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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988527Generated: October 27, 2026

Oxygen → Acetate

https://huagongshe.com/reaction/1988527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
Reactant3-Dehydroquinic AcidHCID 439351—
ReactantHCID 178524980HCID 178524980—
ProductAcetateHCID 175—
ProductHCID 178524980HCID 178524980—

Reaction Steps

QP1.1/pKD12.112 was cultured for 60 h under fed-batch fermentor conditions at 37° C., pH 7.0, dissolved oxygen at 10% of saturation and an initial glucose concentration of 23 g/L. Extracellular accumulation of quinic acid began in early to mid log phase of microbial growth as represented by the open boxes in FIG. 2. The dry cell weight is represented by the solid line and closed circles. 3-Dehydroquinate was efficiently converted to quinic acid as there was never a build-up of the intermediate (solid bars in FIG. 2). After 60 hours of cultivation with Kc=0.1, E. coli QP1.1/pKD12.112 synthesized 60 g/L of quinic acid in 23% yield along with only 2.6 g of 3-dehydroquinate. Quinic acid was isolated from the fermentation broth by ion-exchange chromatography on AG1-x8 (acetate form) and Dowex 50 (H+ form) columns. Purified quinic acid was obtained by further recrystallization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642083B2
Source datasetuspto-grants-2010_01
ORD IDord-49150dfec7454a669b9b7c1242798a66
Source noteuspto-grants-2010_01