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Purification of plastids from higher-plant roots

机译:从高等植物根系纯化质体

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A procedure is described for the purification of plastids from the roots ofPisum sativumL. The preparations obtained are appreciably free of contamination by other particles as judged by the distribution of organelle-specific marker enzymes and by electron microscopy. Latency of glutamate synthase (EC 2.6.1.53) within these preparations indicates that the plastids obtained are 90–95 intact, whilst the resistance of this enzyme, and glucose-6-phosphogluconate dehydrogenase (EC 1.1.1.43) to tryptic digestion in unlysed organelles indicates that they are at least 70–85 intact and may be suitable for studies of metabolite transp
机译:描述了从Pisum sativumL根部纯化质体的程序。根据细胞器特异性标记酶的分布和电子显微镜判断,所获得的制剂明显不受其他颗粒的污染。这些制剂中谷氨酸合酶 (EC 2.6.1.53) 的潜伏期表明获得的质体 90-95% 完整,而该酶和葡萄糖-6-磷酸葡萄糖酸脱氢酶 (EC 1.1.1.43) 对未裂解细胞器中胰蛋白酶消化的抗性表明它们至少 70-85% 完整,可能适用于代谢物反式的研究

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