Department of Molecular and Cellular Biochemistry, University of Kentucky College of Medicine, Lexington, Kentucky 40536, USA.
J Biol Chem. 2010 Jan 15;285(3):1671-80. doi: 10.1074/jbc.M109.061630. Epub 2009 Nov 18.
Escherichia coli strain O157 produces an O-antigen with the repeating tetrasaccharide unit alpha-D-PerNAc-alpha-l-Fuc-beta-D-Glc-alpha-D-GalNAc, preassembled on undecaprenyl pyrophosphate (Und-P-P). These studies were conducted to determine whether the biosynthesis of the lipid-linked repeating tetrasaccharide was initiated by the formation of GalNAc-P-P-Und by WecA. When membrane fractions from E. coli strains K12, O157, and PR4019, a WecA-overexpressing strain, were incubated with UDP-[3H]GalNAc, neither the enzymatic synthesis of [3H]GlcNAc-P-P-Und nor [3H]GalNAc-P-P-Und was detected. However, when membrane fractions from strain O157 were incubated with UDP-[3H]GlcNAc, two enzymatically labeled products were observed with the chemical and chromatographic properties of [3H]GlcNAc-P-P-Und and [3H]GalNAc-P-P-Und, suggesting that strain O157 contained an epimerase capable of interconverting GlcNAc-P-P-Und and GalNAc-P-P-Und. The presence of a novel epimerase was demonstrated by showing that exogenous [3H]GlcNAc-P-P-Und was converted to [3H]GalNAc-P-P-Und when incubated with membranes from strain O157. When strain O157 was metabolically labeled with [3H]GlcNAc, both [3H]GlcNAc-P-P-Und and [3H]GalNAc-P-P-Und were detected. Transformation of E. coli strain 21546 with the Z3206 gene enabled these cells to synthesize GalNAc-P-P-Und in vivo and in vitro. The reversibility of the epimerase reaction was demonstrated by showing that [3H]GlcNAc-P-P-Und was reformed when membranes from strain O157 were incubated with exogenous [3H]GalNAc-P-P-Und. The inability of Z3206 to complement the loss of the gne gene in the expression of the Campylobacter jejuni N-glycosylation system in E. coli indicated that it does not function as a UDP-GlcNAc/UDP-GalNAc epimerase. Based on these results, GalNAc-P-P-Und is synthesized reversibly by a novel GlcNAc-P-P-Und epimerase after the formation of GlcNAc-P-P-Und by WecA in E. coli O157.
大肠杆菌 O157 株产生具有重复四糖单元α-D-PerNAc-α-l-Fuc-β-D-Glc-α-D-GalNAc 的 O-抗原,该四糖单元预先组装在十一碳烯焦磷酸上(Und-P-P)。这些研究旨在确定 WecA 是否通过形成 GalNAc-P-P-Und 来启动脂质连接的重复四糖的生物合成。当用 UDP-[3H]GalNAc 孵育大肠杆菌 K12、O157 和 PR4019 菌株(一种 WecA 过表达菌株)的膜部分时,既没有检测到[3H]GlcNAc-P-P-Und 的酶促合成,也没有检测到[3H]GalNAc-P-P-Und。然而,当用 UDP-[3H]GlcNAc 孵育 O157 菌株的膜部分时,观察到两种具有化学和色谱性质的酶标记产物[3H]GlcNAc-P-P-Und 和[3H]GalNAc-P-P-Und,表明 O157 菌株含有一种能够使 GlcNAc-P-P-Und 和 GalNAc-P-P-Und 相互转化的差向异构酶。通过显示当用 O157 菌株的膜孵育时,外源[3H]GlcNAc-P-P-Und 被转化为[3H]GalNAc-P-P-Und,证明了新型差向异构酶的存在。当用[3H]GlcNAc 对 O157 菌株进行代谢标记时,既检测到[3H]GlcNAc-P-P-Und,也检测到[3H]GalNAc-P-P-Und。用 Z3206 基因转化大肠杆菌 21546 使这些细胞能够在体内和体外合成 GalNAc-P-P-Und。当用 O157 菌株的膜孵育外源[3H]GalNAc-P-P-Und 时,[3H]GlcNAc-P-P-Und 重新形成,证明了差向异构酶反应的可逆性。Z3206 不能补充 WecA 在大肠杆菌中表达空肠弯曲菌 N-糖基化系统时 gne 基因的缺失,表明它不能作为 UDP-GlcNAc/UDP-GalNAc 差向异构酶发挥作用。基于这些结果,在大肠杆菌 O157 中由 WecA 形成 GlcNAc-P-P-Und 后,通过一种新型的 GlcNAc-P-P-Und 差向异构酶可可逆地合成 GalNAc-P-P-Und。