Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractComparison of transcripts in Phalaenopsis bellina and Phalaenopsis equestris (Orchidaceae) flowers to deduce monoterpene biosynthesis pathway    Next AbstractAdsorption energy distribution model for VOCs onto activated carbons »

Plant J


Title:A novel homodimeric geranyl diphosphate synthase from the orchid Phalaenopsis bellina lacking a DD(X)2-4D motif
Author(s):Hsiao YY; Jeng MF; Tsai WC; Chuang YC; Li CY; Wu TS; Kuoh CS; Chen WH; Chen HH;
Address:"Department of Life Sciences, National Cheng Kung University, Tainan 701, Taiwan"
Journal Title:Plant J
Year:2008
Volume:20080509
Issue:5
Page Number:719 - 733
DOI: 10.1111/j.1365-313X.2008.03547.x
ISSN/ISBN:1365-313X (Electronic) 0960-7412 (Linking)
Abstract:"Geranyl diphosphate (GDP) is the precursor of monoterpenes, which are the major floral scent compounds in Phalaenopsis bellina. The cDNA of P. bellina GDP synthase (PbGDPS) was cloned, and its sequence corresponds to the second Asp-rich motif (SARM), but not to any aspartate-rich (Asp-rich) motif. The recombinant PbGDPS enzyme exhibits dual prenyltransferase activity, producing both GDP and farnesyl diphosphate (FDP), and a yeast two-hybrid assay and gel filtration revealed that PbGDPS was able to form a homodimer. Spatial and temporal expression analyses showed that the expression of PbGDPS was flower specific, and that maximal PbGDPS expression was concomitant with maximal emission of monoterpenes on day 5 post-anthesis. Homology modelling of PbGDPS indicated that the Glu-rich motif might provide a binding site for Mg(2+) and catalyze the formation of prenyl products in a similar way to SARM. Replacement of the key Glu residues with alanine totally abolished enzyme activity, whereas their mutation to Asp resulted in a mutant with two-thirds of the activity of the wild-type protein. Phylogenetic analysis indicated that plant GDPS proteins formed four clades: members of both GDPS-a and GDPS-b clades contain Asp-rich motifs, and function as homodimers. In contrast, proteins in the GDPS-c and GDPS-d clades do not contain Asp-rich motifs, but although members of the GDPS-c clade function as heterodimers, PbGDPS, which is more closely related to the GDPS-c clade proteins than to GDPS-a and GDPS-b proteins, and is currently the sole member of the GDPS-d clade, functions as a homodimer"
Keywords:"Amino Acid Sequence Cloning, Molecular DNA, Complementary/genetics DNA, Plant/genetics Dimethylallyltranstransferase/*genetics Flowers/enzymology/genetics Gene Expression Genes, Plant Models, Molecular Molecular Sequence Data Monoterpenes/metabolism Mutag;"
Notes:"MedlineHsiao, Yu-Yun Jeng, Mei-Fen Tsai, Wen-Chieh Chuang, Yu-Chen Li, Chia-Ying Wu, Tian-Shung Kuoh, Chang-Sheng Chen, Wen-Huei Chen, Hong-Hwa eng Research Support, Non-U.S. Gov't England 2008/05/10 Plant J. 2008 Sep; 55(5):719-33. doi: 10.1111/j.1365-313X.2008.03547.x. Epub 2008 May 9"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 26-12-2024