Cell twisting during desiccation reveals axial asymmetry in wall organization

Plant cell size and shape are tuned to their function and specified primarily by cellulose microfibril (CMF) patterning of the cell wall. Arabidopsis thaliana leaf trichomes are responsible for protecting plants against environmental elements and are unicellular structures that employ a highly anisotropic cellulose wall to extend and taper, generating pointed branches. During elongation, the mechanisms by which shifts in fiber orientation generate cells with predictable sizes and shapes are unknown. Specifically, the axisymmetric growth of trichome branches is often thought result from axisymmetric CMF patterning. Here, we analyzed the direction and degree of twist of branches after desiccation to reveal the presence of an asymmetric cell wall organization with a left-hand bias. CMF organization, quantified using computational modeling, suggests a limited reorientation of microfibrils during growth and maximum branch length limited by the wall axial stiffness. The model provides a mechanism for CMF asymmetry, which occurs after the branch bending stiffness becomes low enough that ambient bending affects the principal stresses. After this stage, the CMF synthesis results in a constant bending stiffness for longer branches. The resulting natural frequency of branches after a length of 200 μm falls within the range of the sounds associated with many insects.

Microspheres and Nanorods Produced in the Dissolution of Mildly Carboxylated Cellulose Fibers in Alkaline Solutions

A mild etherification of spruce kraft pulp was performed to introduce 1.3 and 2.5 mmol/g carboxyl groups on cellulose chains. 1.3 mmol/g carboxymethyl fibers (CMF) were dissolved partially in alkaline water to form balloons and collars on the tracheid and their ultra-structure was investigated. Primary wall, expanded S1, swollen S2, wrinkled S3, spiral bands of S1, parallel microfibrils of S2 and their transverse splitting were observed on swollen fibers. It is indicated that balloons, collars and wrinkled S3 were formed due to different cellulose microfibril features in different layers of tracheid cell wall. Microspheres with a size up to about 0.6 µm were observed by field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM). It is shown that they originated from transverse splitting of S2 microfibrils and contain bundles of well-known cellulose nanocrystals (CNC). After homogenization and sonication of an aqueous dispersion of 2.5 mmol/g CMF, electroacoustic spectroscopy showed the presence of nanorods with a size distribution of 18-208 nm. Similar sizes were observed by TEM.

Callose: a multifunctional (1, 3)-β–d-glucan involved in morphogenesis and function of angiosperm stomata

Background Although the cellulose microfibril organization in guard cell (GC) walls play a crucial role in the mechanism of the stomatal function, recent work showed that matrix cell wall materials are also involved. Especially in the kidney-shaped stomata of the fern Asplenium nidus, callose actively participates in the mechanism of opening and closure of the stomatal pore. Scope The present review briefly presents and discusses recent findings concerning the distribution and role of callose in the kidney-shaped stomata of the dicotyledon Vigna sinensis as well as in the dumbbell-shaped stomata of the monocotyledon Zea mays. Conclusion The discussed data support that, in both categories of angiosperm stomata, callose is implicated in the mechanism of stomatal pore formation and stomata function by locally affecting the mechanical properties of the GC cell walls.

A TEMPO-catalyzed oxidation-reduction method to probe surface and anhydrous crystalline-core domains of cellulose microfibril bundles

A modified TEMPO-catalyzed oxidation of the solvent-exposed glucosyl units of cellulose to uronic acids, followed by carboxyl reduction with NaBD 4 to 6-deutero- and 6,6-dideuteroglucosyl units, provided a robust method for determining relative proportions of disordered amorphous, ordered surface chains, and anhydrous core-crystalline residues of cellulose microfibrils inaccessible to TEMPO. Both glucosyl residues of cellobiose units, digested from amorphous chains of cellulose with a combination of cellulase and cellobiohydrolase, were deuterated, whereas those from anhydrous chains were undeuterated. By contrast, solvent-exposed and anhydrous residues alternate in surface chains, so only one of the two residues of cellobiosyl units was labeled. Although current estimates indicate that each cellulose microfibril comprises only 18 to 24 (1 , 4)- b eta-D-glucan chains, we show here that microfibrils of walls of Arabidopsis leaves and maize coleoptiles, and those of secondary wall cellulose of cotton fibers and poplar wood, bundle into much larger macrofibrils, with 67 to 86% of the glucan chains in the anhydrous domain. These results indicate extensive bundling of microfibrils into macrofibrils occurs during both primary and secondary wall formation. We discuss how, beyond lignin, the degree of bundling into macrofibrils contributes an additional recalcitrance factor to lignocellulosic biomass for enzymatic or chemical catalytic conversion to biofuel substrates.

Online measurement of floc size, viscosity, and consistency of cellulose microfibril suspensions with optical coherence tomography

In this study, cellulose microfibril (CMF) suspensions were imaged during pipe flow at consistencies of 0.4%, 1.0%, and 1.6% with optical coherence tomography (OCT) to obtain images of the structure and the local velocity of the suspension. The viscosities obtained by combining pressure loss measurement with the OCT velocity data showed typical shear thinning behavior and were in excellent agreement with viscosities obtained with ultrasound velocity profiling. The structural OCT images were used to calculate the radial and the axial floc sizes of the suspension. A fit of power law to the geometrical floc size–shear stress data gave the same power law index for all consistencies, suggesting that floc rupture dynamics is independent of consistency. The dependence of viscosity and floc size on shear stress was similar, indicating that the shear thinning behavior of CMF suspensions is closely related to the rupture dynamics of flocs. The results also showed that an apparent attenuation coefficient of the OCT signal can be used to determine the consistency of CMF suspensions.

Comparative studies on wood structure and microtensile properties between compression and opposite wood fibers of Chinese fir plantation

The microtensile properties of mechanically isolated compression wood (CW) and opposite wood (OW) tracheids of Chinese fir (Cunninghamia lanceolata) were investigated and discussed with respect to their structure. Major differences in the tensile modulus and ultimate tensile stress were found between CW and OW fibers. Compared to OW, CW showed a larger cellulose microfibril angle, less cellulose content and probably more pits, resulting in lower tensile properties. These findings contribute to a further understanding of the structural–mechanical relationships of Chinese fir wood at the cell and cell wall level, and provide a scientific basis for better utilization of plantation softwood.