Department of Chemistry, The University of North Carolina at Chapel Hill, North Carolina, 27599, United States.
Department of Chemistry, The University of North Carolina at Chapel Hill, North Carolina, 27599, United States; Department of Microbiology and Immunology, The University of North Carolina at Chapel Hill, North Carolina, 27599, United States.
Protein Expr Purif. 2023 Oct;210:106326. doi: 10.1016/j.pep.2023.106326. Epub 2023 Jun 20.
Polyamines play essential roles in plant growth and survival. Arginine decarboxylase (ADC), which converts arginine to agmatine, catalyzes the first step in polyamine biosynthesis from arginine. However, few biochemical studies with purified plant ADCs have been conducted to evaluate their catalytic efficiency. Tomato genome encodes two arginine decarboxylases: SlADC1 and SlADC2, which are critical for growth, development, and immune responses against bacterial pathogens. We expressed and purified soluble SlADC1 as a recombinant protein fused with maltose-binding protein tag from E. coli Rosetta 2(DE3) cells. Using the purified fusion protein, we characterized the biochemical properties of SlADC1 in vitro and explored it as a target of the bacterial small molecule phevamine A. We confirmed that the activity of SlADC1 depends on the cofactor pyridoxal 5'-phosphate. SlADC1 is specific toward l-arginine and its kinetic parameters were measured using a liquid chromatography-mass spectrometry method. Phevamine A is a competitive inhibitor of SlADC1 and reduces the activity of SlADC1 at high micromolar concentrations. Our purification and biochemical characterization of SlADC1 sets the stage for inhibition studies of this enzyme.
多胺在植物的生长和存活中起着至关重要的作用。精氨酸脱羧酶(ADC)将精氨酸转化为胍丁胺,催化多胺生物合成从精氨酸开始的第一步。然而,很少有关于纯化植物 ADC 的生化研究来评估它们的催化效率。番茄基因组编码两种精氨酸脱羧酶:SlADC1 和 SlADC2,它们对生长、发育和对细菌病原体的免疫反应至关重要。我们从大肠杆菌 Rosetta 2(DE3)细胞中表达并纯化了可溶的 SlADC1,它与麦芽糖结合蛋白标签融合。使用纯化的融合蛋白,我们在体外表征了 SlADC1 的生化特性,并探索了它作为细菌小分子 phevaamine A 的靶标。我们证实 SlADC1 的活性依赖于辅因子吡哆醛 5'-磷酸。SlADC1 对 l-精氨酸具有特异性,并使用液相色谱-质谱法测量了其动力学参数。Phevaamine A 是 SlADC1 的竞争性抑制剂,在高微摩尔浓度下降低 SlADC1 的活性。我们对 SlADC1 的纯化和生化特性的研究为该酶的抑制研究奠定了基础。