Morinaka Brandon I, Vagstad Anna L, Piel Jörn
Institute of Microbiology, Eidgenössische Technische Hochschule (ETH) Zurich, Zurich, Switzerland; Department of Pharmacy, National University of Singapore, Singapore, Singapore.
Institute of Microbiology, Eidgenössische Technische Hochschule (ETH) Zurich, Zurich, Switzerland.
Methods Enzymol. 2018;604:237-257. doi: 10.1016/bs.mie.2018.01.033. Epub 2018 Apr 11.
The identification of the polytheonamide (poy) gene cluster led to the discovery of the enzyme PoyD, a member of the radical S-adenosylmethionine superfamily capable of introducing d-amino acids into a ribosomally synthesized peptide. This enzyme was used as a starting point to identify additional radical S-adenosylmethionine peptide epimerases in other cyanobacterial genomes, which show different epimerization patterns compared to PoyD. During the course of studying these enzymes by heterologous expression in Escherichia coli, we developed a two-step strategy to (1) detect epimerase activity and (2) localize where epimerization occurs based on an in vivo deuterium labeling strategy. The procedures for these two methods are described in the following chapter and will set the stage for further study of these enzymes.
聚醚酰胺(poy)基因簇的鉴定促使人们发现了酶PoyD,它是自由基S-腺苷甲硫氨酸超家族的成员,能够将d-氨基酸引入核糖体合成的肽中。该酶被用作起点,以鉴定其他蓝藻基因组中额外的自由基S-腺苷甲硫氨酸肽差向异构酶,这些酶与PoyD相比显示出不同的差向异构化模式。在通过在大肠杆菌中进行异源表达来研究这些酶的过程中,我们开发了一种两步策略,即(1)检测差向异构酶活性,以及(2)基于体内氘标记策略确定差向异构化发生的位置。以下章节将描述这两种方法的步骤,它们将为进一步研究这些酶奠定基础。