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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 389838생성일: 2026년 10월 26일

Chloramphenicol → Methyl Lactate

https://huagongshe.com/reaction/389838

반응식

참여 물질

역할이름HCID투입량
반응물ChloramphenicolHCID 5959—
반응물AmpicillinHCID 6249—
반응물4-HydroxybutanoateHCID 3037032—
반응물3-HydroxypropionateHCID 5459847—
생성물Methyl LactateHCID 11040—
생성물Butanoic acid, 4-hydroxy-, methyl esterHCID 70217—
생성물Propanoic acid, 3-hydroxy-, methyl esterHCID 80252—
생성물4-Hydroxybutyrate 3-hydroxypropionate lactateHCID 86645087—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383379B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-2c4161ef867a4cf4a9cfaee7a1d65950
출처 메모uspto-grants-2013_02