Culture medium for fermenting panus rudis to produce laccase and laccase production method
A culture medium formula and culture medium technology, applied in the field of laccase production by fungal culture, can solve the problems of low laccase production, long culture period, and easy pollution, and achieve short laccase production time, short fermentation cycle, and laccase production. The effect of high vitality
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Embodiment 1
[0025] Embodiment 1 single factor experiment determines optimum medium composition
[0026] (1) Preparation of seed medium and basal medium
[0027] (a) Seed medium: based on the weight of 1L medium, it contains 15% potato juice, 1% glucose, 0.2% ammonium tartrate, and the pH is natural. 1.01MPa, high pressure steam sterilization for 20min.
[0028] (b) Basal medium: based on the weight of 1L medium, containing 15% potato juice, 1% glucose, 0.2% ammonium tartrate, and natural pH. 1.01MPa, high pressure steam sterilization for 20min.
[0029] (c) Potato agar medium: PDA basal medium
[0030] (2) Production of fermented seeds: inoculate the Auricularia fungus FG-35 (Panus rudis FG-35, preservation number: CCTCC NO: M2013106) on potato agar medium, culture at 31°C for 5 days, and wait for it to produce spores , that is, activation; inoculate the activated spores of the strain into the seed medium with an inoculation needle, and cultivate for 96 hours at 31°C with a rotation s...
Embodiment 2
[0047] Example 2 Response Surface Determination of Optimal Fermentation Medium
[0048] (1) Experiment to determine the best medium
[0049] On the basis of determining the single-factor experimental medium, determine the best components, change the concentration of each component, and configure different mediums, the method is the same as the steps (1) and (2) in Example 1. See Table 1, inoculate the same amount of inoculum (0.5%) seed solution into a 300mL conical flask filled with 50-90mL medium, and the number of spores of the strains inserted is 2×10 6 -5×10 6 About one, cultivated at 28-32°C for 4-8d at a rotational speed of 160-180r / min. Then measure the enzyme activity according to the steps (3) and (4) of Example 1. Three groups of experiments, 1, 5, and 14 with the best results of Plackett-Burman and the steepest climbing experiment and the highest enzyme production, were selected for verification experiments.
[0050] (2) Plackett-Burman screening factors affect...
Embodiment 3
[0074] Embodiment 3 leather ear fungus produces laccase fermentation method
[0075] (1) Preparation of seeds
[0076] (A) Strain and culture medium
[0077] Strain: Auricularia FG-35
[0078] Slant medium: PDA basal medium
[0079] Ingredients of seed liquid medium: 15% potato juice (1L), 1% glucose, 0.2% ammonium tartrate, natural pH.
[0080] (B) Preparation of seed solution
[0081] Transfer the bacteria on the slope into a 300mL Erlenmeyer flask filled with 50mL of medium, and culture it in a constant temperature shaking incubator at 31°C and 160r / min for 96h, so that the bacterial liquid becomes viscous, indicating that the seeds have grown well up.
[0082] (2) Fermentation culture
[0083] Fermentation medium: the optimal medium optimized according to the response surface: containing soluble starch 10.04g / L, peptone 0.2g / L, K 2 HPO 4 0.50g / L, KH 2 PO 4 0.50g / L, ZnSO 4 ·7H 2 O 0.01g / L, MgSO 4 ·7H 2 O 0.5g / L, CuSO 4 ·7H 2 O 0.01g / L, FeSO 4 ·7H 2 O 0.0...
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