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化工社化工社 化学情報印刷レポート · 研究参考用
HRID 389838作成日:2026年10月27日

Chloramphenicol → Methyl Lactate

https://huagongshe.com/reaction/389838

反応式

関与物質

役割名称HCID仕込み量
反応物ChloramphenicolHCID 5959—
反応物AmpicillinHCID 6249—
反応物4-HydroxybutanoateHCID 3037032—
反応物3-HydroxypropionateHCID 5459847—
生成物Methyl LactateHCID 11040—
生成物Butanoic acid, 4-hydroxy-, methyl esterHCID 70217—
生成物Propanoic acid, 3-hydroxy-, methyl esterHCID 80252—
生成物4-Hydroxybutyrate 3-hydroxypropionate lactateHCID 86645087—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383379B2
出典データセットuspto-grants-2013_02
ORD IDord-2c4161ef867a4cf4a9cfaee7a1d65950
出典メモuspto-grants-2013_02