Method of producing nicotinamide by catalysis of rhodococcus
A technology of rhodococcus and nicotinamide, which is applied in the field of rhodococcus to catalyze the synthesis of nicotinamide, can solve the problem of low product concentration, achieve the effect of reducing concentration treatment, high total enzyme activity, and simple separation and purification process
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Embodiment 1
[0021] Example 1 A method for catalyzing the synthesis of nicotinamide by Rhodococcus comprises the following steps:
[0022] (1) Preparation of biocatalyst
[0023] Put 60% seed medium into 1L Erlenmeyer flask A, insert 5% strain after sterilization, and shake and culture at 30°C (120rpm) for 72h. Put 60% of the fermentation medium into the 1L Erlenmeyer flask B, put in 6% of the seed liquid after disinfection for fermentation, the ventilation rate is 0.5; the pressure is 0.05MPa; the stirring speed: 120rpm; Under fermentation 72h carry out centrifugation, collect the sediment after centrifugation, set aside,
[0024] Among them, each liter of seed medium contains the following components (g): glucose 15, yeast extract 2, urea 0.6, K 2 HPO 4 0.15, MgSO 4 0.03, NaCl0.15, ammonium molybdate 0.02, adjust pH =7.5 with 3% HCl,
[0025] Each liter of fermentation medium contains the following components (g): glucose 15, yeast extract 3, urea 0.6, K 2 HPO 4 0.15, MgSO 4 0.03...
Embodiment 2
[0028] In this example, the reaction conditions and parameters were kept consistent with those in Example 1, only the feeding times of the substrate and the biocatalyst were changed, and the influence of the feeding times on the catalytic reaction was investigated. For the rest, in this embodiment, 100 g of 3-cyanopyridine and 10 g of biocatalyst were first added to the reactor. When the concentration is lower than 0.5g / L, it starts to add, and the added amount is consistent with the initial amount, and it is continuously added for 5 times. The concentration of 3-cyanopyridine in the reaction solution was detected 5 hours after the fifth supplementary reaction, and the reaction could be terminated when the substrate concentration was less than 0.02 g / L. The reaction solution was centrifuged at 3000rpm for 20min, and the supernatant was frozen and crystallized at 0°C for 3h. After the crystallization of the product nicotinamide was completed, it was separated by refrigerated ce...
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