cost
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Embodiment 1
[0032] A strain of Aspergillus niger (Aspergillus niger) BLCY-02 was preserved on July 15, 2014 in the General Microbiology Center of China Committee for the Collection of Microbial Cultures, with the preservation number CGMCC No.9449, address: No. 1, Beichen West Road, Chaoyang District, Beijing 3 Institute of Microbiology, Chinese Academy of Sciences.
[0033] The screening process of the above-mentioned Aspergillus niger (Aspergillus niger) BLCY-02 is as follows:
[0034] (1) Enrichment culture
[0035] Select the soil near the fructooligosaccharide production workshop in Bailong Chuangyuan, Dezhou, Shandong, remove the topsoil with a small shovel, take about 10g of soil at a distance of 5-15cm from the ground, dilute 10 times with sterile water, and add Cha's medium for enrichment Cultivation, Cha's medium composition: sodium nitrate 0.3%; dipotassium hydrogen phosphate 0.1%; magnesium sulfate (MgSO4 7H2O) 0.05%; potassium chloride 0.05%; ferrous sulfate 0.001%; sucrose...
Embodiment 2
[0046] The cultivation method of the Aspergillus niger (Aspergillus niger) BLCY-02 described in embodiment 1, the steps are as follows:
[0047] (1) Aspergillus niger (Aspergillus niger) BLCY-02 was inoculated in PDA medium, and activated and cultured for 30 hours at 30°C to obtain an activated strain;
[0048] (2) Take the activated bacterial strain prepared in step (1), inoculate it in the seed culture medium, and proliferate and cultivate it for 30 hours under the condition of 30° C. to obtain the seed liquid;
[0049] Described seed culture medium component is as follows, is weight percent:
[0050] Sodium nitrate 0.3%; Dipotassium hydrogen phosphate 0.1%; Magnesium sulfate (MgSO 4 ·7H 2 O) 0.05%; yeast extract 1%; sucrose 5%, surplus water, pH is 6.0;
[0051] (3) Take the seed solution prepared in step (2), inoculate it in the fermentation medium at a ratio of 1% by volume, and expand the cultivation for 35 hours at 30° C. to obtain the bacterial cell fermentation sol...
Embodiment 3
[0056] The cultivation method of the Aspergillus niger (Aspergillus niger) BLCY-02 described in embodiment 1, the steps are as follows:
[0057] (1) Aspergillus niger (Aspergillus niger) BLCY-02 was inoculated in PDA medium, and activated and cultured for 20 hours at 38°C to obtain an activated strain;
[0058] (2) Take the activated bacterial strain obtained in step (1), inoculate it in the seed culture medium, and proliferate and cultivate it for 20 hours under the condition of 38° C. to obtain the seed solution;
[0059] Described seed culture medium component is as follows, is weight percent:
[0060] Sodium nitrate 0.3%; Dipotassium hydrogen phosphate 0.1%; Magnesium sulfate (MgSO 4 ·7H 2 O) 0.05%; yeast extract 1%; sucrose 5%, balance water, pH is 4.0;
[0061] (3) Take the seed liquid prepared in step (2), inoculate it in the fermentation medium at a ratio of 10% by volume, and expand the cultivation for 20 hours at 38° C. to obtain the bacterial cell fermentation li...
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