Technology for producing acetaldehyde in one step in microbial fermentation method
A microbial fermentation method, acetaldehyde technology, applied in the direction of microorganism-based methods, microorganisms, biochemical equipment and methods, etc., can solve the problem of high cost of acetaldehyde, and achieve the effect of reducing production costs
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Embodiment 1
[0028] Scrape the slanted seeds and inoculate them into 250mL Erlenmeyer flasks filled with liquid medium, each containing 50mL of medium. Seed medium (g / 100mL) consists of glucose: 4, yeast extract: 0.5, potassium dihydrogen phosphate: 0.1, ammonium sulfate: 0.1, magnesium sulfate: 0.05, agar: 2 (for solid medium, liquid seed medium Not added), pH: 7. After the medium is prepared, it is sterilized at 121°C for 20 minutes, cooled and then inoculated. Place the inoculated Erlenmeyer flask on a constant temperature shaker at 25° C., and vibrate at 220 rpm for 48 hours to obtain liquid seeds.
Embodiment 2
[0030] Configure a high-density fermentation medium (g / L), and its composition is as follows: glucose: 150, yeast extract: 10, peptone: 10, ammonium sulfate: 1, potassium dihydrogen phosphate: 1, magnesium sulfate: 1, pH: 7.
[0031] In a 15L full-automatic fermenter, add the above culture medium according to the filling volume of 70% (v / v), and cool to about 25° C. after steam sterilization. Insert the cultured liquid seeds according to the inoculum amount of 5%, carry out aerobic cultivation at a temperature of 25° C. and a stirring speed of 150 rpm, so that the dissolved oxygen level of the fermentation liquid in the tank fluctuates between 30% and 35%. The residual sugar content was detected every 6 hours. When the residual sugar concentration was lower than 5g / L, feed was carried out. After 2 feeds, the wet weight of the cells reached 14.3g / L. At this time, the tank was selected.
Embodiment 3
[0033] Evenly disperse the wet cells obtained by centrifugation in PBS buffer solution with a concentration of 0.2mol / L and a pH of 7.5 to make a 20g / L bacterial suspension, and add hydrogen peroxide at a volume ratio of 1:6 at 25°C Immediately after 10 minutes of solution treatment, the hydrogen peroxide-containing mixture was inoculated.
[0034]In a 100L fermenter, add a 60% (v / v) liquid volume to the fermentation medium, and its composition (g / L) is: glucose: 100, yeast extract: 10, ammonium sulfate: 1, potassium dihydrogen phosphate : 1, magnesium sulfate: 0.5, pH: 7, steam sterilized and cooled to 30°C. Pasteurized n-dodecane was added in a ratio of 2% (v / v), the stirring speed was 150 rpm, and the mixture was thoroughly mixed for 15 minutes. Insert the above-mentioned cell fluid treated with hydrogen peroxide at an inoculum amount of 5% (v / v), control the temperature at 30°C, and ventilate at 0.2v / v.min. The stirring speed is automatically controlled within 500rpm, and...
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