戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1434491作成日:2026年10月27日

5'-Atp → (R)-3-hydroxyoctanoyl-CoA

https://huagongshe.com/reaction/1434491

反応式

関与物質

役割名称HCID仕込み量
反応物5'-AtpHCID 5957—
反応物Coenzyme AHCID 87642—
反応物Magnesium ChlorideHCID 5360315—
反応物(R)-3-hydroxyoctanoateHCID 86308678—
反応物(R)-3-Hydroxy-5-(4-fluorophenyl)valeryl-CoAHCID 86588297—
生成物(R)-3-hydroxyoctanoyl-CoAHCID 11966193—

反応手順

(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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07615233B2
出典データセットuspto-grants-2009_11
ORD IDord-48431586237a4b14b9107c0f4f03c510
出典メモuspto-grants-2009_11