Glyphosate, Roundup

Roundup, 13 38-39, 19 53, 8 2 Roundup/Glyphosate, 2 549t Roundup Ready cottons, 8 2 Roundup tolerance, engineering, 12 487-490... 

S. Shoval, S. Yariv, The interaction between roundup (glyphosate) and montmorillonite Part 1, Infrared study of the sorption of glyphosate by montmorillonite. Clays Clay Miner. 27, 19-28 (1979)... 

A/-(phosphonomethyl)-glyciae isopropylamiae salt [38641-94-0 ] [22224-92-6 ] [26264-05-1 ] From Diisopropylamine [2303-16-4] Roundup / glyphosate herbicide... 

Transgenic soybean plants expressing the CTP-CP4 EPSPS display commercial levels of Roundup tolerance. These results vaUdate the importance of substrate kinetics of EPSPS in order to maintain adequate rates of aromatic biosynthesis. Furthermore, the fact that glyphosate tolerance can be obtained by expression of a glyphosate-tolerant EPSPS illustrates that the herbicidal mode of action of glyphosate is related solely to inhibition of the EPSPS reaction. 

Progress in Heterocyclic Chemistiy (PHC) Volume 9 reviews critically the heterocyclic literature published mainly in 1996. The first two chapters are review articles. Chapter 1 by C.J. Moody and K.J. Doyle deals with "The Synthesis of Oxazoles from Diazocarbonyl Compounds," and Chapter 2 by J.A. Sikorski provides a detailed account of the heterocyclic chemistry suiTounding the remarkable herbicide glyphosate ("Roundup" ). This latter chapter illustrates the role that heterocyclic chemistry plays in other areas of modem chemistry, since glyphosate is a far cry from being heterocyclic ... 

Precursors of phenylpropanoids are synthesized from two basic pathways the shikimic acid pathway and the malonic pathway (see Fig. 3.1). The shikimic acid pathway produces most plant phenolics, whereas the malonic pathway, which is an important source of phenolics in fungi and bacteria, is less significant in higher plants. The shikimate pathway converts simple carbohydrate precursors into the amino acids phenylalanine and tyrosine. The synthesis of an intermediate in this pathway, shikimic acid, is blocked by the broad-spectrum herbicide glyphosate (i.e., Roundup). Because animals do not possess this synthetic pathway, they have no way to synthesize the three aromatic amino acids (i.e., phenylalanine, tyrosine, and tryptophan), which are therefore essential nutrients in animal diets. 

Enthusiasm for chemicals by the industry and the public, however, went largely unabated, and indeed the number and range of available and recommended chemicals began to multiply in this period, with specialized formulations targeted at specific weed and insect problems. Aldrin, carbaryl, diazinon, Dicamba, meta-chlorophenylpiperazine (MCPP), chlorpyrifos, Carbaryl, Pyrethrum, and Dacthal (DCPA) all found their way to consumer markets in the next few years, capped by the arrival of glyphosate (known most commonly by its trade name Roundup ). Despite setbacks (as in the case of DDT), the chemical approach to lawn care has become normal and widespread, with more households using these chemicals every year. 

Other carboxylic acids that have become popular herbicides, though they are not phenoxyacetic acid derivatives, are dicamba and glyphosate or Roundup . Notice that dicamba does have a methoxy group and two chlorines, so it is similar to 2,4-D. Glyphosate is used on cotton and... 

For example, the EU recently cleared the herbicide glyphosate (Roundup), which is practically nontoxic to humans, for consumer use. Nevertheless, KEMI has notified importers and distributors that sales of glyphosate to the public will be severely restricted in the future. Faithful to its socialist traditions, the almighty Swedish State attaches no value to the billions of Swedish crowns invested by private homeowners in lawns, flowerbeds, rose gardens, and so on. An appeal to KEMI s decision will most likely be directed to the European Court of Justice. 

All carbons are derived from either erythrose 4-phosphate (light purple) or phosphoenolpyruvate (pink). Note that the NAD+ required as a cofactor in step (3) is released unchanged it may be transiently reduced to NADH during the reaction, with formation of an oxidized reaction intermediate. Step (6) is competitively inhibited by glyphosate (COO—CH2—NH—CH2—PO ), the active ingredient in the widely used herbicide Roundup. The herbicide is relatively nontoxic to mammals, which lack this biosynthetic pathway. The chemical names quinate, shikimate, and chorismate are derived from the names of plants in which these intermediates have been found to accumulate. 

In recent years, agribusiness firms have developed pf empirically several compounds that inhibit essential steps in the biosynthesis of amino acids found in plants but missing in animals. One of these compounds, glyphosate, is a highly specific inhibitor of 5-enol pyruvyl-shikimate-3-phosphate synthase (an enzyme needed for aromatic amino acid biosynthesis). Glyphosate is the active ingredient in the widely used herbicide Roundup. 

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