African Journal of
Biotechnology

  • Abbreviation: Afr. J. Biotechnol.
  • Language: English
  • ISSN: 1684-5315
  • DOI: 10.5897/AJB
  • Start Year: 2002
  • Published Articles: 12487

Full Length Research Paper

The 1-hydroxy-2-methyl-butenyl 4-diphosphate reductase gene from Taxus media: Cloning, characterization and functional identification

Yiming Sun1, Min Chen2, Jun Tang1, Wanhong Liu1, 3, Chunxian Yang1, Yijian Yang1, Xiaozhong Lan4, Minghsiun Hsieh5 and Zhihua Liao1*
1Laboratory of Natural Products and Metabolic Engineering, Chongqing Sweet potato Research Center, Key Laboratory of Eco-environments in Three Gorges Reservoir Region (Ministry of Education), School of Life Sciences, Southwest University, Chongqing 400715, People’s Republic of China. 2College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, People’s Republic of China. 3Department of Biology, Chongqing University of Science and technology, Chongqing 400042, People’s Republic of China. 4Agricultural and Animal Husbandry College, Tibet University, Linzhi of Tibet 860000, People’s Republic of China. 5Institute of Plant and Microbial Biology, Academia Sinica, Taipei 11529, Taiwan.  
Email: [email protected] or [email protected]

  •  Accepted: 24 July 2009
  •  Published: 15 September 2009

Abstract

1-Hydroxy-2-methyl-butenyl 4-diphosphate reductase (HDR:EC: 1.17.1.2) is the last and key enzyme involved in the 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway, which provides the general precursors for taxol biosynthesis and is the important candidate gene for metabolic engineering of the taxol biosynthetic pathway. The gene encoding HDR from Taxus media (designated as TmHDR; GenBank accession number: EF541129) was cloned using RACE, characterized at the levels of bioinformatics and tissue expression pattern, and finally functionally identified with the genetic complementation. The full-length cDNA of TmHDR was 1987 bp containing an 1425-bp open reading frame (ORF) that encoded a polypeptide of 474 amino acids with a calculated molecular mass of 53.2 kDa and an isoelectric point of 5.65. Comparative and bioinformatic analysis revealed that TmHDR showed extensive homology with HDRs from other plant species. The subcellular prediction showed that TmHDR owned a plastidial transit peptide of 47 amino acids at its N terminus, which directed TmHDR to plastid. The phylogenetic analysis revealed that TmHDR belonged to gymnosperm HDRs. The tissue expression pattern analysis indicated that TmHDR expressed in all tested tissues including cortices, stems, roots and leaves but at different levels. The highest expression level of TmHDR was found in leaves, followed by roots and cortices; and the expression of TmHDR was very low in stems. Finally, TmHDR was functionally expressed in lethal Ecoli HDR mutant and could rescue the mutants. So, the genetic complementation assay demonstrated that TmHDR did encode the protein that had the typical activity of HDR proteins. In summary, the present study will be helpful to understand more about the role of HDR involved in the Taxol biosynthesis at the molecular level and provides an important candidate gene for metabolic engineering of the taxol biosynthesis in Taxus species plants.

 

Key words: 1-hydroxy-2-methyl-butenyl 4-diphosphate reductase (HDR), cloning, genetic complementation, Taxus media, tissue expression.