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Afifi, O. A.

Publications and source records attributed to Afifi, O. A..

3 recordsLinked to original sources

Ultrastructural analysis of engineered rice lines reveals ferulate cross-linking as a key factor mediating lignocellulose supramolecular assembly in grass cell walls

Within the secondary cell walls of vascular plants, cellulose, hemicelluloses, and lignin associate via various covalent and non-covalent linkages to form an intricate supramolecular assembly. Although the chemical structures and cross-linking levels of the lignin- hemicellulose matrix exhibit substantial diversity in planta, precisely how these structural variations affect lignocellulose supramolecular assembly and macroscopic biomass properties remains largely elusive. Here, we conducted a comparative multi-scale ultrastructural analysis across engineered rice lines with targeted modifications in lignin aromatic composition and ferulate (FA)-mediated cell wall cross-linking levels. Combined solid-state nuclear magnetic resonance and wide-angle X-ray diffraction analyses revealed that depleting FA cross-linking disrupts cellulose crystalline structure and accelerates molecular mobility markedly more severely than altering the guaiacyl-to-syringyl (G/S) lignin ratio, generating a more loosened lignocellulose network. Small-angle X-ray scattering analysis further demonstrated that specific FA-depleted lines, but none of those with an altered G/S ratio, also exhibited disruptions in the nano- to mesoscale organization of cellulose microfibrils. Furthermore, FA- depleted lines generally displayed greater improvements in saccharification efficiency and more rapid thermal softening than G/S-lignin-altered lines, suggesting that disruptions in lignocellulose molecular assembly induced by FA depletion can broadly translate into macroscopic biomass properties. These findings establish a molecular basis for the pivotal role of FA cross-linking in dictating grass cell wall architecture, offering a promising structural target for advancing grass biomass utility and crop design.

plant biology↗

Stacked mutations disrupting syringyl and p-coumaroylated lignin biosynthesis in rice result in lignin dominated by guaiacyl units: insights into grass-specific lignin monomer biosynthesis and polymerization mechanisms

O_LIThe aromatic composition of lignin significantly impacts the usability of lignocellulosic biomass. In eudicots, transgenic and mutant lines with elevated guaiacyl (G) or syringyl (S) lignin units have been successfully generated by manipulating the expression level of CONIFERALDEHYDE 5-HYDROXYLASE (CAld5H). However, this bioengineering approach has proven less effective in grasses, implicating the potential existence of a grass-specific alternative pathway for S lignin biosynthesis. C_LIO_LIThrough characterization of genome-edited rice mutants, we demonstrated that S lignin in rice can be virtually eliminated by disrupting genes encoding CAld5H along with p- COUMAROYL-COENZYME A:MONOLIGNOL TRANSFERASE (PMT), a grass-specific enzyme essential for the biosynthesis of monolignol p-coumarate conjugates. In contrast, individual mutations in either CAld5H or PMT genes resulted in incomplete elimination of S lignin. These findings provide strong evidence that rice possesses a CAld5H-independent pathway leading to the grass-specific monolignol p-coumarate conjugates. C_LIO_LIIn-depth structural characterizations of G-dominated lignins from rice and Arabidopsis mutants, natural gymnosperm pine, and G-type synthetic lignin revealed pronounced effects of lineage-dependent cell wall environments on the linkage patterns and molecular weight distributions of the resulting lignin polymers. C_LIO_LIOverall, our findings highlight previously overlooked lineage-specific lignin monomer biosynthesis and polymerization patterns in grasses. C_LI

plant biology↗

Essential Yet Dispensable: The Role of CINNAMATE 4-HYDROXYLASE in Rice Cell Wall Lignification

A comprehensive understanding of the intricate lignin biosynthesis in grasses could contribute to enhancing our ability to utilize grass biomass. CINNAMATE 4-HYDROXYLASE (C4H), in conjunction with PHENYLALANINE AMMONIA-LYASE (PAL), initiates the entry of phenylalanine into the cinnamate/monolignol pathway, leading to the production of diverse phenylpropanoids, including lignin monomers. Despite extensive research on C4H in eudicots, genetic studies of C4H in grasses remain considerably limited. Notably, the role of C4H in the presence of PHENYLALANINE/TYROSINE AMMONIA-LYASE (PTAL), a grass-specific ammonia-lyase that can bypass the conserved PAL-C4H pathway by recruiting tyrosine into the cinnamate/monolignol pathway, remains unclear. To address this gap, a set of genome-edited rice mutants harboring knockout mutations in rice C4H genes were generated and subjected to the analysis of growth phenotype and cell wall chemotype, alongside isotopic feeding and chemical inhibitor assays to test the contributions of the PAL-C4H and PTAL pathways. The phenotype and chemotype characterizations of C4H-knockout rice mutants demonstrated that class I (OsC4H1/CYP73A38) and class II (OsC4H2a/CYP73A39 and OsC4H2b/CYP73A40) C4Hs cooperatively contribute to lignin biosynthesis in rice. Nevertheless, the impacts of C4H-deficiency on plant development and lignin formation in rice appeared to be less prominent compared to those reported in eudicots. The 13C-labeled phenylalanine and tyrosine feeding experiments demonstrated that even with the phenylalanine-derived PAL-C4H pathway completely blocked, the C4H-knockout rice can still produce significant levels of lignin and maintain sound cell walls by utilizing the tyrosine-derived PTAL pathway. Overall, this study demonstrates the essential but dispensable role of C4H in grass cell wall lignification.

plant biology↗