Method for producing long-chain dicarboxylic acid by regulating and controlling fermentation process through redox potential
A long-chain dibasic acid and potential regulation technology, applied in the field of fermentation engineering, can solve the problems of large oxygen demand, large oxygen demand and large heat release
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Embodiment 1
[0047] In the present embodiment, the production of long-chain dibasic acid is carried out by the following method, which specifically includes the following steps:
[0048] (1) Strain activation: take a piece of Candidaviswanathii (Candidaviswanathii) and spread it on a large test tube of 20×180mm on a solid slant medium, and cultivate it at 27°C for 72h. The slant medium is malt with pH=6.4 juice agar medium;
[0049] (2) Seed culture: inoculate the activated bacterial classification on the seed culture medium (100mL) in the 500ml Erlenmeyer flask, at 27 ℃, shake culture 40h under 200r / min, the seed culture medium used in the described seed culture process The composition is glucose 20g / L, disodium hydrogen phosphate 2g / L, yeast extract 1g / L, corn steep liquor 2g / L, urea 0.5g / L, n-dodecane 100mL / L, and the pH of the seed medium is 6.0;
[0050] (3) acid production by fermentation: the seed culture obtained in step (2) was inoculated into a 7.5L fermenter with 3L fermentatio...
Embodiment 2
[0054] The only difference between this example and Example 1 is that the fermentation acid production process is: the seed culture obtained in step (2) is inoculated into a 7.5L fermenter with 3L fermentation medium at an inoculum size of 10% (parallel Carry out three experiments), control the initial pH 4.0, control the fermentation temperature at 27°C, the ventilation rate of sterile air is 0.1vvm, the stirring speed is 50rpm, when the ORP is lower than 0mV, gradually increase the stirring speed (maximum no more than 1000rpm) , Ventilation (maximum not exceeding 4.0vvm) and adding reducing agent or oxidizing agent, control the ORP near 0mV, adjust the pH to 7.0, 8.0 and 9.0 when the glucose is consumed, and control the ORP near 50mV, at the same time through continuous or intermittent Add n-dodecane in a way so that the concentration of n-dodecane in the fermentation broth is always greater than or equal to 1% (v / v), cultivate for 114 hours, and the acid production is 40.6g / ...
Embodiment 3
[0058] The only difference between this example and Example 1 is that the fermentation acid production process is: the seed culture obtained in step (2) is inoculated into a 7.5L fermenter with 3L fermentation medium at an inoculum size of 10% (parallel Carry out three experiments), control the initial pH 4.0, control the fermentation temperature at 27°C, the ventilation rate of sterile air is 0.1vvm, the stirring speed is 50rpm, when the ORP is lower than 0mV, gradually increase the stirring speed (maximum no more than 1000rpm) , ventilation (maximum not exceeding 4.0vvm) and adding reducing agent or oxidizing agent, control the ORP around 0mV, adjust the pH to 7.0, 8.0 and 9.0 when the glucose is consumed, and control the ORP around 100mV, and at the same time through continuous or intermittent Add n-dodecane in a way so that the concentration of n-dodecane in the fermentation broth is always greater than or equal to 1% (v / v), cultivate for 114 hours, and the acid production ...
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