Transformation of the Herbicide Sulcotrione into a Root Growth Enhancer Compound by Sequential Photolysis and Hydrolysis

J Agric Food Chem. 2016 Jan 27;64(3):563-9. doi: 10.1021/acs.jafc.5b05500. Epub 2016 Jan 11.

Abstract

Xanthene-1,9-dione-3,4-dihydro-6-methylsulfonyl (1), the main product of sulcotrione phototransformation on plant leaves, was slowly hydrolyzed into 2-hydroxy-4-methylsulfonylbenzoic acid (2) and 1,3-cyclohexanedione (3) in aqueous solution. Interestingly, the rate of hydrolysis was significantly enhanced in the presence of roots of monocotyledonous plants, while the same treatment showed adverse effects on broadleaf weeds. Root growth enhancement varied according to the plant species and concentrations of compound 2, as shown with Zea mays roots. Compound 2 is a derivative of salicylic acid that is known to be a plant signaling messenger. Compound 2 was, therefore, able to mimic some known effects of this phytohormone. This work showed that a pesticide like sulcotrione was transformed into a compound exhibiting a positive impact on plant growth. This study exemplified a rarely reported situation where chemical and biological chain reactions transformed a xenobiotic into a compound exhibiting potential beneficial effects.

Keywords: hydrolysis; photoproducts; plant root growth; salicylic acid derivative; sulcotrione.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclohexanones / chemistry*
  • Cyclohexanones / pharmacology
  • Herbicides / chemistry*
  • Herbicides / pharmacology
  • Hydrolysis
  • Mesylates / chemistry*
  • Mesylates / pharmacology
  • Molecular Structure
  • Photolysis
  • Plant Roots / drug effects
  • Plant Roots / growth & development*
  • Zea mays / drug effects*
  • Zea mays / growth & development

Substances

  • Cyclohexanones
  • Herbicides
  • Mesylates
  • sulcotrione