Characterization of a Glyphosate-Tolerant Enzyme from Streptomyces svecius: A Distinct Class of 5-Enolpyruvylshikimate-3-phosphate Synthases

被引:12
作者
Griffin, Samantha L. [1 ]
Chekan, Jonathan R. [2 ,3 ]
Lira, Justin M. [1 ]
Robinson, Andrew E. [1 ]
Yerkes, Carla N. [1 ]
Siehl, Daniel L. [1 ]
Wright, Terry R. [1 ]
Nair, Satish K. [2 ]
Cicchillo, Robert M. [1 ]
机构
[1] Corteva Agrisci, Indianapolis, IN 46268 USA
[2] Univ Illinois, Dept Biochem, Urbana, IL 61801 USA
[3] Univ N Carolina, Dept Chem & Biochem, Greensboro, NC 27412 USA
关键词
EPSPS; glyphosate; shikimate pathway; herbicide tolerance; X-ray crystallography; enzyme kinetics; 3-PHOSPHATE SYNTHASE; STRUCTURAL BASIS; RESISTANCE; SUBSTITUTION; EXPRESSION; PRO(101); MUTATION;
D O I
10.1021/acs.jafc.1c00439
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Natural and modified versions of the 5-enolpyruvylshikimate-3-phosphate synthase (epsps) gene have been used to confer tolerance to the broad-spectrum herbicide glyphosate in a variety of commercial crops. The most widely utilized trait was obtained from the Agrobacterium tumefaciens strain CP4 and has been commercialized in several glyphosate-tolerant crops. The EPSPS gene products are enzymes that have been divided into three classes based on sequence similarity, sensitivity to glyphosate, and steady-state catalytic parameters. Herein, we describe the informatics-guided identification and biochemical and structural characterization of a novel EPSPS from Streptomyces sviceus (DGT-28 EPSPS). The data suggest DGT-28 EPSPS and other closely related homologues exemplify a distinct new class (Class IV) of EPSPS enzymes that display intrinsic tolerance to high concentrations of glyphosate (K-i >= 5000 mu M). We further demonstrate that dgt-28 epsps, when transformed into stable plants, provides robust (>= 4x field rates) vegetative/reproductive herbicide tolerance and has utility in weed-control systems comparable to that of commercialized events.
引用
收藏
页码:5096 / 5104
页数:9
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