Department of NanoBiotechnology, ViennaInstitute of BioTechnology, Universität für Bodenkultur Wien, A-1190 Vienna,Austria.
Glycobiology. 2010 Jun;20(6):787-98. doi: 10.1093/glycob/cwq035. Epub 2010 Mar 3.
Glycosylation is a frequent and heterogeneous posttranslational protein modification occurring in all domains of life. While protein N-glycosylation at asparagine and O-glycosylation at serine, threonine or hydroxyproline residues have been studied in great detail, only few data are available on O-glycosidic attachment of glycans to the amino acid tyrosine. In this study, we describe the identification and characterization of a bacterial protein tyrosine O-glycosylation system. In the Gram-positive, mesophilic bacterium Paenibacillus alvei CCM 2051(T), a polysaccharide consisting of [-->3)-beta-d-Galp-(1[alpha-d-Glcp-(1-->6)] -->4)-beta-d-ManpNAc-(1-->] repeating units is O-glycosidically linked via an adaptor with the structure -[GroA-2-->OPO(2)-->4-beta-d-ManpNAc-(1-->4)] -->3)-alpha-l-Rhap-(1-->3)-alpha-l-Rhap-(1-->3)-alpha-l-Rhap-(1-->3)-beta-d-Galp-(1--> to specific tyrosine residues of the S-layer protein SpaA. A +AH4-24.3-kb S-layer glycosylation (slg) gene cluster encodes the information necessary for the biosynthesis of this glycan chain within 18 open reading frames (ORF). The corresponding translation products are involved in the biosynthesis of nucleotide-activated monosaccharides, assembly and export as well as in the transfer of the completed polysaccharide chain to the S-layer target protein. All ORFs of the cluster, except those encoding the nucleotide sugar biosynthesis enzymes and the ATP binding cassette (ABC) transporter integral transmembrane proteins, were disrupted by the insertion of the mobile group II intron Ll.LtrB, and S-layer glycoproteins produced in mutant backgrounds were analyzed by mass spectrometry. There is evidence that the glycan chain is synthesized in a process comparable to the ABC-transporter-dependent pathway of the lipopolysaccharide O-polysaccharide biosynthesis. Furthermore, with the protein WsfB, we have identified an O-oligosaccharyl:protein transferase required for the formation of the covalent beta-d-Gal-->Tyr linkage between the glycan chain and the S-layer protein.
糖基化是一种常见的、不均一的翻译后蛋白质修饰,发生在所有生命领域。尽管天冬酰胺的蛋白质 N-糖基化和丝氨酸、苏氨酸或羟脯氨酸残基的 O-糖基化已经得到了深入研究,但关于糖链与氨基酸酪氨酸的 O-糖苷键连接的信息却很少。在这项研究中,我们描述了一种细菌蛋白酪氨酸 O-糖基化系统的鉴定和特征。在革兰氏阳性、嗜温细菌 Paenibacillus alvei CCM 2051(T)中,一种由 [-->3)-β-d-Galp-(1[alpha-d-Glcp-(1-->6)] -->4)-β-d-ManpNAc-(1-->] 重复单元组成的多糖通过一个接头与 S-层蛋白 SpaA 上特定的酪氨酸残基发生 O-糖苷键连接,接头的结构为 -[GroA-2-->OPO(2)-->4-β-d-ManpNAc-(1-->4)] -->3)-α-l-Rhap-(1-->3)-α-l-Rhap-(1-->3)-α-l-Rhap-(1-->3)-β-d-Galp-(1-->。一个 +AH4-24.3-kb S-层糖基化 (slg) 基因簇在 18 个开放阅读框 (ORF) 中编码了合成这种糖链的信息。相应的翻译产物参与核苷酸激活单糖的生物合成、组装和输出,以及将完成的多糖链转移到 S-层靶蛋白。除了编码核苷酸糖生物合成酶和 ATP 结合盒 (ABC) 转运蛋白整合跨膜蛋白的 ORF 外,该基因簇的所有 ORF 都被移动的组 II 内含子 Ll.LtrB 插入破坏,并且在突变背景下产生的 S-层糖蛋白通过质谱分析。有证据表明,糖链的合成过程类似于脂多糖 O-多糖生物合成的 ABC 转运蛋白依赖性途径。此外,我们还发现了一种 WsfB 蛋白,它是一种 O-寡糖基转移酶,负责形成糖链与 S-层蛋白之间的共价β-d-Gal-->Tyr 键。