Enzymatic Synthesis of ATP Analogs and Their Purification by Reverse-Phase High-Performance Liquid Chromatography

✍ Scribed by B. Schobert

• Publisher: Elsevier Science
• Year: 1995
• Tongue: English
• Weight: 398 KB
• Volume: 226
• Category: Article
• ISSN: 0003-2697
• DOI: 10.1006/abio.1995.1227

✦ Synopsis

The enzymatic syntheses of ATP analogs, such as tubercidin 5 '-triphosphate, formycin A 5 '-triphosphate, and etheno-ATP, from their respective mono- and diphosphate are described. The reaction products were purified by reverse-phase HPLC using a C-18 matrix and a volatile mobile phase at (\mathrm{pH} 7), with tributylamine as the ion-pairing agent. Each of the analogs required a buffer of somewhat different composition for the baseline separation of reaction product and reactants. The elutions were isocratic and allowed several successive runs without any intermediate equilibration of the column. After freeze-drying of the pooled fractions, the yield of the synthesized nucleoside triphosphate was approximately (70 %). The described procedures are applicable either for analytical investigations or for semipreparative purposes. (\approx 1995) Academic Press, Inc.