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Phytotoxic sites of action for molecular design of modern herbicides (Part 1): The photosynthetic electron transport system
Author(s) -
WAKABAYASHI KO,
BÖGER PETER
Publication year - 2004
Publication title -
weed biology and management
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.351
H-Index - 36
eISSN - 1445-6664
pISSN - 1444-6162
DOI - 10.1111/j.1445-6664.2003.00118.x
Subject(s) - photosynthesis , plastoquinone , biology , chloroplast , phytotoxicity , chlorophyll , site of action , electron transport chain , rational design , botany , computational biology , biochemistry , thylakoid , gene , genetics , endocrinology
A bird's eye review was tried to select the bio‐rational targets from known and novel plant‐specific ones for the molecular design of modern herbicides, which exhibit efficient phytotoxicity at a low‐use rate and preserve a good environment in the 21st century. In phytotoxic sites in the photosynthetic electron transport (PET) system discussed in the present article (Part 1), the generally called bleaching herbicides interfering with the biosynthesis of photosynthetic pigments, chlorophylls and carotenoids, and the biosynthesis of plastoquinone, were considered to be good models for the molecular design of modern herbicides. The PET itself was still considered as an interesting target site for new herbicides, although they need to exert their action in all green leaves of weeds to achieve herbicidal efficacy. Because these herbicides never form a tight binding with D1‐protein, their use‐rate cannot be expected to be as low as the herbicides inhibiting chlorophyll or branched amino‐acid biosynthesis. Other herbicidal targets found in chloroplasts, namely ATP and NADPH formations, have already been omitted from the worldwide biorational molecular design program of herbicides targeting the PET system.