Lee Hei Chan, Lee Seung-Don, Sohng Jae Kyung, Liou Kwangkyoung
Institute of Biomolecule Reconstruction, Sun Moon University, Chungnam 336-708, Korea.
J Biochem Mol Biol. 2004 Jul 31;37(4):503-6. doi: 10.5483/bmbrep.2004.37.4.503.
Glucose-1-phosphate uridylyltransferase from E. coli K12 was used to convert uridine-5'-triphosphate and glucose-1-phosphate to UDP-D-glucose. The conversion was efficient and completed within 5 minutes under the employed conditions. In addition, thymidine-5'-monophosphate kinase and acetate kinase were proven to be non-specific, converting udridine-5'-monophosphate to uridine-5'-triphosphate with 55% conversion after 6 h, which was much slower than the production of TTP under the same conditions (complete conversion within one hour). Since these two reactions could proceed under the same conditions, a one-pot synthesis of UDP-D-glucose with ATP regeneration was designed from easily available starting materials, and conversion up to 40% by HPLC peak integration was achieved given a reaction time of 4 h.
来自大肠杆菌K12的葡萄糖-1-磷酸尿苷酰转移酶被用于将尿苷-5'-三磷酸和葡萄糖-1-磷酸转化为UDP-D-葡萄糖。在所采用的条件下,该转化效率很高,在5分钟内即可完成。此外,胸苷-5'-单磷酸激酶和乙酸激酶被证明是非特异性的,在6小时后将尿苷-5'-单磷酸转化为尿苷-5'-三磷酸的转化率为55%,这比在相同条件下三磷酸胸苷的生成速度要慢得多(1小时内完全转化)。由于这两个反应可以在相同条件下进行,因此设计了一种从易于获得的起始原料一锅法合成UDP-D-葡萄糖并实现ATP再生的方法,在4小时的反应时间内,通过HPLC峰面积积分实现了高达40%的转化率。