The aim of this work was to discover why barley (Hordeum vulgare L.) m
icrospores die when cultured on media containing 40 mM sucrose but und
ergo embryogenesis on 40 mM maltose. Freshly isolated microspores were
cultured for 6-24 h on media containing either [U-C-14] maltose or [U
-C-14] sucrose at 40 mM, and the detailed distribution of C-14 was det
ermined. The amounts of glycolytic intermediates, ATP, ADP and AMP, in
microspores were also measured. Cultures on sucrose differed from tho
se on maltose in that the initial rate of metabolism was faster but de
clined rapidly, less C-14 was recovered in polymers and more in alanin
e, there was extensive leakage of assimilated carbon, significant accu
mulation of ethanol and a lower adenylate energy charge. It is argued
that microspores cultured on 40 mM sucrose die because they metabolize
the sugar rapidly, become hypoxic and, as a result, accumulate large
quantities of ethanol within the cells. Metabolism of maltose is slowe
r and there is sufficient oxygen available to allow cells to survive i
n culture. Consequently some of the cultured cells undergo embryogenes
is.