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A strategy to reduce the dose of multichiral agricultural chemicals: The herbicidal activity of metolachlor against Echinochloa crusgalli

机译:减少多手性农药用量的策略:异丙甲草胺对结E棘手chin的除草活性

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摘要

Agricultural chemicals are normally used as mixtures of several isomers, e.g., enantiomers. In theory, in order to minimize the pesticides dose, it is desirable to use the most target-active isomer. Metolachlor is a typical multichiral herbicide belonging to amide herbicides. An asymmetric carbon atom and a chiral axis yield four stereoisomers. In this study, a novel laboratory method was developed to prepare the S-metolachlor and the four stereoisomers using high performance liquid chromatography. The separated isomers had a purity of 99%, with their absolute configurations assigned by electronic circular dichroism. The enantioseparation by ultra performance convergence chromatography tandem mass spectrometry was also performed for the rapid and sensitive detection of metolachlor stereoisomers. The enantioselective herbicidal activity toward the target weed (Echinochloa crusgalli) was systematically assessed for the first time by measuring the morphology of the weed after treatment with rac-, S-metolachlor and the four stereoisomers, respectively. Among the commercial pesticides, S-metolachlor was more effective in weed inhibition than rac-metolachlor, and to the four stereoisomers, the herbicidal activities were ranked as: SS SR RS RR, and the RR-isomer even had some stimulative effect to the weed growth at lower concentration (1 ppm). Thus, we concluded that in these cases, the chiral carbon feature played a major role in herbicidal activity rather than the chiral axis feature, and the higher bioactivity of the S-isomers was confirmed by more effective uptake and stronger interaction with target enzymes that were involved in the gibberellic acid biosynthesis. Although the SS-isomer shows the highest herbicidal activity, controlling the major chiral feature is still much easier and more economical than controlling two chiral features. (C) 2019 Elsevier B.V. All rights reserved.
机译:农药通常以几种异构体(例如对映异构体)的混合物形式使用。从理论上讲,为了最大程度地减少农药用量,需要使用最具目标活性的异构体。甲草胺是一种典型的多手性除草剂,属于酰胺类除草剂。不对称碳原子和手性轴产生四个立体异构体。在这项研究中,开发了一种新型的实验室方法,以使用高效液相色谱法制备S-甲草胺和四种立体异构体。分离的异构体的纯度> 99%,其绝对构型由电子圆二色性指定。还通过超高效会合色谱串联质谱法进行了对映体分离,用于快速,灵敏地检测甲草胺立体异构体。通过分别测量rac-,S-异丙甲草胺和四种立体异构体处理后杂草的形态,首次系统地评估了对目标杂草(Echinochloa crusgalli)的对映选择性除草活性。在商品农药中,S-灭草胺的抑制杂草效果比rac-灭草胺更有效,并且对四种立体异构体的除草活性依次为:SS> SR> RS> RR,并且RR-异构体甚至具有一定的刺激性。较低浓度(1 ppm)对杂草的生长有影响。因此,我们得出结论,在这些情况下,手性碳特征在除草活性中起主要作用,而不是在手性轴特征中起作用,并且S-异构体的更高生物活性被更有效的吸收和与目标酶的更强相互作用所证实。参与赤霉素的生物合成。尽管SS-异构体显示出最高的除草活性,但控制主要的手性特征仍比控制两个手性特征容易得多且更经济。 (C)2019 Elsevier B.V.保留所有权利。

著录项

  • 来源
    《The Science of the Total Environment》 |2019年第10期|181-188|共8页
  • 作者单位

    Zhejiang Univ, MOE Key Lab Environm Remediat & Ecosyst Hlth, Coll Environm & Resource Sci, Hangzhou 310058, Zhejiang, Peoples R China;

    Zhejiang Univ, MOE Key Lab Environm Remediat & Ecosyst Hlth, Coll Environm & Resource Sci, Hangzhou 310058, Zhejiang, Peoples R China;

    Shanghai Ocean Univ, Coll Marine Ecol & Environm, Shanghai 201306, Peoples R China;

    Binzhou Univ, Coll Biol & Environm Engn, Binzhou 256600, Peoples R China;

    Zhejiang Univ, MOE Key Lab Environm Remediat & Ecosyst Hlth, Coll Environm & Resource Sci, Hangzhou 310058, Zhejiang, Peoples R China;

    Zhejiang Univ, MOE Key Lab Environm Remediat & Ecosyst Hlth, Coll Environm & Resource Sci, Hangzhou 310058, Zhejiang, Peoples R China;

    Zhejiang Univ, MOE Key Lab Environm Remediat & Ecosyst Hlth, Coll Environm & Resource Sci, Hangzhou 310058, Zhejiang, Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Metolachlor; HPLC; UPC2; Enantio-activity; Gibberellic acid;

    机译:MetOlachlor;HPLC;UPC2;肾性活性;凝胶酸;

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