CSIR-Central Institute of Medicinal and Aromatic Plants (CSIR-CIMAP), Lucknow, Uttar Pradesh, India.
PLoS One. 2013 Sep 25;8(9):e74777. doi: 10.1371/journal.pone.0074777. eCollection 2013.
Withania somnifera is one of the most reputed medicinal plants of Indian systems of medicine synthesizing diverse types of secondary metabolites such as withanolides, alkaloids, withanamides etc. Present study comprises cloning and E. coli over-expression of a tropinone reductase gene (WsTR-I) from W. somnifera, and elucidation of biochemical characteristics and physiological role of tropinone reductase enzyme in tropane alkaloid biosynthesis in aerial tissues of the plant. The recombinant enzyme was demonstrated to catalyze NADPH-dependent tropinone to tropine conversion step in tropane metabolism, through TLC, GC and GC-MS-MS analyses of the reaction product. The functionally active homodimeric ~60 kDa enzyme catalyzed the reaction in reversible manner at optimum pH 6.7. Catalytic kinetics of the enzyme favoured its forward reaction (tropine formation). Comparative 3-D models of landscape of the enzyme active site contours and tropinone binding site were also developed. Tissue-wide and ontogenic stage-wise assessment of WsTR-I transcript levels revealed constitutive expression of the gene with relatively lower abundance in berries and young leaves. The tissue profiles of WsTR-I expression matched those of tropine levels. The data suggest that, in W. somnifera, aerial tissues as well possess tropane alkaloid biosynthetic competence. In vivo feeding of U-[(14)C]-sucrose to orphan shoot (twigs) and [(14)C]-chasing revealed substantial radiolabel incorporation in tropinone and tropine, confirming the de novo synthesizing ability of the aerial tissues. This inherent independent ability heralds a conceptual novelty in the backdrop of classical view that these tissues acquire the alkaloids through transportation from roots rather than synthesis. The TR-I gene expression was found to be up-regulated on exposure to signal molecules (methyl jasmonate and salicylic acid) and on mechanical injury. The enzyme's catalytic and structural properties as well as gene expression profiles are discussed with respect to their physiological overtones.
睡茄是印度传统医学中最受推崇的药用植物之一,它可以合成多种类型的次生代谢产物,如茄呢醇、生物碱、茄呢酰胺等。本研究包括从睡茄中克隆和大肠杆菌过表达托品酮还原酶基因(WsTR-I),并阐明该酶在植物地上组织中天麻碱生物合成中的生化特性和生理作用。通过 TLC、GC 和 GC-MS-MS 分析反应产物,证明重组酶能够催化 NADPH 依赖的托品酮向托品的转化步骤,从而完成托烷代谢。功能活性的同源二聚体~60 kDa 酶在最佳 pH 值 6.7 下以可逆方式催化该反应。酶的催化动力学有利于其正向反应(托品形成)。还对酶活性位点轮廓和托品酮结合位点的功能三维模型进行了比较。对 WsTR-I 转录本水平的组织广泛和个体发育阶段评估显示,该基因的表达是组成型的,在浆果和嫩叶中的丰度相对较低。WsTR-I 表达的组织谱与托品水平相匹配。数据表明,在睡茄中,地上组织也具有托烷生物碱生物合成能力。将 U-[(14)C]-蔗糖体内饲喂给孤枝(嫩枝)并进行 [(14)C]-追踪,发现托品酮和托品中有大量放射性标记物掺入,证实了地上组织具有从头合成能力。在经典观点认为这些组织通过从根部运输而不是合成获得生物碱的背景下,这种内在的独立能力预示着一个概念上的新颖性。TR-I 基因表达在暴露于信号分子(茉莉酸甲酯和水杨酸)和机械损伤时被上调。讨论了酶的催化和结构特性以及基因表达谱,以了解它们的生理内涵。