10
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Physiological basis for isoxadifen-ethyl induction of nicosulfuron detoxification in maize hybrids

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Isoxadifen-ethyl can effectively alleviate nicosulfuron injury in the maize. However, the effects of safener isoxadifen-ethyl on detoxifying enzymes in maize is unknown. The individual and combined effects of the sulfonylurea herbicide nicosulfuron and the safener isoxadifen-ethyl on the growth and selected physiological processes of maize were evaluated. Bioassays showed that the EC 50 values of nicosulfuron and nicosulfuron plus isoxadifen-ethyl for maize cultivar Zhengdan958 were 18.87 and 249.28 mg kg -1, respectively, and were 24.8 and 275.51 mg kg -1, respectively, for Zhenghuangnuo No. 2 cultivar. Evaluations of the target enzyme of acetolactate synthase showed that the I 50 values of nicosulfuron and nicosulfuron plus isoxadifen-ethyl for the ALS of Zhengdan958 were 15.46 and 28.56 μmol L -1, respectively, and were 0.57 and 2.17 μmol L -1, respectively, for the acetolactate synthase of Zhenghuangnuo No. 2. The safener isoxadifen-ethyl significantly enhanced tolerance of maize to nicosulfuron. The enhanced tolerance of maize to nicosulfuron in the presence of the safener, coupled with the enhanced injury observed in the presence of piperonyl butoxide, 1-aminobenzotriazole, and malathion, suggested cytochrome P450 monooxygenases may be involved in metabolism of nicosulfuron. We proposed that isoxadifen-ethyl increases plant metabolism of nicosulfuron through non-P450-catalyzed routes or through P450 monooxygenases not inhibited by piperonyl butoxide, 1-aminobenzotriazole, and malathion. Isoxadifen-ethyl, at a rate of 33 mg kg -1, completely reversed the effects of all doses (37.5–300 mg kg -1) of nicosulfuron on both of the maize cultivars. When the two compounds were given simultaneously, isoxadifen-ethyl enhanced activity of glutathione S-transferases (GSTs) and acetolactate synthase activity in maize. The free acid 4,5-dihydro-5,5-diphenyl-1,2-oxazole-3-carboxylic was equally effective at inducing GSTs as the parent ester and appeared to be the active safener. GST induction in the maize Zhenghuangnuo No. 2 was faster than in Zhengdan 958.

          Related collections

          Most cited references42

          • Record: found
          • Abstract: found
          • Article: not found

          Multiple roles for plant glutathione transferases in xenobiotic detoxification.

          Discovered 40 years ago, plant glutathione transferases (GSTs) now have a well-established role in determining herbicide metabolism and selectivity in crops and weeds. Within the GST superfamily, the numerous and plant-specific phi (F) and tau (U) classes are largely responsible for catalyzing glutathione-dependent reactions with xenobiotics, notably conjugation leading to detoxification and, more rarely, bioactivating isomerizations. In total, the crystal structures of 10 plant GSTs have been solved and a highly conserved N-terminal glutathione binding domain and structurally diverse C-terminal hydrophobic domain identified, along with key coordinating residues. Unlike drug-detoxifying mammalian GSTs, plant enzymes utlilize a catalytic serine in place of a tyrosine residue. Both GSTFs and GSTUs undergo changes in structure during catalysis indicative of an induced fit mechanism on substrate binding, with an understanding of plant GST structure/function allowing these proteins to be engineered for novel functions in detoxification and ligand recognition. Several major crops produce alternative thiols, with GSTUs shown to use homoglutathione in preference to glutathione, in herbicide detoxification reactions in soybeans. Similarly, hydroxymethylglutathione is used, in addition to glutathione in detoxifying the herbicide fenoxaprop in wheat. Following GST action, plants are able to rapidly process glutathione conjugates by at least two distinct pathways, with the available evidence suggesting these function in an organ- and species-specific manner. Roles for GSTs in endogenous metabolism are less well defined, with the enzymes linked to a diverse range of functions, including signaling, counteracting oxidative stress, and detoxifying and transporting secondary metabolites.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Detoxification without intoxication: herbicide safeners activate plant defense gene expression.

              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Old Enzymes for a New Job (Herbicide Detoxification in Plants).

                Bookmark

                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                7 March 2017
                2017
                : 12
                : 3
                : e0173502
                Affiliations
                [1 ]Department of Plant Protection, Shenyang Agricultural University, Shenyang, China
                [2 ]Institute of Plant Protection, Henan Academy of Agricultural Sciences, Zhengzhou, China
                Clemson University, UNITED STATES
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                • Conceptualization: LS RW.

                • Data curation: LS RW WS ZG.

                • Formal analysis: LS RW.

                • Funding acquisition: ZG CL.

                • Investigation: LS RW WS.

                • Methodology: LS RW.

                • Project administration: ZG CL.

                • Resources: LS RW WS.

                • Software: LS RW WS.

                • Supervision: LS RW WS ZG.

                • Validation: LS RW WS.

                • Visualization: LS RW WS.

                • Writing – original draft: LS RW.

                • Writing – review & editing: LS RW ZG.

                Article
                PONE-D-16-49583
                10.1371/journal.pone.0173502
                5340377
                28267798
                3a065f5e-987d-4b10-87e5-0d4282089bed
                © 2017 Sun et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 15 December 2016
                : 21 February 2017
                Page count
                Figures: 7, Tables: 1, Pages: 16
                Funding
                Funded by: the Special Fund for Agro-scientific Research in the Public Interest
                Award ID: 201203098
                Award Recipient :
                The present study has been supported by the Special Fund for Agro-scientific Research in the Public Interest (201203098).
                Categories
                Research Article
                Research and Analysis Methods
                Experimental Organism Systems
                Model Organisms
                Maize
                Research and Analysis Methods
                Model Organisms
                Maize
                Biology and Life Sciences
                Organisms
                Plants
                Grasses
                Maize
                Research and Analysis Methods
                Experimental Organism Systems
                Plant and Algal Models
                Maize
                Biology and Life Sciences
                Agriculture
                Agrochemicals
                Herbicides
                Physical Sciences
                Chemistry
                Chemical Compounds
                Organic Compounds
                Ethers
                Organophosphates
                Malathion
                Physical Sciences
                Chemistry
                Organic Chemistry
                Organic Compounds
                Ethers
                Organophosphates
                Malathion
                Research and Analysis Methods
                Chromatographic Techniques
                Affinity Chromatography
                Amino Acid Specific Chromatography
                Glutathione Chromatography
                Biology and Life Sciences
                Toxicology
                Detoxification
                Medicine and Health Sciences
                Pathology and Laboratory Medicine
                Toxicology
                Detoxification
                Biology and Life Sciences
                Biochemistry
                Metabolism
                Metabolic Pathways
                Xenobiotic Metabolism
                Biology and Life Sciences
                Biochemistry
                Enzymology
                Enzyme Chemistry
                Enzyme Metabolism
                Biology and Life Sciences
                Organisms
                Plants
                Seedlings
                Custom metadata
                All relevant data are within the paper.

                Uncategorized
                Uncategorized

                Comments

                Comment on this article