Method using streptomyces lavendulae fermentation to produce alpha-glucosidase inhibitors
The technology of Streptomyces lilacinus and glucosidase is applied in the field of microbial fermentation to achieve the effects of improving the formation of hyperglycemia, convenient operation and implementation, and high production efficiency
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Embodiment 1~8
[0036] (1) Activation and preservation of strains
[0037] Streptomyces lilacinus ( Streptomyces lavendulae ) UN-8 was inoculated on a solid slant medium, cultured at a constant temperature of 30°C for 3 days, and stored at 4°C for a short period of time. The concentration components of the solid slant medium prepared with distilled water are: soluble starch 20g / L, KNO 3 0.5g / L, NaCl0.5g / L, K 2 HPO 4 1.0g / L, MgSO 4 ·7H 2 O0.5g / L, FeSO 4 ·7H 2 O0.01g / L, agar 20g / L, pH value 7.2.
[0038] (2) Preparation of seed solution
[0039] Primary seed preparation: put 2.0cm on the above slope 2 The bacterial lawn was inserted into a 500mL Erlenmeyer flask containing 100mL of liquid seed medium, the shaking table was rotated at 160rpm, and cultured at a constant temperature of 30°C for 36h; secondary seed preparation: the primary seed liquid was inserted into 600mL of liquid seed medium In a 3.0L Erlenmeyer flask, the inoculum amount was 2% (v / v), the shaker rotated at 160rpm, ...
Embodiment 9~16
[0045] (1) Activation and preservation of strains
[0046] Streptomyces lilacinus ( Streptomyces lavendulae ) UN-8 was inoculated on a solid slant medium, cultured at a constant temperature of 30°C for 3 days, and stored at 4°C for a short period of time. The concentration components of the solid slant medium prepared with distilled water are: soluble starch 20g / L, KNO 3 0.5g / L, NaCl0.5g / L, K 2 HPO 4 1.0g / L, MgSO 4 ·7H 2 O0.5g / L, FeSO 4 ·7H 2 O0.01g / L, agar 20g / L, pH value 7.2.
[0047] (2) Preparation of seed solution
[0048] Primary seed preparation: put 2.0cm on the above slope 2 The bacterial lawn was inserted into a 500mL Erlenmeyer flask containing 100mL of liquid seed medium, the shaking table was rotated at 160rpm, and cultured at a constant temperature of 30°C for 36h; secondary seed preparation: the primary seed liquid was inserted into 600mL of liquid seed medium In a 3.0L Erlenmeyer flask, the inoculum amount was 2% (v / v), the shaker rotated at 160rpm, ...
Embodiment 17
[0054] (1) Activation and preservation of strains
[0055] Streptomyces lilacinus ( Streptomyces lavendulae ) UN-8 was inoculated on a solid slant medium, cultured at a constant temperature of 28°C for 5 days, and stored at 4°C for a short period of time. The concentration components of the solid slant medium prepared with distilled water are: soluble starch 10g / L, KNO 3 0.2g / L, NaCl0.2g / L, K 2 HPO 4 0.5g / L, MgSO 4 ·7H 2 O0.2g / L, FeSO 4 ·7H 2O0.005g / L, agar 20g / L, pH value 7.0.
[0056] (2) Preparation of seed solution
[0057] Primary seed preparation: put 1.0cm on the above slope 2 The bacterial lawn was inserted into a 500mL Erlenmeyer flask containing 100mL of liquid seed medium, the shaking table was rotated at 200rpm, and cultured at a constant temperature of 28°C for 48h; secondary seed preparation: the primary seed liquid was inserted into 600mL of liquid seed medium In a 3.0L Erlenmeyer flask, the inoculum size was 5% (v / v), the shaker was rotated at 200 rp...
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