S U M M A R YGerm-tube emergence in Aspergillus nidulans exhibits partial synchrony. Germ tubes were first detected at 210 min. after inoculation of spores into a liquid medium. Almost all spores produced germ tubes within 360 min., 4 9 3 % of them doing so between 240 and 300 min. Increase in dry weight was first detected at 120 min. and various constituents at the following times: RNA (30 min.), Kjeldahl nitrogen (30 min.), protein (150 min.) and DNA (180 min.). Pauses in the increase of DNA, RNA and protein were observed. The DNA content per nucleus during the first replication cycle reached twice that of the resting spore, but at later stages of germination values only 10 % higher were observed. Spores containing 2, 4 and 8 nuclei were first detected at 270, 390 and 480 rnin. respectively. Caten, 1969). The present work was undertaken to study nuclear division and macromolecular synthesis during spore germination.
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METHODSOrganisms. Strain BWB 50 bi I ; w 3 was used throughout this work. The strain, which has white spores and requires biotin, was originally obtained from Glasgow University.Preparation of spore suspensions. Thirty ml. volumes of complete medium agar (MacKintosh & Pritchard, 1963) in 250 ml. conical flasks were inoculated with a spore suspension and incubated at 37" for 7 days. The spores were harvested by adding 20 ml. of 0-1 % (v/v) Tween 80 together with sterile glass beads or marbles. The flasks were agitated and the spore suspensions removed under aseptic conditions and pooled. Spore chains were broken with a Rotamixer (Hook & Tucker Ltd) and hyphal fragments removed by filtration through six layers of sterile muslin. The spores were washed twice and suspended in sterile distilled water. Spore counts were made with a Fuchs-Rosenthal haemocytometer slide, at least 300 spores being counted. Spores thus prepared had a viability of 95 to 99 % after storage at 4" for several days, although the experiments reported here were carried out within 24 h.Cultural conditions and media. Spores were added to 400 ml. of liquid DAN medium containing 50 pg./l. biotin (Trinci, 1969) in a 2 1. conical flask to give a concentration of
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