Ampicillin → (R)-(-)-Methyl mandelate
Reaction equation
[CH3:1]C1(C)S[C@@H]2[C@H](NC([C@H](N)C3C=CC=CC=3)=O)C(=O)N2[C@H]1C(O)=O.CC(S[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)C.[C:40]([OH:50])(=[O:49])[C@H:41]([C:43]1[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=1)[OH:42]>>[CH3:1][O:49][C:40](=[O:50])[C@@H:41]([C:43]1[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=1)[OH:42]Participants
Procedure
The transformed strain XL10-Gold (pTrcFadLPL) prepared in Example 3 was inoculated again in 250 mL Erlenmeyer flask including 100 mL of LB liquid medium containing 50 μg/L of ampicillin, and then cultured at 37° C. Gene expression was induced by adding 0.1 mM of IPTG, when absorbance was 0.5 at 600 nm wavelength by spectrophotometer. 5 hours after inducing the expression, culture broth was centrifuged at 4° C., 600 rpm for 5 minutes to collect cells, and then, the collected cells were washed with 50 mM Tris-HCl solution (pH 8.0), followed by resuspending in 3 mL of buffer. Said re-suspension was put into a 10 mL flask, to which 30 mg of racemic mandelic acid methyl ester was added and allowed to react for 48 hours with stirring. Then, the suspension was centrifuged at 4° C. and 6000 rpm for 5 minutes to remove cells. The supernatant was collected and adjusted to a pH of 3.0. After extraction of the supernatant with 10 mL of ethyl acetate and hexane, the extract was analyzed by liquid chromatography. The analysis results showed that (S)-mandelic acid and (R)-mandelic acid methyl ester were obtained.
Workup
- customcultured at 37° C
- custom5 hours
- customwas centrifuged at 4° C.
- custom600 rpm for 5 minutes to collect cells
- washthe collected cells were washed with 50 mM Tris-HCl solution (pH 8.0)
- customwas put into a 10 mL flask, to which 30 mg of racemic mandelic acid methyl ester
- additionwas added
- customto react for 48 hours
- customwas centrifuged at 4° C.
- custom6000 rpm for 5 minutes to remove cells
- customThe supernatant was collected
- extractionAfter extraction of the supernatant with 10 mL of ethyl acetate and hexane
- customThe analysis results
Sources & evidence
- ORD record
- ord-a8c107d4348d4a3aba891e245f5578fd
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08158387B2
Reaction notes
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