Aspergillus ZJUBE 2010 and application thereof
A technology of ZJUBE2010 and marine Aspergillus niger, which is applied to marine Aspergillus niger ZJUBE2010 and its application fields, can solve the problems of high production cost, high manufacturing cost of fermentation equipment, and large energy consumption, so as to reduce equipment manufacturing cost, reduce energy consumption, High conversion effect
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Embodiment 1
[0026] (1) Preparation of spore culture:
[0027] Spore culture medium: adopt potato dextrose agar medium PDA (200 grams of potatoes, 20 grams of glucose, 20 grams of agar powder, and add distilled water to 1 liter), divide the medium into test tubes in 5 milliliters, and sterilize at 121 ° C. After 20 minutes of sterilizing, spread the test tube on a slope until it cools and solidifies.
[0028] The marine Aspergillus niger ZJUBE 2010 was inoculated on the spore medium with an inoculation loop, and cultured at 30°C for 5 days.
[0029] The marine Aspergillus niger ZJUBE 2010 spores were rinsed with 50ml of sterile distilled water and transferred to a 150ml Erlenmeyer flask filled with glass beads, and shaken on a shaker at 180-200rpm for 1 hour to disperse the spores evenly.
[0030] (2) Preparation of seeds
[0031] Seed medium: 1% glucose, 0.25% yeast extract, 0.25% peptone, 1% available carbon source and 0.25% organic nitrogen source, natural pH.
[0032] Inoculation: A...
Embodiment 2
[0041] (1) Preparation of spore culture:
[0042] Spore culture medium: adopt potato dextrose agar medium PDA (200 grams of potatoes, 20 grams of glucose, 20 grams of agar powder, and add distilled water to 1 liter), divide the medium into test tubes in 5 milliliters, and sterilize at 121 ° C. After 20 minutes of sterilizing, spread the test tube on a slope until it cools and solidifies.
[0043] The marine Aspergillus niger ZJUBE 2010 was inoculated on the spore medium with an inoculation loop, and cultured at 35°C for 3 days.
[0044] The marine Aspergillus niger ZJUBE 2010 spores were rinsed with 50ml of sterile distilled water and transferred to a 150ml Erlenmeyer flask filled with glass beads, and shaken on a shaker at 180-200rpm for 1 hour to disperse the spores evenly.
[0045] (2) Preparation of seeds
[0046] Seed medium: 1% glucose, 0.25% yeast extract, 0.25% peptone, 5% available carbon source and 3% organic nitrogen source, natural pH.
[0047] Inoculation: Adju...
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