Molecular Cloning of a Partial Cadinane Synthase Gene from Artemisia annua

  • Song, Seung-hwan (Division of Applied Biology and Chemistry, College of Agriculture and Life Sciences, Seoul National University) ;
  • Chang, Yung-jin (Division of Applied Biology and Chemistry, College of Agriculture and Life Sciences, Seoul National University) ;
  • Kim, Jeong-gu (Division of Applied Biology and Chemistry, College of Agriculture and Life Sciences, Seoul National University) ;
  • Kim, Soo-Un (Division of Applied Biology and Chemistry, College of Agriculture and Life Sciences, Seoul National University)
  • Published : 1998.11.01

Abstract

Artemisia annua, an indigenous plant in Korea, contains a clinically important potent antimalarial principle, artemisinin. Artemisinin is a cadinane-type sesquiterpene endoperoxide. Cadinane synthase catalyzes the first committed step in artemisinin biosynthesis by cyclizing farnesyldiphosphate. In hopes of finding a cadinane synthase gene involved in artemisinin biosynthesis, oligonucleotides were synthesized on. the basis of the consensus nucleotide sequences and Nco I restriction sites for convenience in cloning. Specifically, nucleotide sequences of two highly conserved regions were deduced from the genes of similar function of Hyoscyamus muticus, Nicotiana tabacum, Abies grandis, Lycopersicon esculentum, and Gossypium hirsutum to construct a set of primers for polymerase chain reation (PCR). A 184 bp fragment was found to be amplified by PCR, and subsequently cloned. The gene revealed 62.8% identity in nucleotide and 55.6% in amino acid sequence to correspondent gene of N. tabacum. The gene was different from another sesquiterpene cyclase gene of A. annua, germacranadiene synthase gene, recently reported by Mercke and Bordelius (1998).

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