- 4
- 0
- 约2.14万字
- 约 6页
- 2017-10-18 发布于河北
- 举报
抗草甘膦基因aroAM12及抗虫基因Bts1m的转基因棉株.pdf
31 1 Vol. 31, No. 1
2005 1 108~ 113 ACTA AGRONOMICA SINICA pp. 108- 113 Jan. , 2005
aroAM12 Bts1m
1 1,2 3 1,*
赵福永 谢龙旭 田颖川 徐培林
1 2 3
( , 510275; , 53002; ,
100080)
: pAM12-s1m, ( gene shuffling)
( aroAM12 ) Bt ( Bts1m) aroAM12 CaMV35S , Bts1m
2E-35S 8 , aroAM12 Bts1m
321 , aroAM12 , 52 PCR Southern blot
aroAM12 , 38 aroAM12 Bts1m Northern blotWestern blot
,
: ; ; aroAM12 ; Bts1m ;
: S562
Glyphosate-resistant and Bollworm-resistant Transgenic Cotton Plants with the
aroAM12 and Bts1m Genes
1 1, 2 3 1, *
ZHAO Fu-Yong , XIE Long-Xu ,TIAN Ying-Chuan , XU Pe-i Lin
1 2
( The Key Laboratory of Gene Engineering of Ministry of Education, Zhongshan University , Guang hou 510275, Guangdong ; College of Lfi e Science , Henan Nor-
3
mal University , Xinx iang 53002, Henan ; Institute of Microbiology , ChineseA cademy of Sciences, Beij ing 100080, China)
Abstract:A new binary vector, pAM12-s1m, harboring the aroAM12 gene encoding 5-enolpyruvyl-shikimate-3-phosphate
synthase ( EPSPS) and a synthetic recombinant Bts1m toxin gene consisting of 331N-terminal amino acids of CryIAc and
28 C-terminal amino acids of CryIAb was constructed1 The truncated aroAM12 gene, which was obtained through gene
shuffling technology, was ligated with a transit sequence of Arabidopsis EPSPS and expressed in cotton plants, and driven
by cauliflower mosaic virus 35S ( CaMV35S) promoter1 T
原创力文档

文档评论(0)