Bacterial pathogen deploys the iminosugar glycosyrin to manipulate plant glycobiology

The extracellular space (apoplast) in plants is a key battleground during microbial infections. To avoid recognition, the bacterial model phytopathogen <i>Pseudomonas syringae</i> pv. <i>tomato</i> DC3000 produces glycosyrin. Glycosyrin inhibits the plant-secreted β-galactosidase BGAL1, which would otherwise initiate the release of immunogenic peptides from bacterial flagellin. Here, we report the structure, biosynthesis, and multifunctional roles of glycosyrin. High-resolution cryo-electron microscopy and chemical synthesis revealed that glycosyrin is an iminosugar with a five-membered pyrrolidine ring and a hydrated aldehyde that mimics monosaccharides. Glycosyrin biosynthesis was controlled by virulence regulators, and its production is common in bacteria and prevents flagellin recognition and alters the extracellular glycoproteome and metabolome of infected plants. These findings highlight a potentially wider role for glycobiology manipulation by plant pathogens across the plant kingdom.

Authors

Institutions

Publication Details

Journal
Science
Published
2025-04-17
DOI
https://doi.org/10.1126/science.adp2433
Citations
4
Primary Topic
Plant Pathogenic Bacteria Studies
Type
article
Field-Weighted Citation Impact
7.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Bacterial pathogen deploys the iminosugar glycosyrin to manipulate plant glycobiology

Nattapong Sanguankiattichai, Gail M. Preston, Richard Strasser, Markus Kaiser et al.
4 citations
Science
Plant Pathogenic Bacteria Studies
7.00
article

Bacterial pathogen deploys the iminosugar glycosyrin to manipulate plant glycobiology

Nattapong Sanguankiattichai, Gail M. Preston, Richard Strasser, Markus Kaiser, Daniel Krahn, Pierre Buscaill, Margit Drapal, Clemens Grünwald‐Gruber, Suzuka Yamamoto, Farnusch Kaschani, Balakumaran Chandrasekar, Yuewen Sheng, Atsushi Kato, Nathan Hardenbrook, Renier A. L. van der Hoorn, Robert J. Nash, Peijun Zhang, George W. J. Fleet, Werner W. A. Tabak
article en
4 citations

Abstract

The extracellular space (apoplast) in plants is a key battleground during microbial infections. To avoid recognition, the bacterial model phytopathogen <i>Pseudomonas syringae</i> pv. <i>tomato</i> DC3000 produces glycosyrin. Glycosyrin inhibits the plant-secreted β-galactosidase BGAL1, which would otherwise initiate the release of immunogenic peptides from bacterial flagellin. Here, we report the structure, biosynthesis, and multifunctional roles of glycosyrin. High-resolution cryo-electron microscopy and chemical synthesis revealed that glycosyrin is an iminosugar with a five-membered pyrrolidine ring and a hydrated aldehyde that mimics monosaccharides. Glycosyrin biosynthesis was controlled by virulence regulators, and its production is common in bacteria and prevents flagellin recognition and alters the extracellular glycoproteome and metabolome of infected plants. These findings highlight a potentially wider role for glycobiology manipulation by plant pathogens across the plant kingdom.

ScienceVol. 388(6744)
Centre for Human Genetics (GB), Royal Holloway University of London (GB), Mahidol University (TH), Diamond Light Source (GB), University of Oxford (GB), Leibniz Institute for Analytical Sciences - ISAS (DE), Vienna Biocenter (AT), Toyama University Hospital (JP), Institute of Biological, Environmental and Rural Sciences (GB), University of Toyama (JP), University of Duisburg-Essen (DE), BOKU University (AT)
Openalex Percentile: Top 4%
Plant Pathogenic Bacteria Studies
7.00
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.