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AglB催化古菌N-糖基化过程中的寡糖基转移酶步骤,在嗜热嗜酸泉古菌嗜酸热硫化叶菌中至关重要。

AglB, catalyzing the oligosaccharyl transferase step of the archaeal N-glycosylation process, is essential in the thermoacidophilic crenarchaeon Sulfolobus acidocaldarius.

作者信息

Meyer Benjamin H, Albers Sonja-Verena

机构信息

Molecular Biology of Archaea, Max-Planck Institute for terrestrial Microbiology, Karl-von-Frisch-Strasse 10, 35043, Marburg.

出版信息

Microbiologyopen. 2014 Aug;3(4):531-43. doi: 10.1002/mbo3.185. Epub 2014 Jun 10.

Abstract

Sulfolobus acidocaldarius, a thermo-acidophilic crenarchaeon which grows optimally at 76 °C and pH 3, exhibits an astonishing high number of N-glycans linked to the surface (S-) layer proteins. The S-layer proteins as well as other surface-exposed proteins are modified via N-glycosylation, in which the oligosaccharyl transferase AglB catalyzes the final step of the transfer of the glycan tree to the nascent protein. In this study, we demonstrated that AglB is essential for the viability of S. acidocaldarius. Different deletion approaches, that is, markerless in-frame deletion as well as a marker insertion were unsuccessful to create an aglB deletion mutant. Only the integration of a second aglB gene copy allowed the successful deletion of the original aglB.

摘要

嗜酸热硫化叶菌是一种嗜热嗜酸的泉古菌,在76°C和pH 3的条件下生长最佳,其表面(S-)层蛋白上连接有数量惊人的N-聚糖。S层蛋白以及其他表面暴露蛋白通过N-糖基化进行修饰,其中寡糖基转移酶AglB催化聚糖树转移到新生蛋白的最后一步。在本研究中,我们证明AglB对嗜酸热硫化叶菌的生存能力至关重要。不同的缺失方法,即无标记框内缺失以及标记插入,均未能成功构建aglB缺失突变体。只有整合第二个aglB基因拷贝才能成功删除原始的aglB。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9a9/4287180/e7b4d6dc8b52/mbo30003-0531-f1.jpg

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