Pseudomonas effector AvrB is a glycosyltransferase that rhamnosylates plant guardee protein RIN4

  • Sci Adv. 2024 Feb 16;10(7):eadd5108. doi: 10.1126/sciadv.add5108.
Wei Peng  1  2 Nalleli Garcia  3 Kelly A Servage  1  2 Jennifer J Kohler  4 Joseph M Ready  4 Diana R Tomchick  4  5 Jessie Fernandez  3 Kim Orth  1  2  4
Affiliations
  • 1. Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • 2. Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • 3. Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL, USA.
  • 4. Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • 5. Department of Biophysics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Abstract

The plant pathogen Pseudomonas syringae encodes a type III secretion system avirulence effector protein, AvrB, that induces a form of programmed cell death called the hypersensitive response in Plants as a defense mechanism against systemic Infection. Despite the well-documented catalytic activities observed in Other Fido ( Fi c, Do c, and AvrB) proteins, the enzymatic activity and target substrates of AvrB have remained elusive. Here, we show that AvrB is an unprecedented Glycosyltransferase that transfers rhamnose from UDP-rhamnose to a threonine residue of the Arabidopsis guardee protein RIN4. We report structures of various enzymatic states of the AvrB-catalyzed rhamnosylation reaction of RIN4, which reveal the structural and mechanistic basis for rhamnosylation by a Fido protein. Collectively, our results uncover an unexpected reaction performed by a prototypical member of the Fido superfamily while providing important insights into the plant hypersensitive response pathway and foreshadowing more diverse chemistry used by Fido proteins and their substrates.

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