Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Oxoglutaric Acid | HCID 51 | — |
| Reactant | L-Lysine | HCID 5962 | — |
| Reactant | L-Valine | HCID 6287 | — |
| Reactant | L-Isoleucine | HCID 6306 | — |
| Reactant | 4-(2-Hydroxyethyl)-1-piperazineethanesulfonic acid | HCID 23831 | — |
| Reactant | L-Glutamic Acid | HCID 33032 | — |
| Reactant | L-Ascorbic Acid | HCID 54670067 | — |
| Product | 4-Hydroxyisoleucine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08114651B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-fb6cb9f63ff84222930ce0e72f529b5e |
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| Source note | uspto-grants-2012_02 |
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