C on yza, Herbicide Resistance, ParaquatThe paper gives an overview of literature on paraquat resistance of weeds and the pro posed mechanism of resistance. New results we achieved on horseweed ( C onyza canadensis /L J, Cronq.) are discussed in detail.It was demonstrated that there is no significant constitutive difference related to the para quat resistance between untreated susceptible and paraquat-resistant horseweed plants. The lower sensitivity of flowering resistant plants may be due to the fact that paraquat content in treated leaves of flowering resistant plants was only 25% as compared to those measured at rosette stage. Our results confirm that paraquat resistance is not based on elevated level and activity of antioxidant enzyme system. The hypothesized role of polyam ines in the resis tance mechanisms can be excluded. The higher putrescine and total polyamine content of paraquat treated resistant leaves can rather be regarded as a general stress response, than as a symptom of paraquat resistance. A paraquat-inducible protein is supposed to play a role in the resistance, which presumably functions by binding paraquat to an inactivating site and/ or by carrying paraquat to metabolically inactive cell compartment (vacuole, cell wall). From m odel experiments it is concluded that paraquat and diquat preferentially form hydrophylic interactions with proteins containing a higher amount o f lysine and glutamic acid. C onse quently, the reason for paraquat resistance in horseweed is probably a hydrophylic interac tion of paraquat with a protein, leading to inactivation of paraquat through forming a conju gate and/or sequestration into the vacuole or the cell wall.
Bipyridyls and their mode of actionThe two best-known bipyridyl compounds, para quat (l,r-dim ethyl-4,4'-bipyridinium ) and diquat (9,10-dihydro-8a,10a-diazoniaphenanthrene), are used, generally in the form of haloid salts, as the active ingredients of post-emergent, non-selective, contact herbicides. These compounds are applied in vineyards, orchards and forests for total weed control, in horticulture for the weed control of seedbeds, and in the field for defoliation and desic cation of crops. These compounds are inactivated in the soil, as they bind irreversibly to clay miner als, so they have no residual effects. The com pounds are extremely toxic to vertebrates, and thus to man: the L D 50 value characterising the oral A bbreviations: LHCP, light harvesting chlorophyll pro tein complex; PqAR , paraquat/atrazine coresistant; PqR, paraquat-resistant; PS I, II, photosystem I, II; R, resistant; RF, resistance factor; S, susceptible; SOD, su peroxide dismutase. toxicity in rats is 157 mg/kg body weight for para quat. The minimum lethal dose by oral ingestion in human beings is about 35 mg/kg body weight. Because of the high toxicity the use of herbicides containing paraquat is severely restricted or banned in many E uropean countries. N everthe less, investigations on its effect and resistance mechanisms continue with scarcely diminished in tensity....