EPSP synthase

Nomenclature

The enzyme belongs to the family of transferases, to be specific those transferring aryl or alkyl groups other than methyl groups. The systematic name of this enzyme class is phosphoenolpyruvate:3-phosphoshikimate 5-O-(1-carboxyvinyl)-transferase. Other names in common use include:

• 5-enolpyruvylshikimate-3-phosphate synthase,
• 3-enolpyruvylshikimate 5-phosphate synthase,
• 3-enolpyruvylshikimic acid-5-phosphate synthetase,
• 5′-enolpyruvylshikimate-3-phosphate synthase,
• 5-enolpyruvyl-3-phosphoshikimate synthase,
• 5-enolpyruvylshikimate-3-phosphate synthetase,
• 5-enolpyruvylshikimate-3-phosphoric acid synthase,
• enolpyruvylshikimate phosphate synthase, and
• 3-phosphoshikimate 1-carboxyvinyl transferase.

Structure

EPSP synthase is a monomeric enzyme with a molecular mass of approximately 46,000. It consists of two domains connected by protein strands that function as a hinge, allowing the two domains to move closer together. When a substrate binds to the enzyme, the conformational change causes the domains to clamp around the substrate at the active site.

EPSP synthase is classified into two groups based on sensitivity to glyphosate. Class I enzymes, found in plants and some bacteria, are inhibited by low micromolar concentrations of glyphosate. Class II enzymes, found in other bacteria, are resistant to glyphosate inhibition.

Shikimate pathway

EPSP synthase participates in the biosynthesis of the aromatic amino acids phenylalanine, tyrosine, and tryptophan via the shikimate pathway in bacteria, fungi, and plants. EPSP synthase is produced only by plants and micro-organisms; the gene coding for it is not in the mammalian genome. Gut flora of some animals contain EPSPS.

Reaction

EPSP synthase catalyzes the reaction which converts shikimate-3-phosphate plus phosphoenolpyruvate to 5-enolpyruvylshikimate-3-phosphate (EPSP) by way of an acetal-like tetrahedral intermediate. Basic and acidic amino acids in the active site are involved in deprotonation of the hydroxyl group of PEP and in the proton-exchange steps related to the tetrahedral intermediate itself, respectively.

Studies of the enzyme kinetics for this reaction have determined the specific sequence and energetics of each step of the process. A neutrally charged lysine (lys-22) acts as a general base, deprotonating the hydroxyl group of S3P such that the resulting oxyanion can attack the most electrophilic carbon atom of PEP. A glutamic acid (glu-341) acts as a general acid by donating a proton. The deprotonated glu-341 then acts as a base, taking back its proton, and the S3P group is kicked off and protonated by the protonated lysine.

Herbicide target

EPSP synthase is the biological target for the herbicide glyphosate. Glyphosate is a competitive inhibitor of EPSP synthase, acting as a transition state analog that binds more tightly to the EPSPS-S3P complex than PEP and inhibits the shikimate pathway. This binding leads to inhibition of the enzyme's catalysis and shuts down the pathway. Eventually this results in organism death from lack of aromatic amino acids the organism requires to survive.

A version of the enzyme that both was resistant to glyphosate and that was still efficient enough to drive adequate plant growth was identified by Monsanto scientists after much trial and error in an Agrobacterium strain called CP4 (). The strain CP4 was found surviving in a waste-fed column at a glyphosate production facility. The CP4 EPSP synthase enzyme has been engineered into several genetically modified crops.

References

References

1. (October 2005). "Molecular basis for the glyphosate-insensitivity of the reaction of 5-enolpyruvylshikimate 3-phosphate synthase with shikimate". FEBS Letters.
2. (1990). "Gene amplification in glyphosate-tolerant tobacco cells". Plant Science.
3. (December 1985). "Crystallization of 5-enolpyruvylshikimate 3-phosphate synthase from ''Escherichia coli''". Journal of Molecular Biology.
4. (May 1988). "Purification and Properties of 5-Enolpyruvylshikimate-3-Phosphate Synthase from Dark-Grown Seedlings of Sorghum bicolor". Plant Physiology.
5. (August 2011). "Molecular basis of glyphosate resistance-different approaches through protein". The FEBS Journal.
6. (August 2006). "Molecular basis for the herbicide resistance of Roundup Ready crops". Proceedings of the National Academy of Sciences of the United States of America.
7. (2012). "The shikimate pathway and aromatic amino Acid biosynthesis in plants". Annual Review of Plant Biology.
8. (2006). "The current status and environmental impacts of glyphosate-resistant crops: a review". Journal of Environmental Quality.
9. (2010). "Comprehensive Natural Products II. Chemistry and Biology.".
10. (February 1990). "Observation by 13C NMR of the EPSP synthase tetrahedral intermediate bound to the enzyme active site". Biochemistry.
11. (February 2004). "Structural studies of Streptococcus pneumoniae EPSP synthase in unliganded state, tetrahedral intermediate-bound state and S3P-GLP-bound state". Molecular Microbiology.
12. (September 1988). "A tetrahedral intermediate in the EPSP synthase reaction observed by rapid quench kinetics". Biochemistry.
13. (December 2020). "Investigation of the target-site resistance of EPSP synthase mutants P106T and T102I/P106S against glyphosate". RSC Advances.
14. (February 2001). "Interaction of the herbicide glyphosate with its target enzyme 5-enolpyruvylshikimate 3-phosphate synthase in atomic detail". Proceedings of the National Academy of Sciences of the United States of America.