Shoji Tsubasa
Graduate School of Biological Sciences, Nara Institute of Science and Technology, Takayama, 8916-5, Ikoma, Japan.
Methods Mol Biol. 2018;1694:215-223. doi: 10.1007/978-1-4939-7398-9_20.
The intracellular localization of enzymes provides key information for understanding complex metabolic pathways. Based on enzyme localization data, the involvement of multiple organelles and the movement of metabolites between cellular compartments have been suggested for a number of pathways. Transient expression of fluorescently tagged proteins in the leaves of Nicotiana benthamiana through Agrobacterium infiltration is a simple and versatile way to examine the intracellular localization of proteins of interest. Here, this method was applied to demonstrate the peroxisomal localization of a pair of homologous copper-containing amine oxidases (CuAOs) from tobacco with distinct substrate preferences: diamine oxidase (DAO), which mediates polyamine catabolism, and N-methylputrescine oxidase (MPO), which is involved in nicotine biosynthesis. Our results demonstrate that the Agrobacterium infiltration protocol can be effectively used to study the intracellular localization of oxidases that localize to the peroxisome.
酶的细胞内定位为理解复杂的代谢途径提供了关键信息。基于酶定位数据,对于许多途径而言,已表明多种细胞器参与其中以及代谢物在细胞区室之间的移动。通过农杆菌浸润在本氏烟草叶片中瞬时表达荧光标记蛋白,是一种用于检测感兴趣蛋白细胞内定位的简单且通用的方法。在此,该方法被用于证明来自烟草的一对具有不同底物偏好的同源含铜胺氧化酶(CuAO)的过氧化物酶体定位:介导多胺分解代谢的二胺氧化酶(DAO)和参与尼古丁生物合成的N-甲基腐胺氧化酶(MPO)。我们的结果表明,农杆菌浸润方案可有效地用于研究定位于过氧化物酶体的氧化酶的细胞内定位。