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长春花香叶基二磷酸合酶的表征和亚细胞定位。

Characterization and subcellular localization of geranylgeranyl diphosphate synthase from Catharanthus roseus.

机构信息

EA2106, Biomolécules et Biotechnologies Végétales, Université François-Rabelais, 31 avenue Monge, 37200 Tours, France.

出版信息

Mol Biol Rep. 2012 Mar;39(3):3235-43. doi: 10.1007/s11033-011-1091-9. Epub 2011 Jun 25.

Abstract

The enzyme geranylgeranyl diphosphate synthase (GGPS: EC 2.5.1.1, EC 2.5.1.10, EC 2.5.1.29) catalyses the formation of geranylgeranyl diphosphate (GGPP) from isopentenyl diphosphate and dimethylallyl diphosphate via three successive condensation reactions. A full-length nucleotide sequence of GGPS (named CrGGPS) was cloned from the medicinal plant Catharanthus roseus. The deduced polypeptide has 383 amino acids with a calculated mass of 41.6 kDa and possesses prenyltransferase signatures characteristic of plant type II GGPS. The enzyme was characterized by functional complementation in carotenoid accumulating strains of Escherichia coli. When cultures of Catharanthus cell lines were treated with methyljasmonate, no specific increase in transcript levels were observed. In plants, GGPS are encoded by a small multigene family and the isoforms have been shown to be localized in three different subcellular compartments: chloroplast, endoplasmic reticulum and mitochondria. We investigated the subcellular distribution of CrGGPS through transient transformations of C. roseus cells with a yellow fluorescent protein-fused construct. Our results clearly indicate that CrGGPS is located to plastids within stroma and stromules.

摘要

香叶基香叶基二磷酸合酶(GGPS:EC 2.5.1.1、EC 2.5.1.10、EC 2.5.1.29)催化异戊烯二磷酸和二甲基烯丙基二磷酸通过三个连续的缩合反应形成香叶基香叶基二磷酸(GGPP)。从药用植物长春花中克隆了全长核苷酸序列 GGPs(命名为 CrGGPS)。推导出的多肽具有 383 个氨基酸,计算质量为 41.6 kDa,具有植物 II 型 GGPs 的特征性 prenyltransferase 特征。该酶通过在积累类胡萝卜素的大肠杆菌菌株中的功能互补进行了表征。当长春花细胞系的培养物用茉莉酸甲酯处理时,未观察到转录水平的特异性增加。在植物中,GGPS 由一个小的多基因家族编码,同工型已被证明定位于三个不同的亚细胞隔室:叶绿体、内质网和线粒体。我们通过用黄色荧光蛋白融合构建体瞬时转化长春花细胞来研究 CrGGPS 的亚细胞分布。我们的结果清楚地表明,CrGGPS 位于质体的基质和 stromules 中。

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