https://www.ahs.ac.cn/images/0513-353X/images/top-banner1.jpg|#|苹果
https://www.ahs.ac.cn/images/0513-353X/images/top-banner2.jpg|#|甘蓝
https://www.ahs.ac.cn/images/0513-353X/images/top-banner3.jpg|#|菊花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner4.jpg|#|灵芝
https://www.ahs.ac.cn/images/0513-353X/images/top-banner5.jpg|#|桃
https://www.ahs.ac.cn/images/0513-353X/images/top-banner6.jpg|#|黄瓜
https://www.ahs.ac.cn/images/0513-353X/images/top-banner7.jpg|#|蝴蝶兰
https://www.ahs.ac.cn/images/0513-353X/images/top-banner8.jpg|#|樱桃
https://www.ahs.ac.cn/images/0513-353X/images/top-banner9.jpg|#|观赏荷花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner10.jpg|#|菊花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner11.jpg|#|月季
https://www.ahs.ac.cn/images/0513-353X/images/top-banner12.jpg|#|菊花

ACTA HORTICULTURAE SINICA ›› 2006, Vol. 33 ›› Issue (1): 122-124.

• 研究简报 • Previous Articles     Next Articles

Cloning and Prokaryotic Expression of Apple AFS Gene

  

  1. (1 Shandong Academy of Agricultural Sciences, Ji'nan 250100, China; 2College of Life Sciences, Shandong AgriculturalUniversity, Tai'an 271018, China)
  • Received:2005-01-17 Revised:2005-04-19 Online:2006-02-25 Published:2006-02-25

Abstract: α-farnesene synthase (AFS) gene from apple peel tissue was amplified by RT-PCR, and cloned into pET-30a ( + ) vector to construct recombinant prokaryotic exp ression vector pET-AFS. After transformation of E. coli and induced by 1 mmol/L isopropyl-β-D-thiogalactopyranoside ( IPTG) , recombinant protein with 66 kD was expressed in pET-AFS system and separated by SDS-PAGE electrophoresis. The maximum of protein was expressed when induced with IPTG for 6 h. The recombinant protein exp ressed as inclusion bodies.

Key words: Apple, α-farnesene, Prokaryotic expression, SDS-PAGE