Protoplasma

, Volume 141, Issue 1, pp 47–55

Preparation and properties of pollen sporoplasts

Authors

  • B. G. Baldi
    • Graduate Program in Plant PhysiologyWashington State University
    • Institute of Biological ChemistryWashington State University
  • V. R. Franceschi
    • Department of BotanyWashington State University
  • F. A. Loewus
    • Institute of Biological ChemistryWashington State University
Review Article

DOI: 10.1007/BF01276787

Cite this article as:
Baldi, B.G., Franceschi, V.R. & Loewus, F.A. Protoplasma (1987) 141: 47. doi:10.1007/BF01276787

Summary

Methods for the removal of exine from mature, ungerminatedLilium longiflorum pollen and release of intact gametophytes (sporoplasts) have been developed. These methods rely on the low temperature solvolytic activity of 4-methylmorpholine N-oxide (MMNO), which allows partial or complete detachment of exine from intine during subsequent washing procedures. These methods are: aqueous MMNO combined with cyclohexylamine (method I), aqueous MMNO at alkaline pH (method II), and aqueous MMNO containing a high Ca2+ concentration with added cellulysin and macerase (method III). Sporoplasts produced by methods I and II are most frequently completely separated from exine and, as shown by histochemical tests, enveloped by the intine layer. Selected enzyme activities in method II sporoplasts are measurable but, as indicated by other tests, considerable damage to the plasma membrane accompanies this treatment. Sporoplasts produced by melhod III largely remain attached to their ruptured exine layer and retain substantial biological competence in terms of extractable enzyme activities, membrane integrity, and respiration.

Keywords

Lilium longiflorum 4-Methylmorpholine N-oxide Pollen exine Sporoplast

Abbreviations

MMNO

4-methylmorpholine N-oxide

SEM

scanning electron microscope

TEM

transmission electron microscope

Copyright information

© Springer-Verlag 1987