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Cesarino, I.

Publications and source records attributed to Cesarino, I..

2 recordsLinked to original sources

Three-dimensional nano-imaging reveals subtle changes in xylem structure in CAD-deficient sorghum

Lignin plays a central role in the formation and function of secondary cell walls in vascular plants. However, the structural consequences of lignin modification for cell wall properties and cellular function in grasses remain poorly understood. Here, we investigated how cinnamyl alcohol dehydrogenase (CAD) deficiency alters vascular cell architecture in Sorghum bicolor, using the brown midrib-6 (bmr6) mutant as a model system. Biochemical and histochemical analyses confirmed altered lignin chemistry in bmr6, including increased incorporation of hydroxycinnamaldehyde residues and reduced tricin levels. We applied ptychographic X-ray computed tomography (PXCT) to quantify the cell wall geometry, in three dimensions, at nanometer-scale resolution. PXCT enabled measurements of wall thickness distribution and lumen shape along tracheary elements. Analyses revealed no significant differences in wall thickness between wild-type and bmr6 plants. However, three-dimensional morphometric descriptors indicated reduced lumen convexity in bmr6, suggesting localized modifications not detectable by conventional two-dimensional imaging. Water flow numerical simulations through PXCT-derived images indicated reduced vessel permeability and simulated hydraulic conductivity in bmr6, suggesting that subtle geometric changes may influence performance. These findings highlight the value of three-dimensional imaging for resolving cell wall organization and provide new insight into the architectural resilience of grass xylem in response to targeted lignin modification. HighlightThree-dimensional X-ray nano-imaging reveals alterations in the cell wall architecture that affect simulated hydraulic performance under reduced CAD activity in sorghum.

plant biology↗

Gene Editing of Caffeic-O-methyltransferase (COMT1) in the model grass Setaria viridis Improves Biomass Saccharification Without Compromising Plant Growth or Abiotic Stress Tolerance

Second-generation bioethanol production is limited by the recalcitrance of lignocellulosic biomass, largely driven by lignin content and composition. Genetic strategies targeting lignin biosynthesis offer a promising alternative to improve biomass digestibility without relying on energy-intensive pretreatments. Here, we used CRISPR/Cas9 editing to disrupt the caffeic-O-methyltransferase gene (COMT1) in Setaria viridis, a C monocot model related to major bioenergy crops. COMT1 was selected based on its strong expression in lignifying tissues and its central role in the biosynthesis of syringyl (S) units, guaiacyl (G) units, and the flavone tricin, a non-canonical lignin monomer in grasses. Edited plants showed no visible growth defects, maintaining normal development and salt-stress tolerance. Chemical analyses revealed a drastic reduction in S units and tricin, accompanied by moderate but significant decreases in G and p-hydroxyphenyl (H) monomers. Despite these compositional changes, total soluble lignin content was only slightly reduced, suggesting compensatory incorporation of non-canonical monomers. Metabolome analysis of edited plants suggested a redirection of carbon flux towards phenylpropanoid and flavonoid pathways. These modifications resulted in a substantial increase in saccharification efficiency, demonstrating that COMT1 disruption can enhance biomass digestibility without compromising plant viability. Our findings highlight COMT1 as a key target for engineering improved feedstocks for bioenergy production. HighlightsCRISPR knockout of COMT1 in Setaria viridis markedly enhances biomass digestibility by reducing lignin monomers, without compromising plant growth or salt-stress tolerance. Genome editing of COMT1 in Setaria viridis reveals unexpected lignin plasticity, reducing S, G, H and tricin units and improving saccharification efficiency without developmental penalties. Combined thiacidolysis/GC-MS and metabolomics suggests a compensatory mechanism in the lignin portion of the S. viridis cell wall.

plant biology↗