関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Fluoride | HCID 5235 | — |
| 反応物 | NADPH | HCID 5884 | — |
| 反応物 | Lacto-N-biose | HCID 440994 | — |
| 反応物 | HCID 178434963 | HCID 178434963 | — |
| 反応物 | HCID 178508932 | HCID 178508932 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | beta-D-Galp-(1->3)-(alpha-L-Fucp-(1->4))-D-GlcpNAc | HCID 22806751 | — |
反応手順
A mixture of GTP Na salt (6.0 mg, 10 μmol), Man-1-P K salt (3.5 mg, 10 μmol), Galβ1,3GlcNAc (3.8 mg, 10 μmol), NaF (0.42 mg, 10 μmol), NADPH (9.4 mg, 10 μmol), PEP K salt (4.1 mg, 20 μmol), MgCl2-6H2O (2.6 mg, 10 μmol), MnCl2-4H2O (2 mg, 10 μmol), 2-propanol (50 μL), ADH (12 U), PK (200 U), PPase (100 U), crude enzyme preparation of GDP-mannose pyrophosphorylase (1.0 mL), and crude enzyme preparation of GDP-Fuc producing enzyme (1.0 mL) in 100 mM tris buffer (pH 7.5) and diluted to 3 mL. α1,3/4-Fucosyltransferase (0.01 U) was added to the mixture and the resulting mixture was stirred under Ar for three days at room temperature. The mixture was filtered and the filtrate was applied to a column of Dowex 1-X8 (OH−) form followed with a column of Dowex 50W-X8 [H+] with water. The fractions were collected and lyophilized. The residual material was purified with a column of Sephadex G-25 (superfine) with water. The appropriate fractions were pooled and lyophilized to give Galβ1,3(Fucα1,4)GlcNAc. Its 1H-NMR spectrum was in good agreement with that reported. [Dumas et al., Biomed. Chem. Lett., 1:425 (1991).]
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07335500B2 |
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| 出典データセット | uspto-grants-2008_02 |
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| ORD ID | ord-d3ce4051b17a4f8ebcc5a7fa5867c3d2 |
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| 出典メモ | uspto-grants-2008_02 |
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