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ACTA HORTICULTURAE SINICA ›› 2010, Vol. 37 ›› Issue (7): 1132-1138.

• 观赏植物 • Previous Articles     Next Articles

Cloning and Recombinant Protein Expression of ACC Synthase Genes in Cut Roses(Rosa hybrida)

TAN Yuan-jun1,XUE Jing-qi2,TONG Zheng1,MA Nan1,and GAO Jun-ping1,*

  

  1. (1Department of Ornamental Horticulture and Landscape Architecture,China Agricultural University,Beijing 100193,China;2Institute of Vegetables and Flowers,Chinese Academy of Agricultural Sciences,Beijing 100081,China)
  • Received:2010-06-15 Revised:2010-06-22 Online:2010-07-25 Published:2010-07-25
  • Contact: GAO Jun-ping

Abstract: Our previous work showed that the expression of ACC synthase genes was contributed to the effects of ethylene on hastening flower opening. In the present work,we isolated the wound-inducible and ethylene up-regulated ACS genes,namely Rh-ACS1 and Rh-ACS3,from cut rose petals. The full length of Rh-ACS1 is 2 132 bp,contains a 1 476 bp ORF which encodes a putative ACS protein with 491 aa,while the entire Rh-ACS3 is 1 734 bp in length,and contains a 1 545 bp ORF which encodes a putative ACS protein with 514 aa. The ORFs of Rh-ACS1 and Rh-ACS3 were inserted into pGEX-4T-1 and pET-30a to express the recombinant proteins in E.coli,respectively. The expression of predicted 70 kD and 60 kD recombinant proteins were induced by isopropyl β-D-thiogalacto-pyranoside(IPTG)at a final concentration of 0.6 mmol · L-1 for 3 h at 37 ℃.

Key words: cut rose, ACS, gene cloning, procaryotic expression

CLC Number: