Unravelling Phytotoxicity and Mode of Action of Tripyrasulfone, a Novel Herbicide

植物毒性 化学 光系统II 稗属 光合作用 紫黄质 甲基磺草酮 苯达松 植物 类胡萝卜素 立体化学 生物化学 生物 杂草 叶黄素 阿特拉津 玉米黄质 农学 杀虫剂
作者
Dandan Wang,Lipeng Wang,Xiaolin Zhang,Shuang Bai,Tao Jin,Weitang Liu,Jinxin Wang
出处
期刊:Journal of Agricultural and Food Chemistry [American Chemical Society]
卷期号:69 (25): 7168-7177 被引量:28
标识
DOI:10.1021/acs.jafc.1c01294
摘要

Tripyrasulfone is a novel herbicide post-emergence applied in paddy fields. In this study, tripyrasulfone phytotoxicity and its mode of action were investigated. Within 3-7 days after treatment (DAT), tripyrasulfone caused strong bleaching symptoms on newly developed leaves of Echinochloa crus-galli followed by necrosis prior to death within 14 DAT. By investigating pigment composition, photosynthetic activity and energy dissipation of E. crus-galli treated with tripyrasulfone, the accumulation of phytoene and significant decreases in total carotenoids were observed; the photosystem II complex (PSII) reaction center and PSII-PSI electron transport chain were damaged; and the non-photochemical energy quenching and reactive oxygen species were significantly increased. Based on the reversion of bleaching symptoms in treated Spirodela polyrrhiza by the addition of homogentisic acid, it was hypothesized that tripyrasulfone blocks the biosynthesis of HGA, possibly by the inhibition of 4-hydroxyphenylpyruvate dioxygenase (HPPD). However, based on its chemical structure, tripyrasulfone may tend to be hydrolyzed in plants. Indeed, the hydrolyzed tripyrasulfone (HDT) inhibited the activity of HPPD from Arabidopsis thaliana produced by Escherichia coli, which was approximately 6 times less effective than mesotrione. Molecular docking showed that the HDT formed a stable bidentate interaction with the active center Fe2+ chelation of A. thaliana HPPD.
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