Robb Melissa, Robb Craig S, Higgins Melanie A, Hobbs Joanne K, Paton James C, Boraston Alisdair B
From the Department of Biochemistry and Microbiology, University of Victoria, Victoria, British Columbia, Canada V8W 3P6 and.
the Research Centre for Infectious Diseases, School of Biological Sciences, University of Adelaide, South Australia 5005, Australia.
J Biol Chem. 2015 Dec 25;290(52):30888-900. doi: 10.1074/jbc.M115.688630. Epub 2015 Oct 21.
An important facet of the interaction between the pathogen Streptococcus pneumoniae (pneumococcus) and its human host is the ability of this bacterium to process host glycans. To achieve cleavage of the glycosidic bonds in host glycans, S. pneumoniae deploys a wide array of glycoside hydrolases. Here, we identify and characterize a new family 20 glycoside hydrolase, GH20C, from S. pneumoniae. Recombinant GH20C possessed the ability to hydrolyze the β-linkages joining either N-acetylglucosamine or N-acetylgalactosamine to a wide variety of aglycon residues, thus revealing this enzyme to be a generalist N-acetylhexosaminidase in vitro. X-ray crystal structures were determined for GH20C in a ligand-free form, in complex with the N-acetylglucosamine and N-acetylgalactosamine products of catalysis and in complex with both gluco- and galacto-configured inhibitors O-(2-acetamido-2-deoxy-D-glucopyranosylidene)amino N-phenyl carbamate (PUGNAc), O-(2-acetamido-2-deoxy-D-galactopyranosylidene)amino N-phenyl carbamate (GalPUGNAc), N-acetyl-D-glucosamine-thiazoline (NGT), and N-acetyl-D-galactosamine-thiazoline (GalNGT) at resolutions from 1.84 to 2.7 Å. These structures showed N-acetylglucosamine and N-acetylgalactosamine to be recognized via identical sets of molecular interactions. Although the same sets of interaction were maintained with the gluco- and galacto-configured inhibitors, the inhibition constants suggested preferred recognition of the axial O4 when an aglycon moiety was present (Ki for PUGNAc > GalPUGNAc) but preferred recognition of an equatorial O4 when the aglycon was absent (Ki for GalNGT > NGT). Overall, this study reveals GH20C to be another tool that is unique in the arsenal of S. pneumoniae and that it may implement the effort of the bacterium to utilize and/or destroy the wide array of host glycans that it may encounter.
病原体肺炎链球菌(肺炎球菌)与其人类宿主之间相互作用的一个重要方面是这种细菌处理宿主聚糖的能力。为了实现宿主聚糖中糖苷键的裂解,肺炎链球菌部署了多种糖苷水解酶。在此,我们从肺炎链球菌中鉴定并表征了一种新的20家族糖苷水解酶GH20C。重组GH20C具有水解连接N-乙酰葡糖胺或N-乙酰半乳糖胺与多种糖苷配基残基的β-连接的能力,从而揭示该酶在体外是一种通用的N-乙酰己糖胺酶。测定了GH20C的无配体形式、与催化反应的N-乙酰葡糖胺和N-乙酰半乳糖胺产物形成的复合物以及与葡萄糖和半乳糖构型的抑制剂O-(2-乙酰氨基-2-脱氧-D-吡喃葡萄糖亚基)氨基N-苯基氨基甲酸酯(PUGNAc)、O-(2-乙酰氨基-2-脱氧-D-吡喃半乳糖亚基)氨基N-苯基氨基甲酸酯(GalPUGNAc)、N-乙酰-D-葡糖胺-噻唑啉(NGT)和N-乙酰-D-半乳糖胺-噻唑啉(GalNGT)形成的复合物的X射线晶体结构,分辨率在1.84至2.7 Å之间。这些结构表明,N-乙酰葡糖胺和N-乙酰半乳糖胺通过相同的分子相互作用集被识别。尽管与葡萄糖和半乳糖构型的抑制剂保持了相同的相互作用集,但抑制常数表明,当存在糖苷配基部分时,优先识别轴向O4(PUGNAc的Ki>GalPUGNAc),而当不存在糖苷配基时,优先识别赤道O4(GalNGT的Ki>NGT)。总体而言,这项研究揭示了GH20C是肺炎链球菌武器库中另一种独特的工具,它可能有助于该细菌利用和/或破坏它可能遇到的多种宿主聚糖。