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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640384Generated: October 26, 2026

2-Oxoglutaric Acid → 4-Hydroxyisoleucine

https://huagongshe.com/reaction/1640384

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Oxoglutaric AcidHCID 51—
ReactantL-LysineHCID 5962—
ReactantL-ValineHCID 6287—
ReactantL-IsoleucineHCID 6306—
Reactant4-(2-Hydroxyethyl)-1-piperazineethanesulfonic acidHCID 23831—
ReactantL-Glutamic AcidHCID 33032—
ReactantL-Ascorbic AcidHCID 54670067—
Product4-HydroxyisoleucineHCID 2773624—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114651B2
Source datasetuspto-grants-2012_02
ORD IDord-fb6cb9f63ff84222930ce0e72f529b5e
Source noteuspto-grants-2012_02