豌豆叶中的谷胱甘肽还原酶:对非生物胁迫的反应和过氧异构体同工酶的特征。

María C Romero-Puertas, Francisco J Corpas, Luisa M Sandalio, Marina Leterrier, María Rodríguez-Serrano, Luis A Del Río, José M Palma
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引用次数: 0

摘要

首次纯化了存在于过氧物酶体中的谷胱甘肽还原酶(GR;EC 1.6.4.2)同工酶,并通过免疫金电子显微镜报告了它在这些细胞器中的明确定位。该酶纯化了约 21 倍,比活度为 9523 单位毫克(-1)蛋白质,产量为 44 微克蛋白质千克(-1)叶片。过氧化物酶体 GR 的亚单位大小为 56 kDa,等电点为 5.4。针对豌豆(Pisum sativum)叶片总 GR 的多克隆抗体可识别该酶。GR在过氧物酶体中的定位增加了叶绿体和线粒体中GR同工酶的含量,这表明在植物生长条件下,根据各细胞器的新陈代谢情况,该酶有多种不同的细胞区系定位。研究人员调查了不同胁迫条件下 GR 在豌豆植物多个器官中的表达水平。讨论了过氧物酶体 GR 在镉毒性、强光、黑暗、高温、受伤和低温等非生物胁迫条件下可能发挥的作用。
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Glutathione reductase from pea leaves: response to abiotic stress and characterization of the peroxisomal isozyme.

The glutathione reductase (GR; EC 1.6.4.2) isozyme present in peroxisomes has been purified for the first time, and its unequivocal localization in these organelles, by immunogold electron microscopy, is reported. The enzyme was purified c. 21-fold with a specific activity of 9523 units mg(-1) protein, and a yield of 44 microg protein kg(-1) leaves was obtained. The subunit size of the peroxisomal GR was 56 kDa and the isoelectric point was 5.4. The enzyme was recognized by a polyclonal antibody raised against total GR from pea (Pisum sativum) leaves. The localization of GR in peroxisomes adds to chloroplasts and mitochondria where GR isozymes are also present, and suggests a multiple targeting of this enzyme to distinct cell compartments depending on the metabolism of each organelle under the plant growth conditions. The expression level of GR in several organs of pea plants and under different stress conditions was investigated. The possible role of peroxisomal GR under abiotic stress conditions, such as cadmium toxicity, high light, darkness, high temperature, wounding and low temperature, is discussed.

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