反応式
[S:1]([O-:4])([O-:3])=[O:2].[Na+:5].[Na+].[S:7](S([O-])=O)([O-:10])(=[O:9])=[O:8].[Na+].[Na+].[NH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][NH2:25].Cl.S(=O)(O)[O-].[Na+].NC(N)=CCCCCCC>O>[S:1](=[O:2])([OH:4])[O-:3].[Na+:5].[S:7](=[O:8])([OH:10])[O-:9].[CH2:21]([CH2:22][CH2:23][CH2:24][NH2:25])[CH2:20][CH2:19][CH2:18][CH2:17][NH2:16]参加物
反応条件
- 温度
- 100 °C
実験手順
Sodium bisulfite was prepared by adding 3.15 g of sodium sulfite and 7.15 g of sodium metabisulfite to 25 ml of water. 1,8-Diaminooctane (7.2 g) was added and the pH was adjusted to 7 with concentrated hydrochloric acid. Calf thymus DNA (Sigma, 139 mg) was dissolved in 20 mL of water and denatured by heating to 100° C. for 30 min followed by rapid cooling in an ice bath. The single stranded DNA was then sonicated for 40 min at 0° C. and added to the sodium bisulfite-diaminooctene solution. This gave a final concentration of 2 M bisulfite and 1 M diaminooctane. The mixture was clarified by centrifugation (4000×g) and then stirred at 60° C. (oil bath) for 42 hrs. The reaction mixture was cooled and filtered (0.2 μm filter) to remove a small amount of particulate material. The product was desalted in two 25 mL portions over a BioRad P-4 column (340×2.6 cm) equilibrated in 0.02 M sodium chloride, 1 mM EDTA, pH 8. After the void volume (60 mL), the product was collected in the next 50 mL fraction and each of these two fractions was separately dialyzed overnight against 4 L of water and lyphilized, yielding together 99.5 mg (72%). Seventy-five percent of the cytosine residues were substituted with DAO, based on alkaline hydrolysis-HPLC.
後処理
- temperatureby rapid cooling in an ice bath
- customwas then sonicated for 40 min at 0° C.
出典と根拠
- ORDレコード
- ord-2bd6678b5a6d4189904ee00c02b05a20
- 出典データセット
- uspto-grants-1997_07
- 特許番号
- US05650270
関連ノート
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