Formula and preparation method of culture medium used for Niannianle seed-streptomyces microflavus from cultivation to fermentation
A technology of Streptomyces flavinus and culture medium, applied in the direction of microorganism-based methods, bacteria, biochemical equipment and methods, etc., can solve the problem of poor fermentation yield and effect, low fermentation yield, and easy contamination of miscellaneous bacteria And other issues
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Embodiment 1
[0034] Embodiment 1. The effects of adding special substances: trehalose, potassium dichromate and cycloheximide respectively on the solid medium.
[0035] The specific test steps are:
[0036] (1) Prepare culture medium and sterilize.
[0037] CK (Gaoshi No. 1): Soluble starch 20.0g, KNO 3 1.0g, K 2 HPO 4 0.5g, MgSO 4 ·7H 2 O0.5g, NaCl0.5g, FeSO 4 ·7H 2 O0.01g, agar 20g, distilled water 1000mL, pH7.2-7.4.
[0038] 1#: Cycloheximide 40, 60, 80, 100, 120 mg, respectively added on the basis of CK.
[0039] 2#: Potassium dichromate 30, 50, 70, 90 mg, respectively added on the basis of CK.
[0040] 3#: Trehalose 3.0, 3.5, 4.0, 4.5, 5.0g were added on the basis of CK respectively.
[0041] (2) Use a sterilized puncher with the same aperture and rejuvenated strains with the same age to punch out the bacteria cakes, and inoculate them respectively, with 3 repetitions per culture medium, and 1 bacteria cake per repetition, after culturing for 3-5 days , it was observed that...
Embodiment 2
[0043] Example 2. The effects of adding special substances: trehalose, potassium dichromate and cycloheximide respectively on the liquid medium.
[0044] (2) Prepare culture medium and sterilize.
[0045] CK (Gaoshi No. 1): Soluble starch 20.0g, KNO 3 1.0g, K 2 HPO 4 0.5g, MgSO 4 ·7H 2 O0.5g, NaCl0.5g, FeSO 4 ·7H 2 O0.01g, agar 20g, distilled water 1000mL, pH7.2-7.4.
[0046] 1#: Cycloheximide 40, 60, 80, 100, 120 mg, respectively added on the basis of CK.
[0047] 2#: Potassium dichromate 30, 50, 70, 90 mg, respectively added on the basis of CK.
[0048] 3#: Trehalose 3.0, 3.5, 4.0, 4.5, 5.0g were added on the basis of CK respectively.
[0049] (2) Use a hole puncher with the same aperture and strains with the same bacterial age to punch out bacterial cakes and inoculate them respectively. Each culture medium is repeated 3 times, and each repetition is inoculated with 250ml of 50ml medium and 1 bacterial cake inoculum. , 180r / min on a shaking table, cultured at 30°C...
Embodiment 3
[0051] Embodiment 3. Screening of a fermentation production medium of Streptomyces flavinus.
[0052] (1) Mixing of raw and auxiliary materials:
[0053] CK: 20g bean cake powder, 20g glucose, 3g NaCl, CaCO 3 1g, 1000ml water, pH7.2-7.5.
[0054] Medium 1: 10g bean cake powder, 10g corn starch, 10g cassava flour, 1g fish meal, 3g NaCl, CaCO 3 1g, trehalose 3g, cycloheximide 80mg, potassium dichromate 60mg, water 1000ml, pH7.2-7.5.
[0055] Medium No. 2: bean cake powder 10g, corn flour 10g, glucose 10g, sucrose maltose 4g, trehalose 3g, cycloheximide 80mg, potassium dichromate mg, 60NaCl3g, CaCO 3 1g, 1000ml water, pH7.2-7.5.
[0056] Medium 3: 10g bean cake powder, 10g peanut shell, 10g millet flour, 1g fish meal, 3g NaCl, CaCO 3 1g, trehalose 3g, cycloheximide 80mg, potassium dichromate 60mg, water 1000ml, pH7.2-7.5.
[0057] (2) Autoclaving: Sterilize by passing superheated steam, 1.5 kg / cm2, 121°C, 30min.
[0058] (3) Inoculation: when the temperature of the raw and...
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Abstract
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