Oh Jongmin, Lee Sun-Gu, Kim Byung-Gee, Sohng Jae Kyung, Liou Kwangkyoung, Lee Hei Chan
Institute of Molecular Biology and Genetics and School of Chemical Engineering, Seoul National University, Seoul 151-742, South Korea.
Biotechnol Bioeng. 2003 Nov 20;84(4):452-8. doi: 10.1002/bit.10789.
An enzymatic production method for dTDP-4-keto-6-deoxy-D-glucose, a key intermediate of various deoxysugars in antibiotics, was developed starting from dTMP, acetyl phosphate, and glucose-1-phosphate. Four enzymes, i.e., TMP kinase, acetate kinase, dTDP-glucose synthase, and dTDP-D-glucose 4,6-dehydratase' were overexpressed using T7 promoter system in the E. coli BL21 strain, and the dTDP-4-keto-6-deoxy-D-glucose was synthesized by using the enzyme extracts in one-pot batch system. When 20 mM dTMP of initial concentration was used, Mg2+ ion, acetyl phosphate, and glucose-1-phosphate concentrations were optimized. About 95% conversion yield of dTDP-4-keto-6-deoxy-D-glucose was obtained based on initial dTMP concentration at 20 mM dTMP, 1 mM ATP, 60 mM acetyl phosphate, 80 mM glucose-1-phosphate, and 20 mM MgCl(2). The rate-limiting step in this multiple enzyme reaction system was the dTDP-glucose synthase reaction. Using the reaction scheme, about 1 gram of purified dTDP-4-keto-6-deoxy-D-glucose was obtained in an overall yield of 81% after two-step purification, i.e., anion exchange chromatography and gel filtration.
以dTMP、乙酰磷酸和葡萄糖-1-磷酸为原料,开发了一种酶法生产dTDP-4-酮基-6-脱氧-D-葡萄糖的方法,dTDP-4-酮基-6-脱氧-D-葡萄糖是抗生素中各种脱氧糖的关键中间体。使用T7启动子系统在大肠杆菌BL21菌株中过表达了四种酶,即TMP激酶、乙酸激酶、dTDP-葡萄糖合酶和dTDP-D-葡萄糖4,6-脱水酶,并在一锅分批系统中使用酶提取物合成了dTDP-4-酮基-6-脱氧-D-葡萄糖。当使用初始浓度为20 mM的dTMP时,对Mg2+离子、乙酰磷酸和葡萄糖-1-磷酸的浓度进行了优化。在20 mM dTMP、1 mM ATP、60 mM乙酰磷酸、80 mM葡萄糖-1-磷酸和20 mM MgCl₂的条件下,基于初始dTMP浓度,dTDP-4-酮基-6-脱氧-D-葡萄糖的转化率约为95%。该多酶反应体系中的限速步骤是dTDP-葡萄糖合酶反应。根据该反应方案,经过两步纯化,即阴离子交换色谱和凝胶过滤,得到了约1克纯化的dTDP-4-酮基-6-脱氧-D-葡萄糖,总产率为81%。