Yurist-Doutsch Sophie, Eichler Jerry
Dept. of Life Sciences, Ben Gurion University, P.O. Box 653, Beersheva 84105, Israel.
J Bacteriol. 2009 May;191(9):3068-75. doi: 10.1128/JB.01838-08. Epub 2009 Feb 27.
While Eukarya, Bacteria, and Archaea are all capable of protein N glycosylation, the archaeal version of this posttranslational modification is the least understood. To redress this imbalance, recent studies of the halophilic archaeon Haloferax volcanii have identified a gene cluster encoding the Agl proteins involved in the assembly and attachment of a pentasaccharide to select Asn residues of the surface layer glycoprotein in this species. However, because the automated tools used for rapid annotation of genome sequences, including that of H. volcanii, are not always accurate, a reannotation of the agl cluster was undertaken in order to discover genes not previously recognized. In the present report, reanalysis of the gene cluster that includes aglB, aglE, aglF, aglG, aglI, and aglJ, which are known components of the H. volcanii protein N-glycosylation machinery, was undertaken. Using computer-based tools or visual inspection, together with transcriptional analysis and protein expression approaches, genes encoding AglP, AglQ, and AglR are now described.
虽然真核生物、细菌和古菌都能够进行蛋白质N-糖基化,但这种翻译后修饰的古菌形式是了解最少的。为了纠正这种不平衡,最近对嗜盐古菌沃氏嗜盐菌的研究确定了一个基因簇,该基因簇编码参与将五糖组装并连接到该物种表层糖蛋白特定天冬酰胺残基上的Agl蛋白。然而,由于用于快速注释基因组序列(包括沃氏嗜盐菌的基因组序列)的自动化工具并不总是准确的,因此对agl基因簇进行了重新注释,以发现以前未被识别的基因。在本报告中,对包括aglB、aglE、aglF、aglG、aglI和aglJ的基因簇进行了重新分析,这些基因是沃氏嗜盐菌蛋白质N-糖基化机制的已知组成部分。通过基于计算机的工具或目视检查,结合转录分析和蛋白质表达方法,现在描述了编码AglP、AglQ和AglR的基因。