Wiame Elsa, Lamosa Pedro, Santos Helena, Van Schaftingen Emile
Laboratory of Physiological Chemistry, Université Catholique de Louvain and the Christian de Duve Institute of Cellular Pathology, Avenue Hippocrate 75, B-1200 Brussels, Belgium.
Biochem J. 2005 Dec 1;392(Pt 2):263-9. doi: 10.1042/BJ20051183.
The metabolism of the glycation product fructose-epsilon-lysine in Escherichia coli involves its ATP-dependent phosphorylation by a specific kinase (FrlD), followed by the conversion of fructoselysine 6-phosphate into glucose 6-phosphate and lysine by fructoselysine-6-phosphate deglycase (FrlB), which is distantly related to the isomerase domain of glucosamine-6-phosphate synthase. As shown in the present work, several bacterial operons comprise: (1) a homologue of fructoselysine-6-phosphate deglycase; (2) a second homologue of the isomerase domain of glucosamine-6-phosphate synthase, more closely related to it; and (3) components of a novel phosphotransferase system, but no FrlD homologue. The FrlB homologue (GfrF) and the closer glucosamine-6-phosphate synthase homologue (GfrE) encoded by an Enterococcus faecium operon were expressed in E. coli and purified. Similar to FrlB, GfrF catalysed the reversible conversion of fructoselysine 6-phosphate into glucose 6-phosphate and lysine. When incubated with fructose 6-phosphate and elevated concentrations of lysine, GfrE catalysed the formation of a compound identified as 2-epsilon-lysino-2-deoxy-6-phospho-glucose (glucoselysine 6-phosphate) by NMR. GfrE also catalysed the reciprocal conversion, i.e. the formation of fructose 6-phosphate (but not glucose 6-phosphate) from glucoselysine 6-phosphate. The equilibrium constant of this reaction (0.8 M) suggests that the enzyme serves to degrade glucoselysine 6-phosphate. In conclusion, GfrF and GfrE serve to metabolize glycation products formed from lysine and glucose (fructoselysine) or fructose (glucoselysine), via their 6-phospho derivatives. The latter are presumably formed by the putative phosphotransferase system encoded by gfrA-gfrD. The designation gfr (glycation and fructation product degradation) is proposed for this operon. This is the first description of an enzyme participating in the metabolism of fructation products.
大肠杆菌中糖化产物果糖-ε-赖氨酸的代谢过程包括:首先由一种特异性激酶(FrlD)将其进行ATP依赖的磷酸化,随后果糖赖氨酸6-磷酸通过果糖赖氨酸-6-磷酸脱糖基酶(FrlB)转化为葡萄糖6-磷酸和赖氨酸,FrlB与氨基葡萄糖-6-磷酸合酶的异构酶结构域有较远的亲缘关系。如本研究所示,几个细菌操纵子包含:(1)果糖赖氨酸-6-磷酸脱糖基酶的同源物;(2)与氨基葡萄糖-6-磷酸合酶异构酶结构域关系更密切的第二个同源物;(3)一种新型磷酸转移酶系统的组分,但没有FrlD同源物。粪肠球菌操纵子编码的FrlB同源物(GfrF)和关系更密切的氨基葡萄糖-6-磷酸合酶同源物(GfrE)在大肠杆菌中表达并纯化。与FrlB相似,GfrF催化果糖赖氨酸6-磷酸可逆转化为葡萄糖6-磷酸和赖氨酸。当与果糖6-磷酸和高浓度赖氨酸一起温育时,GfrE通过核磁共振催化形成一种被鉴定为2-ε-赖氨酸基-2-脱氧-6-磷酸葡萄糖(葡萄糖赖氨酸6-磷酸)的化合物。GfrE还催化了反向转化,即从葡萄糖赖氨酸6-磷酸形成果糖6-磷酸(但不是葡萄糖6-磷酸)。该反应的平衡常数(0.8 M)表明该酶用于降解葡萄糖赖氨酸6-磷酸。总之,GfrF和GfrE通过其6-磷酸衍生物来代谢由赖氨酸和葡萄糖(果糖赖氨酸)或果糖(葡萄糖赖氨酸)形成的糖化产物。后者可能由gfrA - gfrD编码的假定磷酸转移酶系统形成。建议将该操纵子命名为gfr(糖化和果糖化产物降解)。这是对参与果糖化产物代谢的一种酶的首次描述。