A strain of Durianella and its application
A technology of Duganella and blue pigment, applied in the direction of bacteria, microorganisms, microorganisms, etc., can solve the problems of reducing the competitiveness of microbial blue pigment, restricting the development of microbial blue pigment, unfavorable large-scale production of pigment, etc., to facilitate industrial production, Short cycle, less demanding effect
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Embodiment 1
[0020] Example 1 Isolation and identification of Dujania T2013CCTCC M2014643
[0021] 1. Sample collection
[0022] The soil samples were collected from slope soil samples in Zigong City, Sichuan Province.
[0023] 2. Isolation and screening of strains
[0024] Medium preparation:
[0025] (1) Beef extract peptone medium:
[0026] 10g peptone, 3g beef extract, 5g sodium chloride, 15-20g agar, add distilled water to make 1000mL solution, adjust the pH to 7.0-7.2, sterilize with moist heat at 121°C for 20min.
[0027] (2) Potato medium (PDA medium):
[0028] Commercially available potato (peeled) 200g, glucose 20g, agar 15-25g, distilled water 1000mL; pH natural, 121°C moist heat sterilization for 20min.
[0029] (3) Gao's medium I:
[0030] Soluble starch 20g / L, KNO 3 1.0g / L, NaCl 0.5g / L, K 2 HPO 4 ·3H 2 O 0.5g / L, MgSO 4 ·7H 2 O0.5g / L, FeSO 4 ·7H 2 O 0.01g / L; pH 7.2~7.4, sterilized by moist heat at 121℃ for 20min.
[0031] Separation of strains: Take 10g of soil sample and put it in a 250mL E...
Embodiment 2
[0037] Example 2 Preparation of blue pigment with Dujuni T2013CCTCC M2014643
[0038] Strain activation: first put the strains preserved in the frozen glycerol tube into warm water at 50℃ for 30 minutes, then inoculate the thawed strains into the Gao's No. I medium, activate for 24 hours, and then carry out coating treatment and streaking separation. Repeat the plate streak separation operation until the microscopic examination is a pure strain (the cell morphology is consistent).
[0039] Preparation of seed solution: Pick a single colony from the above-mentioned plate-cultured strains and inoculate it into liquid Gaussian No. I medium for 24 hours at 30°C.
[0040] Shake flask fermentation: optimized medium (soluble starch 15g, KNO 3 1.2g, NaCl 0.6g, K 2 HPO 4 ·3H 2 O0.4g, MgSO 4 ·7H 2 O 0.55g, FeSO 4 ·7H 2 O 0.018 g, pH 7.6), 70 mL of culture medium was put into a 250 mL shake flask, the inoculum was 2%, the fermentation temperature was 30° C., the shaker speed was 150 r / min, and...
Embodiment 3
[0050] Example 3 Preparation of blue pigment using Durania T2013CCTCC M2014643
[0051] Strain activation: first put the strains preserved in the frozen glycerol tube into warm water at 50℃ for 30 minutes, then inoculate the thawed strains into the Gao's No. I medium, activate for 24 hours, and then carry out coating treatment and streaking separation. Repeat the plate streak separation operation until the microscopic examination is a pure strain (the cell morphology is consistent).
[0052] Preparation of seed solution: pick a single colony from the above-mentioned plate-cultured strains and inoculate it into liquid Gaussian No. I medium for 24h, 30℃, and shaker rotation speed 180r / min.
[0053] Shake flask fermentation: Optimized medium (soluble starch 15g, KNO3 1.2g, NaCl 0.6g, K2HPO4·3H2O 0.4g, MgSO4·7H2O 0.55g, FeSO4·7H2O 0.018g, pH7.6), fill 70mL of medium Into a 250mL shake flask, the inoculum amount is 5%, the fermentation temperature is 30°C, the shaker rotation speed is 18...
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