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Metabolism of Herbicides or Xenobiotics in Plants

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Metabolism of Herbicides or Xenobiotics in Plants - Phase I - Oxidation Reactions

Oxidation - (Figure 1) Oxidation reactions are some of the most common xenobiotic transformations occurring in plants.

Fig. 1: Oxidation

These Phase I reactions result in either detoxication or activation of the herbicide. Many of these oxidative reactions are presumed to be catalyzed by cytochrome P-450 monooxygenases. Monoxygenases catalyze reactions in which one of the two atoms of molecular oxygen is incorporated into the substrate (e.g. herbicide or xenobiotic) and the atom is reduced to water by an electron donor, such as NADPH (equation 1).


Equation 1:

X + RH2 + O2 → X-O + H2O + R

Where, X is the substrate (e.g. xenobiotic, herbicide), RH2 is the reduced cofactor such as NADPH, O2 is required as the second substrate, X-O is the oxygenated product and RH is the oxidized cofactor. Cytochrome P-450 monooxygenases are usually membrane bound and xenobiotic metabolism occurs in the endoplasmic reticulum.

Examples of oxidation reactions include N-dealkylation or N-demethylation (Figure 2), O-dealkylation (Figure 3), aromatic hydroxylation (Figure 4), thioether oxidation (Figure 5) and β-oxidation (Figure 6).
 

Fig. 2: N-dealkylation or N-demethylation Fig. 3: O-dealkylation Fig. 4: Aromatic hydroxylation

Fig. 5a: Thioether oxidation - initially produces a sulfoxide, a molecule with less phytotoxicity Fig. 5b: Thioether oxidation - the sulfoxide can be conjugated with glutathione or further oxidized (Figure 5c) Fig. 5c: Thioether oxidation - the sulfoxide is converted to a sulfate, a molecule with less phytotoxicity

Fig. 6: β-oxidation

Some insecticides (organophosphates) can act as suicide substrates, irreversibly binding to cytochrome P450s in the plant and rendering the crop more sensitive to some herbicides (e.g. sulfonylureas). On the other hand, safeners or antagonists are able to induce (increase) cytochrome P450 monooxygenases in protected grass crops and therefore, enhance metabolism of some herbicides in the aryloxyphenoxypropionate, sulfonylurea, imidazolinone and sulfonamide families.
 

Can inhibiting the enzymes that detoxify pesticides, alter the pesticide’s toxicity?

 

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