Department of Chemistry, University of Georgia, Athens, GA, USA.
Department of Biochemistry and Molecular Biology, University of Georgia, Athens, GA, USA.
FEBS Lett. 2022 Sep;596(18):2441-2448. doi: 10.1002/1873-3468.14469. Epub 2022 Aug 29.
d-Glucosaminate-6-phosphate ammonia-lyase (DGL) catalyzes the conversion of d-glucosaminate-6-phosphate to 2-keto-3-deoxyglutarate-6-phosphate, with stereospecific protonation of C-3 of the product. The crystal structure of DGL showed that His-163 could serve as the proton donor. H163A mutant DGL is fully active in the steady-state reaction, and the pre-steady-state kinetics are very similar to those of wild-type DGL. However, H163A DGL accumulates a transient intermediate with λ at 293 nm during the reaction that is not seen with wild-type DGL. Furthermore, NMR analysis of the reaction of H163A DGL in D O shows that the product is a mixture of deuterated diastereomers at C-3. These results establish that His-163 is the proton donor in the reaction mechanism of DGL.
葡糖胺-6-磷酸氨裂解酶(DGL)催化葡糖胺-6-磷酸转化为 2-酮-3-脱氧葡糖酸-6-磷酸,产物的 C-3 进行立体特异性质子化。DGL 的晶体结构表明 His-163 可以作为质子供体。H163A 突变型 DGL 在稳态反应中完全具有活性,且预稳态动力学与野生型 DGL 非常相似。然而,在反应过程中,H163A DGL 会积累一个在 293nm 处有 λ 的瞬态中间体,而野生型 DGL 则不会出现这种中间体。此外,对 H163A DGL 在 D2O 中的反应的 NMR 分析表明,产物是 C-3 处的氘代非对映异构体的混合物。这些结果证实 His-163 是 DGL 反应机制中的质子供体。