Oral Presentation 26th ACMM “2020 Visions in Microscopy”

Fluorescence microscopy enables linking flavonoid localisation and function in legume roots (#86)

Ulrike Mathesius 1 , Pinhui Wang 1 , Jason Ng 1 , Anton Wasson 2
  1. Australian National University, Canberra, ACT, Australia
  2. CSIRO Agriculture, CSIRO, Canberra, ACT, Australia

Legumes are distinguished by their ability to develop root nodules in symbiosis with nitrogen-fixing rhizobia. Flavonoids are essential signals during the symbiosis, first as Nod gene inducers acting on the rhizobia, secondly as regulators of auxin transport and auxin localisation (Wasson et al., 2006). Due to their autofluorescence and the specificity of their fluorescence emission spectra, fluorescence microscopy can be used to easily localise and party identify flavonoids in situ (Mathesius et al., 1998)  We have combined the localisation of flavonoids with mass spectrometry to identify and quantify flavonoid structures, and have linked this to their functions in controlling auxin localisation in legume roots (Ng et al., 2015). While flavonoids accumulate specifically in dividing cells of a number of roots organs, including nodules, lateral roots and root galls, flavonoids are only essential for nodule development (Wasson et al., 2009). This suggests that nodulation in legumes has recruited flavonoids for this novel organogenesis process. The localisation of specific flavonoids is correlated with the accumulation of auxin, with flavonoids acting as auxin transport inhibitors in those cells, as well as in regulating enzymes involved in generation and quenching of reactive oxygen species (Mathesius 2001; Ng et al., 2015).

 

Mathesius et al. (1998)  Molec. Plant-Microbe Interact. 11: 1223-1232

Mathesius (2001)  J. Exp.Bot. 52: 419-426

Ng et al. (2015)  Plant Cell 27: 2210-2226

Wasson et al. (2006) Plant Cell 18, 1617-1629

Wasson et al. (2009) New Phytol. 183: 167–179