Mouse oocytes and zygotes, when solubilised demonstrated that a range
of ketoaldehydes could be utilised as substrates. Of the five ketoalde
hydes investigated the overall substrate utilisation was hydroxypyruva
te > glyoxylate > 2-ketobutyrate > pyruvate > glycolate. The utilisati
on of these ketoaldehydes during early development by LD-I may provide
a source of new metabolic substrates in addition to the potential con
trol of aldehyde toxicity. It is proposed therefore that the LD-1 isoe
nzyme is responsible for ketoaldehyde utilisation prior to implantatio
n thereby providing a source of alternative metabolic substrates for t
he developing embryo.