Cell cycle activity in dry and germinating untreated and treated (soaked in
water and subsequently in fungicide) seeds of two sugarbeet cultivars, col
lected at commercial harvest time (late mature seeds) and about 2 weeks bef
ore this (immature seeds), was investigated by flow cytometry, and by immun
e-detection of beta-tubulin and the B-subunit of the 11 S globulin. Germina
tion capacity and field emergence were tested. With dry seeds of both culti
vars, higher G(2)/G(1) ratios were observed in the radicle tips of late mat
ure seeds, as compared with those from immature seeds. The late mature seed
s contained more partly degraded (soluble) B-subunit of 11 S globulin, typi
cal of germinating or primed sugarbeet seeds. Thus events associated with t
he onset of germination had occurred in the seed lots collected at commerci
al harvest time. The cytoskeleton protein beta-tubulin was not detectable i
n dry seeds from either harvest. Western blotting revealed an accumulation
of beta-tubulin during germination and this was faster in the late mature h
arvested seeds which was correlated with the onset of DNA replication. Soak
ing enhanced the rate of cell cycle activation during germination as well a
s vigour, germination capacity, and field emergence. There was positive cor
relation between the G(2) / G(1) ratio and the traits examined in laborator
y and field tests. It is concluded that a combined analysis of proteins and
cell-cycle-related events can be used in understanding and predicting suga
rbeet seed quality.