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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1019491생성일: 2026년 10월 27일

L-Alanine → Acetylpyruvate

https://huagongshe.com/reaction/1019491

반응식

참여 물질

역할이름HCID투입량
반응물L-AlanineHCID 5950—
반응물L-(-)-OrnithineHCID 6262—
반응물acetyl CoAHCID 444493—
반응물AcetylpyruvateHCID 5459760—
반응물AcetylacrylateHCID 11083863—
반응물Penta-2,4-dienoateHCID 73155734—
생성물AcetylpyruvateHCID 5459760—
생성물4-Hydroxy-2-oxopentanoateHCID 9543038—
생성물2-Hydroxy-4-oxopentanoateHCID 20514168—

반응 단계

FIG. 13 shows pathways from alanine or ornithine to 2,4-pentadienoate. In Step A of FIG. 13, alanine and acetyl-CoA are joined by AKP thiolase to form AKP. In one pathway, AKP is deaminated to acetylacrlate (Step B). The 4-oxo group of acetylacrylate is then reduced and dehydrated to 2,4-pentadienoate (Steps C/D). In an alternative pathway, AKP is converted to 2,4-dioxopentanoate by an aminotransferase or dehydrogenase (Step E). Reduction of the 2- or 4-oxo group of 2,4-dioxopentanoate yields 2-hydroxy-4-oxopentanoate (Step H) or 4-hydroxy-2-oxovalerate (Step K), respectively. 4-Hydroxy-2-oxovalerate can alternately be formed by the reduction of AKP to 2-amino-4-hydroxypentanoate (Step J) followed by transamination or oxidative deamination (Step L). Once formed, 4-hydroxy-2-oxovalerate can be converted to 2,4-pentadienoate in three enzymatic steps as shown in FIG. 12 (Steps B/C/D of FIG. 12). The 2-hydroxy-4-oxopentanoate intermediate can undergo dehydration to acetylacrylate (Step F) followed by reduction and dehydration (Steps C/D).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08715957B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-a9e81385edd246a0915772614e6330c8
출처 메모uspto-grants-2014_05