Planta

, Volume 235, Issue 6, pp 1209–1219 | Cite as

Ultrastructure of the innermost surface of differentiating normal and compression wood tracheids as revealed by field emission scanning electron microscopy

  • Jong Sik Kim
  • Tatsuya Awano
  • Arata Yoshinaga
  • Keiji Takabe
Original Article

Abstract

The ultrastructure of the innermost surface of Cryptomeria japonica differentiating normal wood (NW) and compression wood (CW) was comparatively investigated by field emission electron microscopy (FE-SEM) combined with enzymatic degradation of hemicelluloses. Cellulose microfibril (CMF) bundles were readily observed in NW tracheids in the early stage of secondary cell wall formation, but not in CW tracheids because of the heavy accumulation of amorphous materials composed mainly of galactans and lignin. This result suggests that the ultrastructural deposition of cell wall components in the tracheid cell wall differ between NW and CW from the early stage of secondary cell wall formation. Delignified NW and CW tracheids showed similar structural changes during differentiating stages after xylanase or β-mannanase treatment, whereas they exhibited clear differences in ultrastructure in mature stages. Although thin CMF bundles were exposed in both delignified mature NW and CW tracheids by xylanase treatment, ultrastructural changes following β-mannanase treatment were only observed in CW tracheids. CW tracheids also showed different degradation patterns between xylanase and β-mannanase. CMF bundles showed a smooth surface in delignified mature CW tracheids treated with xylanase, whereas they had an uneven surface in delignified mature CW tracheids treated with β-mannanase, indicating that the uneven surface of CMF bundles was related to xylans. The present results suggest that ultrastructural deposition and organization of lignin and hemicelluloses in CW tracheids may differ from those of NW tracheids.

Keywords

Cellulose microfibril Compression wood Cryptomeria japonica FE-SEM Hemicellulose Lignin 

Abbreviations

CMF

Cellulose microfibril

CW

Compression wood

NW

Normal wood

Notes

Acknowledgments

Jong Sik Kim is grateful for the Research Fellowship for Young Scientists provided by the Japan Society for the Promotion of Science (JSPS).

