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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 383221생성일: 2026년 10월 26일

2-Oxoglutaric Acid → 4-Hydroxyisoleucine

https://huagongshe.com/reaction/383221

반응식

참여 물질

역할이름HCID투입량
반응물2-Oxoglutaric AcidHCID 51—
반응물L-LysineHCID 5962—
반응물L-ValineHCID 6287—
반응물L-IsoleucineHCID 6306—
반응물4-(2-Hydroxyethyl)-1-piperazineethanesulfonic acidHCID 23831—
반응물L-Glutamic AcidHCID 33032—
반응물L-Ascorbic AcidHCID 54670067—
생성물4-HydroxyisoleucineHCID 2773624—

반응 단계

By using a cell lysate prepared from 2-e-2 cells at OD660 of 7 according to the method described in <5>, the reaction characteristics for various amino acids were evaluated. The cell lysate and a substrate solution were mixed, then the reaction proceeded at 30° C. for 1 hour, and the production of new substances was evaluated by TLC or amino acid analysis. The substrate reaction mixture contained 5 mM amino acid, 5 mM Fe2+, 5 mM 2-oxoglutaric acid, 5 mM ascorbic acid, and 100 mM HEPES (pH 7). In addition to L-isoleucine, the amino acids L-leucine, L-valine, L-glutamic acid, and L-lysine were each individually evaluated. The 4-hydroxyisoleucine which was produced was analyzed by the method described in Example 1. The results are shown in Table 6. Production of amino acids other than L-isoleucine was not observed. Therefore, it was suggested that this enzyme was an isoleucine-specific dioxygenase.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367382B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-eb25dca2d1d14ea28fefb8291ea774c1
출처 메모uspto-grants-2013_02