Hecht S, Wungsintaweekul J, Rohdich F, Kis K, Radykewicz T, Schuhr C A, Eisenreich W, Richter G, Bacher A
Lehrstuhl für Organische Chemie und Biochemie, Technische Universität München, Lichtenbergstrasse 4, D-85747 Garching, Germany.
J Org Chem. 2001 Nov 16;66(23):7770-5. doi: 10.1021/jo015890v.
This paper describes the recombinant expression of the ispC gene of Escherichia coli specifying 2C-methyl-D-erythritol 4-phosphate synthase in a modified form that can be purified efficiently by metal-chelating chromatography. The enzyme was used for the preparation of isotope-labeled 2C-methyl-D-erythritol 4-phosphate employing isotope-labeled glucose and pyruvate as starting materials. The simple one-pot methods described afford numerous isotopomers of 2C-methyl-D-erythritol 4-phosphate carrying (3)H, (13)C, or (14)C from commercially available precursors. The overall yield based on the respective isotope-labeled starting material is approximately 50%.
本文描述了大肠杆菌ispC基因的重组表达,该基因编码的2C-甲基-D-赤藓糖醇4-磷酸合酶以一种修饰形式存在,可通过金属螯合色谱法高效纯化。该酶用于以同位素标记的葡萄糖和丙酮酸为起始原料制备同位素标记的2C-甲基-D-赤藓糖醇4-磷酸。所描述的简单一锅法可从市售前体中得到携带³H、¹³C或¹⁴C的多种2C-甲基-D-赤藓糖醇4-磷酸的同位素异构体。基于各自同位素标记的起始原料,总产率约为50%。