Nuclear staining was carried out by the method of Slater (1976) with the following modifications. Chromomycin A3 (Sigma) was used instead of mithramycin and it was found necessary to fix protoplast preparations before staining. Protoplasts were fixed in 4 % (v/v) glutaraldehyde in 0.8 M mannitol for 1.5h at room temperature. The fixative was removed by centrifugation and the pellet resuspended in distilled water. An equal volume of the stain (0.4 mg ml^-1 chromomycin in 50 % aqueous ethanol containing 30 mM MgCl₂) was then added and the material examined as a wet mount. Whole mycelium was also stained to investigate the distribution of nuclei in hyphae. No fixation was required and washed mycelium was mounted in the stain. To reveal septa the preparations were counterstained with 0.0005 % (v/v) aqueous Tinopal (Ciba-Geigy). All the samples were examined under a Vickers M17 uv-fluorescence microscope containing the following filters:

Photographs were taken using Ilford HP5 (400 ASA) film. Storage of the stained material at 4^oC for 24h improved the staining.

Reference

Slater, M. L. (1976). Rapid nuclear staining method for Saccharomyces cerevisiae. Journal of Bacteriology, 126, 1339-1341.

(1) Hypha of C. acremonium stained with Chromomycin and Tinopal, showing nuclei and septa. The uninucleate nature of the hyphal compartments in this organism are clearly illustrated.

(2) Protoplasts of C. acremonium stained with Chromomycin. The protoplasts were fixed in 0.8 M mannitol containing 4% glutaraldehyde prior to staining. Note the rare binucleate protoplast.

(3) Hypha of A. nidulans stained with Chromomycin and Tinopal. Note the multinucleate hyphal tip.

The bar markers represent 10 microns.