4.5 Article

Characterization and subcellular localization of geranylgeranyl diphosphate synthase from Catharanthus roseus

Journal

MOLECULAR BIOLOGY REPORTS
Volume 39, Issue 3, Pages 3235-3243

Publisher

SPRINGER
DOI: 10.1007/s11033-011-1091-9

Keywords

Geranylgeranyl diphosphate synthase; Isoprenoid; Chloroplast; Stromule; Catharanthus roseus

Funding

  1. Le STUDIUM (Agency for Research and Hosting Foreign associated Researchers in the Center region, France)
  2. Ministere de l'Enseignement Superieur et de la Recherche Scientifique (Tunisia)
  3. Ministere de l'Enseignement Superieur et de la Recherche (France)

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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.

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