Process of regenerating internal cell coenzyme NADP11 by pentose and its application
A coenzyme regeneration, pentose sugar technology, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc.
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Embodiment 1
[0047] Resuspend 2 g of Candida parapsilosis wet cells that have catalyzed a transformation reaction in 20 ml of 100 mmol / L potassium phosphate buffer solution (pH6.5), add 300 mg of racemic phenylethylene glycol, 40 mg of xylose , Reacted at 30°C, 150r / min for 48h. After the reaction, the mixture was centrifuged, and the supernatant was taken for extraction. The optical purity of the product (S)-PED was 91.53% e.e., and the yield was 80.41%.
Embodiment 2
[0049] Resuspend 2 g of Candida parapsilosis wet cells that have catalyzed a conversion reaction in 20 ml of 100 mmol / L potassium phosphate buffer solution (pH6.5), add 300 mg of racemic phenylethylene glycol, 400 mg of xylose , Reacted at 30°C, 150r / min for 48h. After the reaction, the mixture was centrifuged, and the supernatant was taken for extraction. The optical purity of the product (S)-PED was 93.12% e.e., and the yield was 82.19%.
Embodiment 3
[0051] Resuspend 2 g of Candida parapsilosis wet cells that have catalyzed a conversion reaction in 20 ml of 100 mmol / L potassium phosphate buffer solution (pH6.5), add 300 mg of racemic phenyl glycol, 160 mg of xylose , Reacted at 30°C, 150r / min for 48h. After the reaction, the mixture was centrifuged, and the supernatant was taken for extraction. The optical purity of the product (S)-PED was 98.72% e.e., and the yield was 86.43%.
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