Skip to main content
Log in

Microwave-stimulated glutaraldehyde and osmium tetroxide fixation of plant tissue: ultrastructural preservation in seconds

  • Published:
Histochemistry Aims and scope Submit manuscript

Summary

Microwave-enhanced fixation of animal tissues for electron microscopy has gained in interest in recent years. Attempts to use microwave irradiation for the preparation of plant tissues are rare. In this study, I report on microwave conditions which allow a high quality preservation of plant cell structure. Tissues used were: internodes of Chara vulgaris, leaves of Hordeum vulgare, root tips of Lepidium sativum. Microwave irradiation was done with a commercial microwave oven (Sharp R-5975). Fixatives used were: 2.5% glutaraldehyde in 0.1 M sodium cacodylate buffer, pH 7.2 and 1% osmium tetroxide in veronal/acetate buffer, pH 7.2. Conventional fixations with glutaraldehyde/osmium were compared with microwave fixations. Examinations of thin sections showed that microwave fixation (glutaraldehyde or sequential aldehyde/osmium) is an attractive and rapid alternative method for processing plant tissues for electron microscopy. The optimal conditions found were: microwave oven at power level 50 W, 6.5 ml of fixative solution, irradiation times between 32–34 s, final temperature between 40° C and 47° C.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Argall K, Armati P (1990) Use of microwave fixation in the preparation of cell culture for observation with the scanning electron microscope. J Electron Microsc Tech 16:347–350

    Google Scholar 

  • Barton R (1965) Electron microscope studies on surface activity in cells of Chara vulgaris. Planta 66:95–105

    Google Scholar 

  • Benhamou NS, Noel S, Grenier J, Asselin A (1991) Microwave energy fixation of plant tissue: an alternative approach that provides excellent preservation of ultrastructure and antigenicity. J Electron Microsc Tech 17:81–94

    Google Scholar 

  • Boon ME, Kok LP (1987) Microwave cookbook of pathology. The art of microscopical visualization. Coulomb Press, Leyden

    Google Scholar 

  • Crawley JCW (1965) A cytoplasmic organelle associated with the cell walls of Chara and Nitella. Nature 205:200–201

    Google Scholar 

  • Forsberg C (1965) Naturitional studies of Chara in axenic cultures. Physiol Plant 18:275–290

    Google Scholar 

  • Heumann H-G (1987) Effects of heavy metals on growth and ultrastructure of Chara vulgaris. Protoplasma 136:37–48

    Google Scholar 

  • Hillmer S, Joachim S, Robinson DG (1991) Rapid polymerisation of LR-White for immunocytochemistry. Histochemistry 95:315–318

    Google Scholar 

  • Hopwood D, Coghill G, Ramsay J, Milne G, Kerr M (1984) Microwave fixation: its potential for routine technique, histochemistry, immunocytochemistry and electron microscopy. Histochem J 16:1171–1191

    Google Scholar 

  • Jensen FE, Harris KM (1989) Preservation of neuronal ultrastructure in hippocampal slices using rapid microwave-enhanced fixation. J Neurosci Methods 29:217–230

    Google Scholar 

  • Kang Z, Rohringer R, Chong J, Haber S (1991) Microwave fixation of rust-infected wheat leaves. Preservation of fine structure and detection of cell surface antigens, lectin-binding, and sugarbinding sites. Protoplasma 162:27–37

    Google Scholar 

  • Leong ASY, Daymon ME, Milios J (1985) Microwave irradiation as a form of fixation for light and electron microscopy. J Pathol 146:313–321

    Google Scholar 

  • Leong ASY, Milios J (1986) Rapid immunoperoxidase staining of lymphocyte antigens using microwave irradiation, J Pathol 148:183–187

    Google Scholar 

  • Login GR, Dvorak AM (1985) Microwave energy fixation for electron microscopy. Am J Pathol 120:230–243

    Google Scholar 

  • Login GR, Dvorak AM (1988) Microwave fixation provides excellent preservation of tissue, cells and antigens for light and electron microscopy. Histochem J 20:373–387

    Google Scholar 

  • Login GR, Dwyer BK, Dvorak AM (1990) Rapid primary microwave-osmium fixation. I. Preservation of structure for electron microscopy in seconds. J Histochem Cytochem 38:755–762

    Google Scholar 

  • Login GR, Stavinoha WB, Dvorak AM (1986) Ultrafast microwave energy fixation for electron microscopy. J Histochem Cytochem 34:381–387

    Google Scholar 

  • Nagai R, Rebhun LI (1966) Cytoplasmic microfilaments in streaming Nitella cells. J Ultrastruct Res 14:571–589

    Google Scholar 

  • Pickett-Heaps JD (1967) Ultrastructure and differentiation in Chara sp. I. Vegetative cells. Aust J Biol Sci 20:539–551

    Google Scholar 

  • Volkmann D, Sievers A (1979) Graviperception in multicellular organs. In: Haupt W, Feinleib ME (eds) Physiology of movements. N S 7. Springer, Berlin Heidelberg New York, pp 573–600

    Google Scholar 

  • Walsh GE, Bohannon PM, Wessinger-Duvall PB (1989) Microwave irradiation for rapid killing and fixing of plant tissue. Can J Bot 67:1272–1274

    Google Scholar 

  • Wild P, Krähenbühl M, Schraner EM (1989) Potency of microwave irradiation during fixation for electron microscopy. Histochemistry 91:213–220

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Heumann, HG. Microwave-stimulated glutaraldehyde and osmium tetroxide fixation of plant tissue: ultrastructural preservation in seconds. Histochemistry 97, 341–347 (1992). https://doi.org/10.1007/BF00270036

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00270036

Keywords

Navigation