Department of Chemistry and Biochemistry, Miami University, Oxford, Ohio 45056, United States.
Biochemistry. 2011 Mar 8;50(9):1442-53. doi: 10.1021/bi101932s. Epub 2011 Feb 14.
GmACP3 from Geobacter metallireducens is a specialized acyl carrier protein (ACP) whose gene, gmet_2339, is located near genes encoding many proteins involved in lipopolysaccharide (LPS) biosynthesis, indicating a likely function for GmACP3 in LPS production. By overexpression in Escherichia coli, about 50% holo-GmACP3 and 50% apo-GmACP3 were obtained. Apo-GmACP3 exhibited slow precipitation and non-monomeric behavior by (15)N NMR relaxation measurements. Addition of 4'-phosphopantetheine (4'-PP) via enzymatic conversion by E. coli holo-ACP synthase resulted in stable >95% holo-GmACP3 that was characterized as monomeric by (15)N relaxation measurements and had no indication of conformational exchange. We have determined a high-resolution solution structure of holo-GmACP3 by standard NMR methods, including refinement with two sets of NH residual dipolar couplings, allowing for a detailed structural analysis of the interactions between 4'-PP and GmACP3. Whereas the overall four helix bundle topology is similar to previously solved ACP structures, this structure has unique characteristics, including an ordered 4'-PP conformation that places the thiol at the entrance to a central hydrophobic cavity near a conserved hydrogen-bonded Trp-His pair. These residues are part of a conserved WDSLxH/N motif found in GmACP3 and its orthologs. The helix locations and the large hydrophobic cavity are more similar to medium- and long-chain acyl-ACPs than to other apo- and holo-ACP structures. Taken together, structural characterization along with bioinformatic analysis of nearby genes suggests that GmACP3 is involved in lipid A acylation, possibly by atypical long-chain hydroxy fatty acids, and potentially is involved in synthesis of secondary metabolites.
来自 Geobacter metallireducens 的 GmACP3 是一种特殊的酰基载体蛋白 (ACP),其基因 gmet_2339 位于编码许多参与脂多糖 (LPS) 生物合成的蛋白质的基因附近,表明 GmACP3 在 LPS 生产中可能具有作用。通过在大肠杆菌中的过表达,获得了约 50%的全同型 GmACP3 和 50%的去辅基 GmACP3。通过 (15)N NMR 弛豫测量,去辅基 GmACP3 表现出缓慢沉淀和非单体行为。通过大肠杆菌全同型 ACP 合酶的酶促转化添加 4'-磷酸泛酰巯基乙胺 (4'-PP),导致稳定的>95%的全同型 GmACP3,通过 (15)N 弛豫测量表现为单体,并且没有构象交换的迹象。我们通过标准 NMR 方法确定了全同型 GmACP3 的高分辨率溶液结构,包括用两组 NH 残基偶极耦合进行精修,允许对 4'-PP 和 GmACP3 之间的相互作用进行详细的结构分析。尽管整体的四螺旋束拓扑结构与以前解决的 ACP 结构相似,但该结构具有独特的特征,包括有序的 4'-PP 构象,将硫醇置于靠近保守的氢键结合色氨酸-组氨酸对的中央疏水性腔的入口处。这些残基是在 GmACP3 及其同源物中发现的保守 WDSLxH/N 基序的一部分。螺旋位置和大疏水性腔与中链和长链酰基-ACP 更相似,而与其他去辅基和全同型 ACP 结构不同。综上所述,结构特征以及附近基因的生物信息学分析表明,GmACP3 参与脂质 A 的酰化,可能通过非典型的长链羟基脂肪酸,并且可能参与次生代谢物的合成。