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ACTA HORTICULTURAE SINICA ›› 2016, Vol. 43 ›› Issue (2): 356-364.doi: 10.16420/j.issn.0513-353x.2015-0803

• Research Notes • Previous Articles     Next Articles

Cloning and Expression Analysis of Terpene Synthase Gene from Jasminum sambac

YU Ying1,*,CHEN Dan1,*,SUN Jun2,Lü Shi-heng1,CHEN Gui-xin1,**,and YE Nai-xing1,**   

  1. 1College of Horticulture,Fujian Agriculture and Forestry University,Key Laboratory of Tea Science at Universities in Fujian,Fuzhou 350002,China;2Tea Research Institute,Fujian Academy of Agricultural Sciences,Fu’an,Fujian 355015,China
  • Online:2016-02-25 Published:2016-02-25

Abstract: The full length cDNA of terpene synthase gene(JsTPS)was cloned by combination of RT-PCR and RACE from petals of Jasminum sambac. The results showed that full length cDNA contained 1 491 bp including an 1 884 bp ORF,encoding a 56 989.7 D protein with 496 amino acids whose molecular weight was consistent to that of product of the gene by prokaryotic expression;The result of alignment of amino acid showed that the gene had a homology of 75% to that of olive(Olea europaea),belonging to α-Farnesene synthases;Quantities of the gene were detected by real-time PCR in process of opening of flower,the results showed that the expressing level of the gene was minimum at 18:00 when the flowers were not open,then had been increasing until at 22:00 when the expressing level reached to maximum and the flowers was opening.

Key words: Jasminum sambac, terpene synthase gene, quantitative real-time PCR, prokaryotic expression

CLC Number: