Identification of a new gene encoding 5-enolpyruvylshikimate-3-phosphate synthase using genomic library construction strategy

被引:9
|
作者
Zhou, Chang-Yan [1 ,2 ]
Tian, Yong-Sheng [3 ]
Xu, Zhi-Sheng [3 ]
Zhao, Wei [3 ]
Chen, Chen [3 ]
Bao, Wen-Hua [3 ]
Bian, Lin [3 ]
Cai, Run [1 ]
Wu, Ai-Zhong [1 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Coll Agr & Biol, Shanghai 200240, Peoples R China
[2] Shanghai Acad Agr Sci, Inst Agrifood Stand & Testing Technol, Shanghai 201403, Peoples R China
[3] Shanghai Acad Agr Sci, Shanghai Key Lab Agr Genet & Breeding, Biotechnol Res Inst, Shanghai 201106, Peoples R China
关键词
EPSPS; Pseudomonas fluorescens; Enzyme kinetic values; Genomic library; 3-PHOSPHATE SYNTHASE; 5-ENOPYRUVYLSHIKIMATE-3-PHOSPHATE SYNTHASE; ESCHERICHIA-COLI; HERBICIDE GLYPHOSATE; CATALYTIC RESIDUES; SHIKIMATE PATHWAY; HIGH TOLERANCE; AROA; RESISTANCE; SUBSTITUTION;
D O I
10.1007/s11033-012-1994-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Applying the genomic library construction strategy and colony screening, a new aroA gene encoding 5-enolpyruvylshikimate-3-phosphate synthase has been identified, cloned and overexpressed in Escherichia coli, and the enzyme was purified to homogeneity. Kinetic analysis of the AroA (P.fluorescens) indicated that the full-length enzyme exhibits 10-fold increased IC50 and an approximately 38-fold increased K (i) for glyphosate compared to those of the AroA (E.coli) , while retaining high affinity for the substrate phosphoenolpyruvate. Furthermore, we have transformed the new aroA (P.fluorescens) gene into Arabidopsis thaliana via a floral dip method, and demonstrated that transgenic A. thaliana plants exhibit significant glyphosate resistance when compared with the wild type.
引用
收藏
页码:10939 / 10947
页数:9
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