1) The oxygen consumption increases during Bufo bufo development in accorda
nce with the two steps which border at the "heart beat" stage 2) Cytochrome
c oxidase activity is not proportional to the oxygen consumption: it is no
table and constant in the first step, and it only increases in the second 3
) In the mitochondria of preneural embryos, citrate synthase, NADP(+) depen
dent isocitrate dehydrogenase, and succinate dehydrogenase activities are v
ery low in respect to malate dehydrogenase and glutamate oxaloacetate trans
aminase activities. The Krebs cycle results lowered at the condensing react
ion level with acetyl accumulation when pyruvate is available. The same beh
avior has been observed in the Xenopus laevis oocytes and differentiated ti
ssues. 4) The presence of a phosphagen system which is different from creat
ine phosphate and arginine phosphate, supporting ATP level, has been demons
trated in B. bufo embryos. 5) Mitochondria of portneural embryos are able t
o accomplish a complete Krebs cycle by increasing citrate synthase, and suc
cinate dehydrogenase activities. 6) In all B. bufo development malate dehyd
rogenase and glutamate oxaloacetate transaminase constitute a multienzymati
c system by which the mitochondria accomplish a decarboxylic amino acid shu
nt required for the transformation of deutoplasm into protoplasm. This shun
t is also operative in the X. laevis oocytes. 7) Through pyruvate productio
n, by oxidative decarboxylation of malate, the NAD(P)(+) dependent malic en
zyme could carry out a fundamental anaplerotic function in the mitochondria
which is specialized in the production of biosynthetic blocks belonging to
the embryo in which the carbohydrates metabolism rather than the glycolyti
c activity is designed for pentose phosphate and glycerol phosphate synthes
is for protein and cytomembrane production. 8) Consistent metabolic differe
nces have been highlighted between B. bufo embryos and X. laevis embryos.