4.7 Article

Structural Imaging of Native Cryo-Preserved Secondary Cell Walls Reveals the Presence of Macrofibrils and Their Formation Requires Normal Cellulose, Lignin and Xylan Biosynthesis

Journal

FRONTIERS IN PLANT SCIENCE
Volume 10, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fpls.2019.01398

Keywords

scanning electron microscopy; cell walls; macrofibrils; cellulose; xylan; lignin; softwood; hardwood

Categories

Funding

  1. Leverhulme Trust Centre for Natural Material Innovation
  2. Center for Lignocellulose Structure and Formation, an Energy Frontier Research Center - U.S. Department of Energy (DOE), Office of Science, Basic Energy Sciences (BES) [DE-SC0001090]
  3. Biotechnology and Biological Sciences Research Council (BBSRC) of the UK as part of the Cambridge BBSRC-DTP Programme [BB/J014540/1]
  4. National Science Centre, Poland as part of the SONATINA 3 programme [2019/32/C/NZ3/00392]
  5. European Research Council Advanced Investigator Grant SYMDEV [323052]
  6. Finnish Centre of Excellence in Molecular Biology of Primary Producers (Academy of Finland CoE program 2014-2019) [271832]
  7. Gatsby Foundation [GAT3395/PR3]
  8. National Science Foundation Biotechnology and Biological Sciences Research Council grant [BB/N013158/1]
  9. University of Helsinki [799992091]
  10. BBSRC [BB/M015432/1]
  11. Gatsby Charitable Foundation
  12. BBSRC [BB/N013158/1] Funding Source: UKRI

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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 dependent upon the proper biosynthesis, or composed, of cellulose, xylan, and lignin. This study establishes that cryo-SEM 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.

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