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Triazine Probes Target Ascorbate Peroxidases in Plants.

Kyoko MorimotoKyle S ColeJiorgos KourelisCollin H WittDaniel BrownDaniel KrahnMonika StegmannFarnusch KaschaniMarkus KaiserJonathan W BurtonShabaz MohammedKazuko Yamaguchi-ShinozakiEranthie Weerapanavan der Hoorn Renier A L
Published in: Plant physiology (2019)
Though they are rare in nature, anthropogenic 1,3,5-triazines have been used in herbicides as chemically stable scaffolds. Here, we show that small 1,3,5-triazines selectively target ascorbate peroxidases (APXs) in Arabidopsis (Arabidopsis thaliana), tomato (Solanum lycopersicum), rice (Oryza sativa), maize (Zea mays), liverwort (Marchantia polymorpha), and other plant species. The alkyne-tagged 2-chloro-4-methyl-1,3,5-triazine probe KSC-3 selectively binds APX enzymes, both in crude extracts and in living cells. KSC-3 blocks APX activity, thereby reducing photosynthetic activity under moderate light stress, even in apx1 mutant plants. This suggests that APX enzymes in addition to APX1 protect the photosystem against reactive oxygen species. Profiling APX1 with KCS-3 revealed that the catabolic products of atrazine (a 1,3,5-triazine herbicide), which are common soil pollutants, also target APX1. Thus, KSC-3 is a powerful chemical probe to study APX enzymes in the plant kingdom.
Keyphrases
  • living cells
  • fluorescent probe
  • arabidopsis thaliana
  • reactive oxygen species
  • single molecule
  • single cell
  • transcription factor
  • small molecule
  • high resolution
  • mass spectrometry
  • photodynamic therapy