Process for preparation optical pure (R)-2- octanol by microorganism and its special microorganism
A microbial method and optical technology, applied in the field of biological separation of racemic compounds
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Embodiment 1
[0059] Cultivation of bacterial strains: the composition of the medium is that the components contained in each 100ml of culture solution are in g: glucose 2-6, yeast extract 0.25-1, (NH 4 ) 2 HPO 4 0.5~2.0, KH 2 PO 4 0.1~0.5, MgSO 4 ·7H 2 O 0.02~0.06, NaCl 0.0025~0.01, ZnSO 4 ·7H 2 O 0.001~0.005, FeSO 4 ·7H 2 O 0.001~0.005, CuSO 4 ·5H 2 O 0.0001~0.0005, MnSO 4 4H 2 O 0.00025~0.001.
[0060] The culture conditions are as follows: the initial pH is 6.0-8.0, the filling volume is 30%, the culture temperature is 25° C., the rotation speed of the shaking flask is 100-300 rpm, and the culture time is 72 hours.
Embodiment 2
[0062] Cultivation of the bacterial strain: the composition of the culture medium is the same as in Example 1. The culture conditions are as follows: the initial pH is 6.0-8.0, the filling volume is 5%, the culture temperature is 35° C., the rotation speed of the shaking flask is 100-300 rpm, and the culture time is 24 hours.
Embodiment 3
[0064] Preparation of whole cells: Take a loop of C.cylindracea CCTCC M204041 from the slope and inoculate it in a 250ml shaker flask with 30% culture solution at 25°C and 100-300rpm for 72 hours; The body was centrifuged and washed twice with saline, and the whole cells of the strain were collected for transformation reaction.
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