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Enzymes Involved in the Biosynthesis of Arginine from Ornithine in Maritime Pine (

机译:从海洋松树中的鸟氨酸中参与生物合成的酶(

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摘要

The amino acids arginine and ornithine are the precursors of a wide range of nitrogenous compounds in all living organisms. The metabolic conversion of ornithine into arginine is catalyzed by the sequential activities of the enzymes ornithine transcarbamylase (OTC), argininosuccinate synthetase (ASSY) and argininosuccinate lyase (ASL). Because of their roles in the urea cycle, these enzymes have been purified and extensively studied in a variety of animal models. However, the available information about their molecular characteristics, kinetic and regulatory properties is relatively limited in plants. In conifers, arginine plays a crucial role as a main constituent of N-rich storage proteins in seeds and serves as the main source of nitrogen for the germinating embryo. In this work, recombinant PpOTC, PpASSY and PpASL enzymes from maritime pine (Pinus pinaster Ait.) were produced in Escherichia coli to enable study of their molecular and kinetics properties. The results reported here provide a molecular basis for the regulation of arginine and ornithine metabolism at the enzymatic level, suggesting that the reaction catalyzed by OTC is a regulatory target in the homeostasis of ornithine pools that can be either used for the biosynthesis of arginine in plastids or other nitrogenous compounds in the cytosol.
机译:氨基酸精氨酸和鸟氨酸是所有生物体中各种含氮化合物的前体。鸟氨酸转化为精氨酸的代谢转化通过酶鸟氨酸转基氨酰胺(OTC),精氨酸琥珀酸合成酶(ASSY)和精氨酸琥珀酸裂解酶(ASL)的顺序活性催化。由于尿素循环中的作用,这些酶已被纯化和广泛地研究了各种动物模型。然而,有关其分子特征,动力学和调节性质的可用信息在植物中相对有限。在针叶树中,精氨酸在种子中作为N-富含N的储存蛋白质的主要成分起到至关重要的作用,并用作发芽胚胎的氮的主要来源。在这项工作中,在大肠杆菌中产生来自海洋松(Pinus Pinaster Ait的重组PPOTC,PPASYY和PPASL酶,以实现其分子和动力学性质的研究。这里报道的结果为在酶促水平调节精氨酸和鸟氨酸代谢的结果提供了分子基础,表明OTC催化的反应是鸟氨酸池中的稳态中的调节靶标,这些靶标可用于塑性化的精氨酸生物合成或在细胞溶胶中的其他含氮化合物。

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