Inhibition by herbicides

Tissue Type. Most cell cultures are white and thus are not inhibited by herbicides whose single mode of action is via photosynthesis (P). Thus, one tissue type must be green in a universal pre-screen. A green in vitro system is not sufficient as some herbicides, e.g. napropamide, do not inhibit green cells (JJ). 

Metabolic methods based on precursor incorporation and vital staining are used to measure the extent of inhibition by herbicides. 

A. Rachon, P. Genix, Specificity of Plant Acetohydroxyacid Synthase Formation of Products and Inhibition by Herbicides, Plant Physiol. Biochem., 32, 473-477 (1994). 

Acetolactate synthase inhibition by herbicides, 36,38 inhibition by sulfonylurea herbicides, 33,36,37/... 

The growth inhibitory mechanism of the thiocarbamate herbicides, eg, EPTC, butylate, cycloate, diaHate, and triaHate, is not well defined. Cell elongation, rather than cell division, appears to be inhibited (183), although mitotic entry may be inhibited by diaHate (184). Thiocarbamates have a greater effect on shoot than toot tissue (163,184). The weU-documented inhibition of Hpid synthesis by thiocarbamates certainly contributes to the observed inhibitions of cell division and elongation. These compounds may also inhibit gibbereUic acid synthesis (185). 

Substances other than enzymes can be immobilized. Examples include the fixing of heparin on polytetrafluoroethylene with the aid of PEI (424), the controUed release of pesticides which are bound to PEI (425), and the inhibition of herbicide suspensions by addition of PEI (426). The uptake of anionic dyes by fabric or paper is improved if the paper is first catonized with PEI (427). In addition, PEI is able to absorb odorizing substances such as fatty acids and aldehydes. Because of its high molecular weight, PEI can be used in cosmetics and body care products, as weU as in industrial elimination of odors, such as the improvement of ambient air quaHty in sewage treatment plants (428). 

Fig. 3. Generation of propionyl-CoA from the isoleucine biosynthetic pathway. The intermediate 2-ketobutyrate can be decarboxylated by either the 2-oxoacid dehydrogenase complex or at low efficiency by the pyruvate dehydrogenase complex. Inhibition of the threonine deaminase by isoleucine and of the acetolactate synthase by herbicides are indicated with dashed arrows...

The conversion of fatty acids into very long chain fatty acids is specifically inhibited by the thiocarbamate herbicides such as EPTC and triallate (Figure 2.19). These compounds are used pre-plant incorporated for the control of grass and some small seeded broad-leaved weeds in crops such as maize and small grain cereals. 

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. 

The condensation of phospho-shikimic acid with phosphoenol pyruvate is catalyzed by the enzyme 3-enoylpyruvoylhikimate-5-phosphate synthase, or EPSP synthase for short. This reaction is specifically inhibited by the herbicide glyphosate. 

Interference by certain phenylurea and tf-phenylcarbamate herbicides with the photochemical reactions of isolated chloroplasts was first reported in 1956 (2). Over the next few years, inhibition by the s-triazines, uracils, benzimidazoles, and ben-zonitriles was reported 3, 6). ... 

R(+) enantiomer is herbicidally active (23.24). Hoppe and Zacher (12) showed that the R(+) enantiomer of diclofop was more effective than the S(-) enantiomer in reducing acetate incorporation into free fatty acids in isolated maize chloroplasts. ACCase activity is inhibited by R(+) (98% enantiomeric excess) haloxyfop acid but not by the S(-) (94% enantiomeric excess) enantiomer (Fig. 5). The inhibition caused by the S(-) enantiomer could be accounted for by the 3% contamination in the S(-) preparation by the R(+) enantiomer. 

The ALS isolated as described in Table III displayed typical Michaelis-Menten kinetics with respect to pyruvate with a Km of 2.44 mM. Substrate concentrations as high as 50x Km had no effect on the rate of the reaction. Thiamine pyrophosphate, FAD and Mg(2+) were an absolute requirement for catalysis by the purified enzyme. These properties are consistent with observations made by others (30). Optimum activity was obtained at pH 7.1 and 37C, which were also the best conditions for inhibition by TP. There was no significant difference in the 1(50) value of TP whether ALS was taken after step 2 or 5, indicating low potential for non-specific binding of the herbicide to other proteins. 

D also Interacts with lAA to reverse glyphosate growth Inhibition In tissue cultures (l i, 1701. but not In Intact plants (121) Extractable PAL activity In soybean seedlings was Inhibited by 2,4-D (1711 and 2,4-D lowered PAL activity Increases caused by glyphosate (1711. The herbicide has also been examined for Interactions of Induction and secretion of pathogenesis-related proteins In tobacco suspension cultures (1721. 

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