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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630578Generated: October 26, 2026

Ampicillin → (R)-4-cyano-3-hydroxybutyric acid

https://huagongshe.com/reaction/630578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmpicillinHCID 6249—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactantisopropyl beta-D-thiogalactopyranosideHCID 656894—
SolventEthyl AcetateHCID 8857—
Product(R)-4-cyano-3-hydroxybutyric acidHCID 10236005—

Reaction Steps

Putative nitrilase up-mutants were assayed in triplicate. Each transformant was grown in 5 mL LB (100 μg/mL ampicillin), at 37° C., 220 rpm for 18 h. The overnight culture was diluted 2-fold and nitrilase expression induced at 37° C., 220 rpm with 0.1 mM IPTG for 6 h. Cells were harvested by centrifugation, washed in 100 mM pH 7 sodium phosphate buffer and then re-suspended in 1 mL of 100 mM HGN in 100 mM pH 7 sodium phosphate buffer. Reactions were allowed to proceed for at least 36 h at 22° C. with gentle agitation. Reaction progress was monitored by TLC (1:1 EtOAc:Hexanes, Rf=0.5, nitrile; Rf=0.0, acid). Cells and other debris were removed by centrifugation and the treated with one volume methanol prior to lyophilization. The lyophilizate was re-suspended in methanol and treated with TMS-diazomethane (10 equivalents, 2 M solution in hexanes) until gas evolution ceased and yellow color persisted in order to prepare the methyl ester for GC analysis. Selected nitrilase variants producing (R)-(−)-3-hydroxy-4-cyanobutyric acid of 95% ee or greater were then evaluated for performance at 2.25 M HGN.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315792B2
Source datasetuspto-grants-2016_04
ORD IDord-dc2cb9cbbded44018f8ebf5f27125bb3
Source noteuspto-grants-2016_04