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Hydroxyphenylpyruvate Dioxygenase HPPD - the Herbicide Target

Breitenbach, P. Boger, G. Sandmarm, Pestic. Biochem. Physiol. 2002, 73, 104-109. [Pg.211]

Mitchel, in Synthesis and Chemistry of Agrochemicals IV, D. R. Baker, J. G. Fenyes, G. S. Basarab (Eds.), ACS Symposium Series 584, American Chemical Society, Washington, D.C. 1995, 161-170. [Pg.211]

Yamada, K. Aral, K. Hirase, K. Moriyasu, C. Schneider, [Pg.211]

Sandmann, P. Boger, K. Waka-bayashi. Pest. Manag. Sci., 2001, 57, 33-40. [Pg.211]

Crop Prot. Conf. -Weeds 1999, 1, 41-52. [Pg.211]


HydroxYphenYlpyruvate Dioxygenase (HPPD) - the Herbicide Target 219 Table 4.2.1 Estimated inhibition constants of HPPD inhibitors. [Pg.219]

The molecular target site of triketone herbicides is the enzyme -hydroxyphenylpyruvate dioxygenase (HPPD). Inhibition of this enzyme disrupts the biosynthesis of carotenoids and causes a bleaching (loss of chlorophyll) effect on the foliage similar to that observed with inhibitors ofphytoene desaturase (e.g. norflurazon). However, the mechanism of action of HPPD inhibitors is different. Inhibtion of HPPD stops the synthesis of homogen tisate (HGA), which is a key precursor of the 8 different tocochromanols (tocopherols and tocotrienols) and prenyl quinones. In the absence of prenylquinone plastoquinone, phytoene desaturase activity is interrupted. The bleaching of the green tissues ensues as if these compounds inhibited phytoene desaturase. [Pg.240]


See other pages where Hydroxyphenylpyruvate Dioxygenase HPPD - the Herbicide Target is mentioned: [Pg.211]    [Pg.211]    [Pg.215]    [Pg.217]    [Pg.211]    [Pg.211]    [Pg.215]    [Pg.217]    [Pg.147]    [Pg.148]    [Pg.178]    [Pg.105]    [Pg.106]    [Pg.287]    [Pg.156]    [Pg.603]   


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4-Hydroxyphenylpyruvic

Dioxygenases

Herbicides targets

Hydroxyphenylpyruvate

Hydroxyphenylpyruvate dioxygenase

The target

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