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

Applying the genomic library construction strategy and colony screening, a new aro A 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 in...

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Veröffentlicht in:Molecular biology reports 2012-12, Vol.39 (12), p.10939-10947
Hauptverfasser: Zhou, Chang-Yan, Tian, Yong-Sheng, Xu, Zhi-Sheng, Zhao, Wei, Chen, Chen, Bao, Wen-Hua, Bian, Lin, Cai, Run, Wu, Ai-Zhong
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Sprache:eng
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Zusammenfassung:Applying the genomic library construction strategy and colony screening, a new aro A 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.
ISSN:0301-4851
1573-4978
DOI:10.1007/s11033-012-1994-0