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新型原卟啉原氧化酶抑制剂除草剂噻呋酰胺的生化和生理作用模式。

Biochemical and physiological mode of action of tiafenacil, a new protoporphyrinogen IX oxidase-inhibiting herbicide.

机构信息

FarmHannong Co., Ltd., Yeoui-daero 24, Yeongdeungpo-gu, Seoul 07320, Republic of Korea.

Korean Agency for Technology and Standards, Isu-ro 93, Maengdong-myeon, Eumseong-gun, Chungcheongbuk-do 27737, Republic of Korea.

出版信息

Pestic Biochem Physiol. 2018 Nov;152:38-44. doi: 10.1016/j.pestbp.2018.08.010. Epub 2018 Aug 24.

Abstract

We conducted biochemical and physiological experiments to investigate the mode of action of tiafenacil (Terrad'or™), a new protoporphyrinogen IX oxidase (PPO)-inhibiting pyrimidinedione herbicide. Analysis of the half-maximal inhibitory concentration (IC) against recombinant PPO enzymes from various plant species, including amaranth (Amaranthus tuberculatus), soybean (Glycine max), arabidopsis (Arabidopsis thaliana), and rapeseed (Brassica napus), showed that tiafenacil had an IC of 22 to 28 nM, similar to the pyrimidinedione herbicides butafenacil and saflufenacil and the N-phenylphthalimide herbicide flumioxazin. By contrast, tiafenacil exhibited 3- to 134-fold lower IC values than the diphenyl ether herbicides fomesafen, oxyfluorfen, and acifluorfen. Tiafenacil is non-selective and is herbicidal to both dicots and monocots, such as the weeds velvetleaf (Abutilon theophrasti), amaranth, and barnyardgrass (Echinochloa crus-galli) as well as the crops soybean, rapeseed, rice (Oryza sativa), and maize (Zea mays) at concentrations ranging from 1 to 50 μM. Treatment of plant tissue with tiafenacil in darkness resulted in the accumulation of protoporphyrin IX. Subsequent exposure to light increased the content of malondialdehyde and significantly decreased the Fv/Fm values of chlorophyll fluorescence. The results suggest that tiafenacil is a new PPO-inhibiting pyrimidinedione herbicide.

摘要

我们进行了生化和生理实验,以研究新型原卟啉原氧化酶(PPO)抑制剂嘧啶二酮类除草剂噻吩嘧啶(Terrad'orTM)的作用模式。分析来自不同植物物种的重组 PPO 酶(包括苋菜(Amaranthus tuberculatus)、大豆(Glycine max)、拟南芥(Arabidopsis thaliana)和油菜(Brassica napus))的半最大抑制浓度(IC)表明,噻吩嘧啶对 PPO 的抑制作用与嘧啶二酮类除草剂丁氟消、唑嘧磺草胺类似,IC 为 22-28 nM。相比之下,噻吩嘧啶对二苯醚类除草剂氟磺胺草醚、乳氟禾草灵和乙羧氟草醚的 IC 值低 3-134 倍。噻吩嘧啶无选择性,对双子叶和单子叶杂草均具有杀草活性,如空心莲子草、苋菜和稗草,以及大豆、油菜、水稻和玉米等作物,其有效浓度范围为 1-50 μM。黑暗条件下用噻吩嘧啶处理植物组织会导致原卟啉 IX 的积累。随后暴露在光下会增加丙二醛的含量,并显著降低叶绿素荧光的 Fv/Fm 值。结果表明,噻吩嘧啶是一种新型的 PPO 抑制剂嘧啶二酮类除草剂。

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