Methylotrophic bacillus and application thereof
A methylotrophic, bacillus-based technology applied to bacteria, microbe-based methods, microorganisms, etc.
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Embodiment 1
[0019] Embodiment 1: the screening of bacterial strain
[0020] Grind medium-high temperature Daqu (taken from Anhui Shuanglun Employment Co., Ltd.) into powder, accurately weigh 25 g and add it to a conical flask containing 200 ml of sterile normal saline. Add sterilized glass beads and put them on a shaker (180r / min) at room temperature for 30 minutes to disperse, then take them out and let them stand for 30 minutes. Take 1 mL of supernatant and add 9 mL of sterile saline to prepare a volume concentration of 10 - 1 bacterial suspension. By analogy, the volume concentration is prepared to be 10 - 3 、10 - 4 ...10 -7 bacterium suspension, evenly spread on the separation medium that has been cooled overnight (the preparation method of the separation medium is: beef extract 3g / L, peptone 10g / L, NaCl 5g / L, agar strip 20 g / L, water 1000mL, mixed with nystatin 0.01g / L, adjust the pH to 7.0, sterilize at 121°C for 20min.) on the plate, place the inoculated plate in a cons...
Embodiment 2
[0021] Example 2: Fermentation of bacterial strains
[0022] 1. Fermentation of strains
[0023] Pick bacterial strains from the slope to the seed medium (the preparation method of the seed medium is: beef extract 20.0 g, glucose 20.0 g, K 2 HPO 4 1.0 g, (NH 4 ) 2 SO 4 1.0 g, MgSO 4 ·7H 2 O 1.0 g, NaCl 0.5 g, FeSO 4 ·7H 2 O 0.01 g, mix well, add distilled water to adjust to 1L, adjust pH to 7.0, sterilize at 121°C for 20min. ) to the logarithmic phase, and the strains cultivated to the logarithmic phase with the seed medium were added to the fermentation medium at a 5% inoculum (the preparation method of the fermentation medium was: 20.0 g of beef extract, 20.0 g of glucose, K 2 HPO 4 1.0 g, (NH 4 ) 2 SO 4 1.0 g, MgSO 4 ·7H 2 O 1.0 g, NaCl 0.5 g, FeSO 4 ·7H 2 O 0.01 g, mix well, add distilled water to adjust to 1L, adjust pH to 7.0, sterilize at 121°C for 20min. ), and then cultured with shaking at 37°C and 150r / min for 72h. The fermentation broth was c...
Embodiment 3
[0026] Embodiment 3: the detection of acetoin
[0027] Gas chromatographic detection conditions: the fermentation broths of the different strains obtained in Example 2 were diluted 5 times respectively, and then 2 μL samples were taken for gas chromatographic analysis to detect the output of acetoin. After testing, the highest yield of acetoin was 15.71g / L.
[0028] Gas chromatographic parameters: CP-Wax 57 C column for liquor, inner diameter: 250.00 μm, length: 50.0 m, liquid film thickness: 0.20 μm, dead time: 2.983 min, column temperature: 60°C for 5 minutes, 5°C / min program Heat up to 140°C and keep for 2min, inlet temperature: 150°C, detector temperature: 160°C, carrier gas: N2, column pre-pressure 90kPa, makeup: 30mL / min, split ratio: 1:30, air: 50kPa, Hydrogen: 50kPa.
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