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Genomic characterization, molecular cloning and expression analysis of two terpene synthases from Thymus caespititius (Lamiaceae).
- Source :
-
Planta [Planta] 2013 Jul; Vol. 238 (1), pp. 191-204. Date of Electronic Publication: 2013 Apr 28. - Publication Year :
- 2013
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Abstract
- The identification, isolation and functional characterization of two genes encoding two monoterpene synthases-γ-terpinene synthase (Tctps2) and α-terpineol synthase (Tctps5)-from three chemically distinct Thymus caespititius (Lamiaceae) genotypes were performed. Genomic exon-intron structure was also determined for both terpene synthase genes, revealing an organization with seven exons and six introns. The cDNA of Tctps2 was 2,308 bp long and had an open reading frame of 1,794 bp encoding for a protein with 598 amino acids. Tctps5 was longer, mainly due to intron sequences, and presented high intraspecific variability on the plants analyzed. It encoded for a protein of 602 amino acids from an open reading frame of 1,806 bp comprising a total of 2,507 bp genomic sequence. The amino acid sequence of these two active Tctps genes shared 74 % pairwise identity, ranging between 42 and 94 % similarity with about 50 known terpene synthases of other Lamiaceae species. Gene expression revealed a multi-product Tctps2 and Tctps5 enzymes, producing γ-terpinene and α-terpineol as major components, respectively. These enzymatic results were consistent with the monoterpene profile present in T. caespititius field plants, suggesting a transcriptional regulation in leaves. Herewith reported for the first time for this species, these two newly characterized Tctps genes improve the understanding of the molecular mechanisms of reaction responsible for terpene biosynthesis and chemical diversity found in T. caespititius.
- Subjects :
- Alkyl and Aryl Transferases metabolism
Amino Acid Sequence
Base Sequence
Cloning, Molecular
Gene Expression Regulation, Plant
Introns
Lamiaceae metabolism
Molecular Sequence Data
Phylogeny
Plant Proteins genetics
Plant Proteins metabolism
Sequence Homology, Amino Acid
Alkyl and Aryl Transferases genetics
Lamiaceae enzymology
Lamiaceae genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1432-2048
- Volume :
- 238
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Planta
- Publication Type :
- Academic Journal
- Accession number :
- 23624978
- Full Text :
- https://doi.org/10.1007/s00425-013-1884-2