Zmuda Anthony J, Niehaus Thomas D
Department of Plant and Microbial Biology, University of Minnesota, St. Paul, MN, United States.
Department of Plant and Microbial Biology, University of Minnesota, St. Paul, MN, United States.
Methods Enzymol. 2023;680:3-34. doi: 10.1016/bs.mie.2022.08.002. Epub 2022 Sep 2.
At least a quarter of the protein-encoding genes in plant genomes are predicted to encode enzymes for which no physiological function is known. Determining functions for these uncharacterized enzymes is key to understanding plant metabolism. Functional characterization typically requires expression and purification of recombinant enzymes to be used in enzyme assays and/or for protein structure elucidation studies. Here, we describe several practical considerations used to improve the heterologous expression and purification of Arabidopsis thaliana and Zea mays NAD(P)HX dehydratase (NAXD) and NAD(P)HX epimerase (NAXE), two enzymes that are involved in repair of chemically damaged NAD(P)H cofactors. We provide protocols for transit peptide prediction and construct design, expression in Escherichia coli, and purification of NAXD and NAXE. Many of these strategies are generally applicable to the purification of any plant protein.
据预测,植物基因组中至少四分之一的蛋白质编码基因所编码的酶尚无已知的生理功能。确定这些未表征酶的功能是理解植物代谢的关键。功能表征通常需要表达和纯化重组酶,以便用于酶活性测定和/或蛋白质结构解析研究。在此,我们描述了几个实际考量因素,用于改进拟南芥和玉米的NAD(P)HX脱水酶(NAXD)和NAD(P)HX差向异构酶(NAXE)的异源表达和纯化,这两种酶参与化学损伤的NAD(P)H辅因子的修复。我们提供了转运肽预测和构建体设计、在大肠杆菌中的表达以及NAXD和NAXE纯化的方案。这些策略中的许多通常适用于任何植物蛋白的纯化。