Abstract
The woody secondary cell walls of plants are the largest repository of renewable carbon biopolymers on the planet. These walls are made principally from cellulose and hemicelluloses and are impregnated with lignin. Despite their importance as the main load bearing structure for plant growth, as well as their industrial importance as both a material and energy source, the precise arrangement of these constituents within the cell wall is not yet fully understood. We have adapted low temperature scanning electron microscopy (cryo-SEM) for imaging the nanoscale architecture of angiosperm and gymnosperm cell walls in their native hydrated state. Our work confirms that cell wall macrofibrils, cylindrical structures with a diameter exceeding 10 nm, are a common feature of the native hardwood and softwood samples. We have observed these same structures in Arabidopsis thaliana secondary cell walls, enabling macrofibrils to be compared between mutant lines that are perturbed in cellulose, hemicellulose and lignin formation. Our analysis indicates that the macrofibrils in Arabidopsis cell walls are composed, at least partially, of cellulose, xylan and lignin. This study is a useful additional approach for investigating the native nanoscale architecture and composition of hardwood and softwood secondary cell walls and demonstrates the applicability of Arabidopsis genetic resources to relate fibril structure with wall composition and biosynthesis.
List of abbreviations
- 1D
- one dimensional
- AFM
- atomic force microscopy CesA – Cellulose
- synthase cryo-SEM
- low temperature scanning electron
- microscopy FE-SEM
- field emission scanning electron microscopy
- FT-IR
- Fourier-transform infrared spectroscopy
- GGM
- galactoglucomannan
- He-ion
- Helium ion
- IRX
- irregular xylem
- [Me]GlcA
- methylated and unmethylated form of glucuronic acid
- NMR
- nuclear magnetic resonance
- SANS
- small angle neutron scattering
- TEM
- transmission electron microscopy
- WAXS
- wide angle x-ray scattering