Glufosinate

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Not to be confused with glyphosate.
Glufosinate
Skeletal formula of glufosinate
Ball-and-stick model of the glufosinate zwitterion
Names
IUPAC name
(RS)-2-Amino-4-(hydroxy(methyl)phosphonoyl)butanoic acid
Other names
Phosphinothricin
Identifiers
51276-47-2 YesY
ChEBI CHEBI:52136 YesY
ChEMBL ChEMBL450298 YesY
ChemSpider 4630 YesY
EC Number 257-102-5
Jmol 3D model Interactive image
KEGG C05042 YesY
PubChem 4794
  • InChI=1S/C5H12NO4P/c1-11(9,10)3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)(H,9,10) YesY
    Key: IAJOBQBIJHVGMQ-UHFFFAOYSA-N YesY
  • InChI=1/C5H12NO4P/c1-11(9,10)3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)(H,9,10)
    Key: IAJOBQBIJHVGMQ-UHFFFAOYAF
  • O=P(O)(CCC(C(=O)O)N)C
Properties
C5H12NO4P
Molar mass 181.13 g·mol−1
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Glufosinate (also known as phosphinothricin and often sold as an ammonium salt) is a broad-spectrum systemic herbicide with the chemical formula C5H15N2O4P. It irreversibly inhibits glutamine synthetase, an enzyme necessary for the production of glutamine and for ammonia detoxification. Application of glufosinate to plants leads to reduced glutamine and elevated ammonia levels in tissues, halting photosynthesis, resulting in plant death.[1]

Discovery

In the 1960s and early 1970s, scientists at University of Tübingen and at the Meiji Seika Kaisha Company independently discovered that species of Streptomyces produce a tripeptide they called bialaphos that inhibits bacteria; it consists of two alanine residues and a unique amino acid that is an analog of glutamate that they named "phosphinothricin."[2]:90 They determined that phosphinothricin irreversibly inhibits glutamine synthetase.[2]:90 Phosphinothricin was first synthesized by scientists at Hoechst in the 1970s as a racemic mixture; this racemic mixture is called glufosinate and is the commercially relevant version of the chemical.[2]:91-92

In the late 1980s scientists discovered enzymes in these Streptomyces species that selectively inactivate free phosphinothricin; the gene encoding the enzyme that was isolated from Streptomyces hygroscopicus was called the "bialaphos resistance" or "bar" gene, and the gene encoding the enzyme in Streptomyces viridochromeogenes was called "phosphinothricin acetyltransferase" or "pat".[2]:98 The two genes and their proteins have 80% homology on the DNA level and 86% amino acid homology, and are each 158 amino acids long.[2]:98

Use

Glufosinate is a broad-spectrum herbicide that is used to control important weeds such as morning glories, hemp sesbania (Sesbania bispinosa), Pennsylvania smartweed (Polygonum pensylvanicum) and yellow nutsedge similar to glyphosate. It is applied to young plants during early development for full effectiveness.[1] It is sold in formulations under brands including Basta, Rely, Finale, Challenge and Liberty.[1]

Glufosinate is typically used in three situations as an herbicide:

A crop sprayer

Glufosinate also has shown to provide some protection against various plant diseases, as it also acts to kill fungi and bacteria on contact.[4]

Genetically modified crops

Genetically modified crops resistant to glufosinate were created by genetically engineering the bar or pat genes from streptomyces into the relevant crop seeds.[2]:98[5] In 1995 the first glufosinate-resistant crop, canola, was brought to market, and it was followed by corn in 1997, cotton in 2004, and soybeans in 2011.[5]

Mode of action

Phosphinothricin is a glutamine synthetase inhibitor that binds to the glutamate site. Glufosinate-treated plants die due to a buildup of ammonia and corresponding decrease in pH in the thylakoid lumen, leading to the uncoupling of photophosphorylation.[4] The uncoupling of photophosphorylation causes the production of reactive oxygen species, lipid peroxidation, and membrane destruction.[6]

Elevated levels of ammonia are detectable within one hour after application of Phosphinothricin.[1]

Toxicity

Exposure to humans in foods

As glufosinate is often used as a pre-harvest desiccant, residues can also be found in foods that humans ingest. Such foods include potatoes, peas, beans, corn, wheat, and barley. In addition, the chemical can be passed to humans through animals who are fed contaminated straw. Flour processed from wheat grain that contained traces of glufosinate was found to retain 10-100% of the chemicals' residues.[7]

The herbicide is also persistent; it has been found to be prevalent in spinach, radishes, wheat and carrots that were planted 120 days after the treatment of the herbicide.[1] Its persistent nature can also be observed by its half-life which varies from 3 to 70 days depending on the soil type and organic matter content.[1] Residues can remain in frozen food for up to two years and the chemical is not easily destroyed by cooking the food item in boiling water.[7] The EPA classifies the chemical as 'persistent' and 'mobile' based on its lack of degradation and ease of transport through soil.

Exposure limits

There are no exposure limits established by the Occupational Safety & Health Administration or the American Conference of Governmental Industrial Hygienists.[8] The WHO/FAO recommended acceptable daily intake (ADI) for glufosinate is 0.02 mg/kg.[7] The European Food Safety Authority has set an ADI of 0.021 mg/kg. The Acute reference dose (ARfD) for child-bearing women is 0.021 mg/kg.[7]

Regulation

Glufosinate is a United States Environmental Protection Agency EPA registered chemical. It is also a California registered chemical. It is not banned in any country and it is not a PIC pesticide.[9] There are no exposure limits established by OSHA or the American Conference of Governmental Industrial Hygienists.[8]

Glufosinate is registered for use as an herbicide in Europe; it was last reviewed in 2007 and that registration was set to expire in 2018.[10]

References

  1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 Lua error in package.lua at line 80: module 'strict' not found.
  2. ↑ 2.0 2.1 2.2 2.3 2.4 2.5 Donn, G and Köcher, H. Inhibitors of Glutamine Synthetase. Chapter 4 in Herbicide Classes in Development: Mode of Action, Targets, Genetic Engineering, Chemistry. Eds Peter Böger, Ko Wakabayashi, Kenji Hirai. Springer Science & Business Media, 2012 ISBN 9783642594168
  3. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  4. ↑ 4.0 4.1 Duke, SO. Biotechnology: Herbicide Resistant Crops. In Encyclopedia of Agriculture and Food Systems, 2nd edition. Ed. Neal K. Van Alfen. Elsevier, 2014. ISBN 9780080931395. Page 97
  5. ↑ 5.0 5.1 Green JM and Castle LA. Transitioning from Single to Multiple Herbicide-resistant Crops. Chapter 4 in Glyphosate Resistance in Crops and Weeds: History, Development, and Management. Editor, Vijay K. Nandula. John Wiley & Sons, 2010 ISBN 9781118043547 Page 112
  6. ↑ Summary of Herbicide Mechanism of Action, HRAC and WSSA
  7. ↑ 7.0 7.1 7.2 7.3 Lua error in package.lua at line 80: module 'strict' not found.
  8. ↑ 8.0 8.1 Lua error in package.lua at line 80: module 'strict' not found.
  9. ↑ The Rotterdam Convention on Prior Informed Consent (PIC)
  10. ↑ European Commission. Glufosinate in EU Pesticides Database Page accessed August 7, 2015

External links

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