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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389838Generated: October 25, 2026

Chloramphenicol → Methyl Lactate

https://huagongshe.com/reaction/389838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloramphenicolHCID 5959—
ReactantAmpicillinHCID 6249—
Reactant4-HydroxybutanoateHCID 3037032—
Reactant3-HydroxypropionateHCID 5459847—
ProductMethyl LactateHCID 11040—
ProductButanoic acid, 4-hydroxy-, methyl esterHCID 70217—
ProductPropanoic acid, 3-hydroxy-, methyl esterHCID 80252—
Product4-Hydroxybutyrate 3-hydroxypropionate lactateHCID 86645087—

Reaction Steps

4-Hydroxybutyrate-3-hydroxypropionate-lactate terpolymer was prepared according to the method of example 2 except that the collected cells was anaerobically cultured for 3 days in MR medium further containing 2 g/L of 4-hydroxybutyrate (4-HB), 2 g/L of 3-hydroxypropionate (3-HP), 100 mg/L of ampicillin and 30 mg/L of chloramphenicol instead of MR medium further containing g/L of 4-HB, 100 mg/L of ampicillin and 30 mg/L of chloramphenicol. —As a result of the analysis, methyl-4-hydroxybutyrate, methyl-3-hydroxypropionate and methyl-lactate were detected in E. coli Top10/pPs619C1300-CPPCT/pMCSPtbBuk transformant, which meant that new 4-hydroxybutyrate-3-hydroxypropionate-lactate terpolymer [poly(4-hydroxybutyrate-co-3-hydroxypropionate-co-lactate)] was prepared by the recombinant E. Coli. 1H-NMR and GC-MSD results of the obtained 4-hydroxybutyrate-3-hydroxypropionate-lactate terpolymer were shown in FIGS. 6 and 7, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383379B2
Source datasetuspto-grants-2013_02
ORD IDord-2c4161ef867a4cf4a9cfaee7a1d65950
Source noteuspto-grants-2013_02