化工社化工社 化学情報印刷レポート · 研究参考用
Methylene blue cation → 1H-Indolamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methylene blue cation | HCID 4139 | — |
| 反応物 | D-Tryptophan | HCID 9060 | — |
| 反応物 | HCID 178519208 | HCID 178519208 | — |
| 溶媒 | Potassium Phosphate, Tribasic | HCID 62657 | — |
| 生成物 | 1H-Indolamine | HCID 122074 | — |
反応手順
Human indoleamine 2,3-dioxygenasae (IDO) with an N-terminal His tag was expressed in E. coli and purified to homogeneity. IDO catalyzes the oxidative cleavage of the pyrrole ring of the indole nucleus of tryptophan to yield N′-formylkynurenine. The assays were performed at room temperature as described in the literature using 95 nM IDO and 2 mM D-Trp in the presence of 20 mM ascorbate, 5 μM methylene blue and 0.2 mg/mL catalase in 50 mM potassium phosphate buffer (pH 6.5). The initial reaction rates were recorded by continuously following the absorbance increase at 321 nm due to the formation of N′-formlylkynurenine (See: Sono, M., et al., 1980, J. Biol. Chem. 255, 1339-1345).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08822511B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-e9c2aa91fd504d05a76864c21cf0a5fa |
| 出典メモ | uspto-grants-2014_09 |