Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1971 Jul 1;50(1):63–80. doi: 10.1083/jcb.50.1.63

LIGNOFIBRILS ON THE EXTERNAL CELL WALL SURFACE OF CULTURED PLANT CELLS

Gary G Leppard 1, J Ross Colvin 1, Dyson Rose 1, S M Martin 1
PMCID: PMC2108420  PMID: 5563452

Abstract

Small strands and bundles of strands extend from the outside surface of suspension-cultured cells of Daucus, Ipomoea, and Phaseolus into the medium. This fibrous cell coat is present in all samples from various growth stages but appears to increase in quantity in the order Ipomoea < Phaseolus < Daucus. The bundles are often many microns in length and display great variation in frequency, size, and form. Identification of the composition of the strands and bundles as lignin is consistent with the following observations: alkaline nitrobenzene oxidation of the strands to compounds which resemble monomers of wood lignin; resistance of the strands to pronase, trypsin, pectinase, and lipase; strong irreversible adsorption of heavy metals; deposition of silver granules by treatment with silver nitrate-hexamine reagent; extraction of the bundles with aqueous dioxane (Björkman procedure); presence in quantity of a structured form of Klason lignin; and existence of material giving a positive test with the Wiesner reagent. Large individual strands (lignofibrils) from Phaseolus show the form of a flat ribbon with very thin branches at irregular intervals. This form does not vary with preparatory techniques, although its electron opacity does. Intercellular spaces display considerable structure and sometimes contain sheets of fibrillar material merging with both the middle lamella between the cells and the surface bundles facing the medium. These sheets are probably another form of association of the lignofibrils. It is suggested that natural fibrous lignin may be a much commoner component of plant tissue than suspected hitherto.

Full Text

The Full Text of this article is available as a PDF (2.0 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Aspinall G. O., Molloy J. A., Craig J. W. Extracellular polysaccharides from suspension-cultured sycamore cells. Can J Biochem. 1969 Nov;47(11):1063–1070. doi: 10.1139/o69-170. [DOI] [PubMed] [Google Scholar]
  2. Cocking E. C. Virus uptake, cell wall regeneration, and virus multiplication in isolated plant protoplasts. Int Rev Cytol. 1970;28:89–124. doi: 10.1016/s0074-7696(08)62541-3. [DOI] [PubMed] [Google Scholar]
  3. Gamborg O. L. Aromatic metabolism in plants. II. Enzymes of the shikimate pathway in suspension cultures of plant cells. Can J Biochem. 1966 Jun;44(6):791–799. doi: 10.1139/o66-097. [DOI] [PubMed] [Google Scholar]
  4. Gamborg O. L. Aromatic metabolism in plants. V. The biosynthesis of chlorogenic acid and lignin in potato cell cultures. Can J Biochem. 1967 Sep;45(9):1451–1457. doi: 10.1139/o67-171. [DOI] [PubMed] [Google Scholar]
  5. Halperin W., Jensen W. A. Ultrastructural changes during growth and embryogenesis in carrot cell cultures. J Ultrastruct Res. 1967 May;18(3):428–443. doi: 10.1016/s0022-5320(67)80128-x. [DOI] [PubMed] [Google Scholar]
  6. LUFT J. H. Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol. 1961 Feb;9:409–414. doi: 10.1083/jcb.9.2.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Luft J. H. Fine structures of capillary and endocapillary layer as revealed by ruthenium red. Fed Proc. 1966 Nov-Dec;25(6):1773–1783. [PubMed] [Google Scholar]
  8. Olson A. C., Evans J. J., Frederick D. P., Jansen E. F. Plant suspension culture media macromolecules-pectic substances, protein, and peroxidase. Plant Physiol. 1969 Nov;44(11):1594–1600. doi: 10.1104/pp.44.11.1594. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Pickett-Heaps J. D. Further ultrastructural observations on polysaccharide localization in plant cells. J Cell Sci. 1968 Mar;3(1):55–64. doi: 10.1242/jcs.3.1.55. [DOI] [PubMed] [Google Scholar]
  10. Pickett-Heaps J. D. Preliminary attempts at ultrastructural polysaccharide localization in root tip cells. J Histochem Cytochem. 1967 Aug;15(8):442–455. doi: 10.1177/15.8.442. [DOI] [PubMed] [Google Scholar]
  11. Power J. B., Cummins S. E., Cocking E. C. Fusion of isolated plant protoplasts. Nature. 1970 Mar 14;225(5237):1016–1018. doi: 10.1038/2251016a0. [DOI] [PubMed] [Google Scholar]
  12. SABATINI D. D., BENSCH K., BARRNETT R. J. Cytochemistry and electron microscopy. The preservation of cellular ultrastructure and enzymatic activity by aldehyde fixation. J Cell Biol. 1963 Apr;17:19–58. doi: 10.1083/jcb.17.1.19. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Swift J. A. The electron histochemistry of cystine--containing proteins in thin transverse sections of human hair. J R Microsc Soc. 1968;88(4):449–460. doi: 10.1111/j.1365-2818.1968.tb00626.x. [DOI] [PubMed] [Google Scholar]
  14. TREVELYAN W. E., PROCTER D. P., HARRISON J. S. Detection of sugars on paper chromatograms. Nature. 1950 Sep 9;166(4219):444–445. doi: 10.1038/166444b0. [DOI] [PubMed] [Google Scholar]
  15. Thompson E., Colvin J. R. Electron cytochemical localization of cystine in plant cell walls. J Microsc. 1970 Apr;91(2):87–98. doi: 10.1111/j.1365-2818.1970.tb02210.x. [DOI] [PubMed] [Google Scholar]
  16. Veliky I. A., Martin S. M. A fermenter for plant cell suspension cultures. Can J Microbiol. 1970 Apr;16(4):223–226. doi: 10.1139/m70-041. [DOI] [PubMed] [Google Scholar]
  17. WATSON M. L. Staining of tissue sections for electron microscopy with heavy metals. J Biophys Biochem Cytol. 1958 Jul 25;4(4):475–478. doi: 10.1083/jcb.4.4.475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Yaguchi M., Perry M. B. Ion exchange chromatography of 2-amino-2-deoxy-D-hexoses. Can J Biochem. 1970 Mar;48(3):386–388. doi: 10.1139/o70-062. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES