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      Bipyrazone: a new HPPD-inhibiting herbicide in wheat

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          Abstract

          Bipyrazone, 1,3-dimethyl-4-(2-(methylsulfonyl)-4-(trifluoromethyl) benzoyl)-1H-pyrazol-5-yl 1,3-dimethyl-1H-pyrazole- 4-carboxylate, is a 4-hydroxyphenylpyaunate dioxygenase (HPPD)-inhibiting herbicide. Greenhouse and field experiments were conducted to explore the potential of post-emergence (POST) application of bipyrazone in wheat fields in China. In the greenhouse study, bipyrazone at 10 and 20 g active ingredient (a.i.) ha −1 effectively controlled Descurainia sophia L., Capsella bursa-pastoris (L.) Medic., Lithospermum arvense L. and Myosoton aquaticum L. Whereas, all tested 16 wheat cultivars showed high degree of tolerance to bipyrazone at 375 and 750 g a.i. ha −1. In a dose-response experiment carried on the Shannong 6 wheat cultivar and five weed biotypes, bipyrazone was safe to the wheat cultivar, and C. bursa-pastoris, M. aquaticum and D. sophia were sensitive to this herbicide. The selectivity index (SI) between the Shannong 6 and weeds ranged from 34 to 39. The field experiments confirmed that a mixture of bipyrazone and fluroxypyr-mepthyl is practical for controlling broadleaf weeds, and bipyrazone applied alone at 30 to 40 g a.i. ha −1 can also provide satisfactory control of sensitive broadleaf weeds. These findings suggest that bipyrazone POST application has good potential for broadleaf weed management in wheat fields.

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            Carotenoid biosynthesis in Arabidopsis: a colorful pathway.

            Plant carotenoids are a family of pigments that participate in light harvesting and are essential for photoprotection against excess light. Furthermore, they act as precursors for the production of apocarotenoid hormones such as abscisic acid and strigolactones. In this review, we summarize the current knowledge on the genes and enzymes of the carotenoid biosynthetic pathway (which is now almost completely elucidated) and on the regulation of carotenoid biosynthesis at both transcriptional and post-transcriptional levels. We also discuss the relevance of Arabidopsis as a model system for the study of carotenogenesis and how metabolic engineering approaches in this plant have taught important lessons for carotenoid biotechnology.
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              Metabolism-based herbicide resistance and cross-resistance in crop weeds: a threat to herbicide sustainability and global crop production.

              Weedy plant species that have evolved resistance to herbicides due to enhanced metabolic capacity to detoxify herbicides (metabolic resistance) are a major issue. Metabolic herbicide resistance in weedy plant species first became evident in the 1980s in Australia (in Lolium rigidum) and the United Kingdom (in Alopecurus myosuroides) and is now increasingly recognized in several crop-weed species as a looming threat to herbicide sustainability and thus world crop production. Metabolic resistance often confers resistance to herbicides of different chemical groups and sites of action and can extend to new herbicide(s). Cytochrome P450 monooxygenase, glycosyl transferase, and glutathione S-transferase are often implicated in herbicide metabolic resistance. However, precise biochemical and molecular genetic elucidation of metabolic resistance had been stalled until recently. Complex cytochrome P450 superfamilies, high genetic diversity in metabolic resistant weedy plant species (especially cross-pollinated species), and the complexity of genetic control of metabolic resistance have all been barriers to advances in understanding metabolic herbicide resistance. However, next-generation sequencing technologies and transcriptome-wide gene expression profiling are now revealing the genes endowing metabolic herbicide resistance in plants. This Update presents an historical review to current understanding of metabolic herbicide resistance evolution in weedy plant species.
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                Author and article information

                Contributors
                wangjx@sdau.edu.cn
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                26 March 2020
                26 March 2020
                2020
                : 10
                : 5521
                Affiliations
                [1 ]ISNI 0000 0000 9482 4676, GRID grid.440622.6, College of Plant Protection, , Shandong Agricultural University, ; Tai’an, 271018 Shandong P.R. China
                [2 ]ISNI 0000 0000 9482 4676, GRID grid.440622.6, Key Laboratory of Pesticide Toxicology and Application Technique, College of Plant Protection, , Shandong Agricultural University, ; Tai’an, 271018 Shandong P.R. China
                [3 ]Qingdao Kingagroot Chemical Compound Co., Ltd., Qingdao, 266000 Shandong P.R. China
                [4 ]Administration Bureau of the Yellow River Delta National Nature Reserve, Dongying, 257091 Shandong P.R. China
                Article
                62116
                10.1038/s41598-020-62116-6
                7098957
                32218463
                74ad9805-7d1c-49b4-88b7-582bc1948719
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 20 December 2018
                : 18 February 2020
                Funding
                Funded by: National Key R&D Program of China (2016YFD0300709, 2016YFD0300701), the Funds of “Shandong Double” Tops Program (No. SYL2017XTTD11) and the Major Science and Technology Innovation Project in Shandong Province (2018CXGC0213).
                Funded by: National Key R&D Program of China (2016YFD0300709, 2016YFD0300701), the Funds of “Shandong Double” Tops Program (No. SYL2017XTTD11) and the Major Science and Technology Innovation Project in Shandong Province (2018CXGC0213).
                Funded by: National Key R&D Program of China (2016YFD0300709, 2016YFD0300701), the Funds of “Shandong Double” Tops Program (No. SYL2017XTTD11) and the Major Science and Technology Innovation Project in Shandong Province (2018CXGC0213).
                Funded by: National Key R&D Program of China (2016YFD0300709, 2016YFD0300701), the Funds of “Shandong Double” Tops Program (No. SYL2017XTTD11) and the Major Science and Technology Innovation Project in Shandong Province (2018CXGC0213).
                Funded by: National Key R&D Program of China (2016YFD0300709, 2016YFD0300701), the Funds of “Shandong Double” Tops Program (No. SYL2017XTTD11) and the Major Science and Technology Innovation Project in Shandong Province (2018CXGC0213).
                Funded by: National Key R&D Program of China (2016YFD0300709, 2016YFD0300701), the Funds of “Shandong Double” Tops Program (No. SYL2017XTTD11) and the Major Science and Technology Innovation Project in Shandong Province (2018CXGC0213).
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                © The Author(s) 2020

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                drug safety,toxicology
                Uncategorized
                drug safety, toxicology

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