References

  1. Atalla R (2005) The role of the hemicelluloses in the nanobiology of wood cell walls. A systems theoretic perspective. In: Proceedings of the hemicelluloses workshop 2005. University of Canterbury, Christchurch, pp 37–57Google Scholar
  2. Awano T, Takabe K, Fujita M (2002) Xylan deposition on secondary wall of Fagus crenata fiber. Protoplasma 219:106–115PubMedCrossRefGoogle Scholar
  3. Baird WM, Johnson MA, Parham RA (1974) Development and composition of the warty layer in balsam fir. II. Composition. Wood and Fiber 6:211–222Google Scholar
  4. Côté WA, Day AC (1962) Vestured pits—fine structure and apparent relationship with warts. Tappi 45:906–910Google Scholar
  5. Côté WA Jr, Pickard PA, Timell TE (1967) Studies on compression wood. IV. Fractional extraction and preliminary characterization of polysaccharides in normal and compression wood of Balsam fir. Tappi 50:350–356Google Scholar
  6. Donaldson LA (2001) Lignification and lignin topochemistry—an ultrastructural view. Phytochemistry 57:859–873PubMedCrossRefGoogle Scholar
  7. Donaldson L (2007) Cellulose microfibril aggregates and their size variation with cell wall type. Wood Sci Technol 41:443–460CrossRefGoogle Scholar
  8. Hoffmann GC, Timell TE (1972) Polysaccharides in compression wood of tamarack (Larix laricina). 2. Constitution of a galactoglucomannan. Svensk Paperstidn 75:297–298Google Scholar
  9. Iwata T, Indrarti L, Azuma J (1998) Affinity of hemicellulose for cellulose produced by Acetobacter xylinum. Cellulose 5:215–218CrossRefGoogle Scholar
  10. Kim JS, Awano T, Yoshinaga A, Takabe K (2010) Immunolocalization of β-1-4-galactan and its relationship with lignin distribution in developing compression wood of Cryptomeria japonica. Planta 232:109–119PubMedCrossRefGoogle Scholar
  11. Kim JS, Awano T, Yoshinaga A, Takabe K (2011) Occurrence of xylan and mannan polysaccharides and their spatial relationship with other cell wall components in differentiating compression wood tracheids of Cryptomeria japonica. Planta 233:721–735PubMedCrossRefGoogle Scholar
  12. Nanayakkara B, Manley-Harris M, Suckling ID, Donaldson LA (2009) Quantitative chemical indicators to assess the gradation of compression wood. Holzforschung 63:431–439CrossRefGoogle Scholar
  13. Ruel K, Chevalier-Billosta V, Guillemin F, Sierra JB, Joseleau J-P (2006) The wood cell wall at the ultrastructural scale-formation and topochemical organization. Maderas Ciencia y Tecnologiá 8:107–116Google Scholar
  14. Salmén L, Burgert I (2009) Cell wall features with regard to mechanical performance. Holzforschung 63:121–129CrossRefGoogle Scholar
  15. Terashima N, Awano T, Takabe K, Yoshida M (2004) Formation of macromolecular lignin in ginko xylem cell walls as observed by field emission scanning electron microscopy. C R Biologie 327:903–910CrossRefGoogle Scholar
  16. Terashima N, Kitano K, Kojima M, Yoshida M, Yamamoto H, Westermark U (2009) Nanostructural assembly of cellulose, hemicellulose, and lignin in the middle layer of secondary wall of ginko tracheid. J Wood Sci 55:409–416CrossRefGoogle Scholar
  17. Timell TE (1986) Compression wood in gymnosperms, vol 1. Springer-Verlag, BerlinGoogle Scholar
  18. Tokoh C, Takabe K, Fujita M, Saiki H (1998) Cellulose synthesized by Acetobacter xylinum in the presence of acetyl glucomannan. Cellulose 5:249–261CrossRefGoogle Scholar
  19. Tokoh C, Takabe K, Sugiyama J, Fujita M (2002a) Cellulose synthesized by Acetobacter xylinum in the presence of plant cell wall polysaccharides. Cellulose 9:65–74CrossRefGoogle Scholar
  20. Tokoh C, Takabe K, Sugiyama J, Fujita M (2002b) CP/MAS 13C NMR and electron diffraction study of bacterial cellulose structure affected by cell wall polysaccharides. Cellulose 9:351–360CrossRefGoogle Scholar
  21. Uhlin KI, Atalla RH, Thompson NS (1995) Influence of hemicelluloses on the aggregation patterns of bacterial cellulose. Cellulose 2:129–144CrossRefGoogle Scholar
  22. Yeh TF, Goldfarb B, Chang HM, Peszlen L, Braun JL, Kadla JF (2005) Comparison of morphological and chemical properties between juvenile wood and compression wood of loblolly pine. Holzforschung 59:669–674CrossRefGoogle Scholar
  23. Yeh TF, Braun JL, Goldfarb B, Chang HM, Kadla JF (2006) Morphological and chemical variations between juvenile wood, mature wood, and compression wood of loblolly pine (Pinus taeda L.). Holzforschung 60:1–8CrossRefGoogle Scholar

Copyright information

© Springer-Verlag 2011

Authors and Affiliations

  • Jong Sik Kim
    • 1
    • 2
  • Tatsuya Awano
    • 1
  • Arata Yoshinaga
    • 1
  • Keiji Takabe
    • 1
  1. 1.Laboratory of Tree Cell Biology, Graduate School of AgricultureKyoto UniversityKyotoJapan
  2. 2.Wood Science, Department of Forest ProductsSwedish University of Agricultural SciencesUppsalaSweden

Personalised recommendations