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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434491Generated: October 26, 2026

5'-Atp → (R)-3-hydroxyoctanoyl-CoA

https://huagongshe.com/reaction/1434491

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5'-AtpHCID 5957—
ReactantCoenzyme AHCID 87642—
ReactantMagnesium ChlorideHCID 5360315—
Reactant(R)-3-hydroxyoctanoateHCID 86308678—
Reactant(R)-3-Hydroxy-5-(4-fluorophenyl)valeryl-CoAHCID 86588297—
Product(R)-3-hydroxyoctanoyl-CoAHCID 11966193—

Reaction Steps

(R)-3-hydroxyoctanoyl-CoA was synthesized according to Rehm B H A, Kruger N, Steinbuchel A (1998) Journal of Biological Chemistry 273 pp 24044-24051 with certain changes. Acyl-CoA synthetase (Sigma Co.) was dissolved in trishydrochloric acid buffer (50 mM, pH 7.5) containing 2 mM ATP, 5 mM MgCl2, 2 mM coenzyme A and 2 mM (R)-3-hydroxyoctanoate to a concentration of 0.1 mU/μL. It was retained in a bath of 37° C. and was sampled suitably and the proceeding of reaction was analyzed by HPLC. After the enzyme reaction was terminated by adding sulfuric acid to 0.02 N to the sampled reaction liquid, the unreacted substrate (R)-3-hydroxyoctganoate was removed by extraction with n-heptane. The HPLC analysis employed RP18 column (nucleosil C18, 7 μm, Knauser), and elusion was made under a linear concentration slope of acetonitrile, utilizing 25 mM phosphoric acid buffer (pH 5.3) as the moving phase, and the thioester compound generated by the enzymatic reaction was detected by monitoring the absorption spectrum of 200 to 500 nm with a diode array detector. (R)-3-hydroxy-5-phenylvaryl CoA and (R)-3-hydroxy-5-(4-fluorophenyl)valeryl CoA were also synthesized in a similar manner.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615233B2
Source datasetuspto-grants-2009_11
ORD IDord-48431586237a4b14b9107c0f4f03c510
Source noteuspto-grants-2009_11