4.7 Article

Enhanced detoxification and degradation of herbicide atrazine by a group of O-methyltransferases in rice

期刊

CHEMOSPHERE
卷 165, 期 -, 页码 487-496

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2016.09.025

关键词

Rice (Oryza sativa); Atrazine; Methyltransferase; UPLC-LTQ-MS2

资金

  1. National Key Research and Development Project of China [2016YFD0200201]
  2. National Natural Science Foundation of China [21377058, 21577064]
  3. Special Fund for Agro-scientific Research in the Public Interest from Ministry of Agriculture of China [201203022]

向作者/读者索取更多资源

Atrazine (ATR) as a toxic herbicide has become one of the seriously environmental contaminants worldwide due to its long-term intensive use in crop production. This study identified novel methyltransferases (MTs) involved in detoxification and degradation of ATR residues in rice plants. From a subset of MTs differentially expressed in ATR-exposed rice, forty-four O-methyltransferase genes were investigated. Total activities were significantly enhanced by ATR in rice tissues. To prove detoxifying capacity of the MTs in rice plants, two rice O-MTs (LOC_Os04g09604 and LOC_Os11g15040) were selected and transformed into yeast cells (Pichia pastoris X-33). The positive transformants accumulated less ATR and showed less toxicity. Using UPLC-TOF-MS/MS, ATR-degraded products in rice and yeast cells were characterized. A novel O-methylated-modified metabolite (atraton) and six other ATR-derivatives were detected. The topological interaction between LOC_Os04g09604 enzyme and its substrate was specially analyzed by homology modeling programs, which was well confirmed by the molecular docking analysis. The significance of the study is to provide a better understanding of mechanisms for the specific detoxification and degradation of ATR residues in rice growing in environmentally relevant ATR-contaminated soils and may hold a potential engineering perspective for generating ATR-resistant rice that helps to minimize ATR residues in crops. (C) 2016 Elsevier Ltd. All rights reserved.

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