참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Oxoglutaric Acid | HCID 51 | — |
| 반응물 | L-Lysine | HCID 5962 | — |
| 반응물 | L-Valine | HCID 6287 | — |
| 반응물 | L-Isoleucine | HCID 6306 | — |
| 반응물 | 4-(2-Hydroxyethyl)-1-piperazineethanesulfonic acid | HCID 23831 | — |
| 반응물 | L-Glutamic Acid | HCID 33032 | — |
| 반응물 | L-Ascorbic Acid | HCID 54670067 | — |
| 생성물 | 4-Hydroxyisoleucine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08367382B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
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| ORD ID | ord-eb25dca2d1d14ea28fefb8291ea774c1 |
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| 출처 메모 | uspto-grants-2013_02 |
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